accession
stringlengths 6
10
| embedding
sequencelengths 128
128
| protein_name
stringlengths 2
149
| organism_name
stringlengths 7
183
| ncbi_taxonomy_class
stringclasses 263
values | ncbi_taxonomy_phylum
stringclasses 117
values | gene_name
stringlengths 1
43
⌀ | sequence_length
int64 2
3k
| protein_existence
int64 1
5
| sequence_version
int64 1
9
| ncbi_taxonomy_id
int64 14
3.35M
| organism_identifier
int64 14
3.04M
| function
stringlengths 5
12.4k
⌀ | sequence
stringlengths 2
3k
|
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Q8DRY7 | [
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] | Zinc transporter ZupT | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | Bacilli | Bacillota | zupT | 264 | 3 | 1 | 210,007 | 210,007 | Mediates zinc uptake. May also transport other divalent cations | MSQHLFTAFILTALAGLSTGIGSLIAFVTKHTNKTFLSVSLGFSAGVMIYVSMIEIFPTAQTILTKAMDKKSGSWLTVLAFFGGILLIAIIDKLIPSEENPHEIKTIEEEDQKPTKLMRMGLMTAIAIGIHNFPEGLATFISGLQDASIAIPIVIAIAIHNIPEGIAVSVPIYQATGSKKKAFTYSFLSGLAEPLGAIIGWFLLMPIMNNIVYGAIFSAVAGIMVFISLDELLPAAEEYGKHHLAIYGVISGMLIMAVSLLLFI |
Q8PKQ5 | [
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] | Zinc transporter ZupT | Xanthomonas axonopodis pv. citri (strain 306) | Gammaproteobacteria | Pseudomonadota | zupT | 272 | 3 | 1 | 190,486 | 190,486 | Mediates zinc uptake. May also transport other divalent cations | MLAVSSHNLWIALAVTLAAGLATGLGSLMVVFAKKPNPRLLAFGLAFAGGAMVYVSLTEILNKSIAAFSQAYNDKLGFTFGTLTFLGGMLLIMVIDRLVPNPHQSLSSDDPQFREDNRAYIRRVGLMTAVAITAHNFPEGLATFFATLESPAVGMPLAFAIAIHNIPEGIAIAVPVYFATRNKFYAVGASLLSGLAEPVGAGIGYLALFSVLSDAVFGTVFGLISGVMVFLALDELLPAAKRYAQGHETVYGLVSGMGTLAISLVLFRFATP |
Q8P8Z6 | [
0.09450880438089371,
0.021171951666474342,
0.1222127303481102,
0.058576181530952454,
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] | Zinc transporter ZupT | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | Gammaproteobacteria | Pseudomonadota | zupT | 272 | 3 | 1 | 190,485 | 190,485 | Mediates zinc uptake. May also transport other divalent cations | MLEVSSHNVWTALAVTLAAGLATGLGSLMVVFAKKPNPRLLAFGLAFAGGAMVFVSLSEILNKSIASFSNAYNDKLGFTYGTLTFLGGMLLIMVIDRLVPNPHQSLSTDDPQFRDDNRAYIRRVGLLTAVAITAHNFPEGLATFFATLESPAVGMPLAFAIAIHNIPEGIAIAVPVYFATRNKFYAFGASLLSGLAEPIGAGIGYLLLSSVLSEAVFGAVFGVIAGVMVFLALDELLPAAKRYAQGHETVYGLVSGMGTLAISLVLFRYAAP |
Q926D8 | [
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0.016900209710001945
] | Zinc uptake system ATP-binding protein ZurA | Listeria innocua serovar 6a (strain ATCC BAA-680 / CLIP 11262) | Bacilli | Bacillota | zurA | 257 | 3 | 1 | 272,626 | 272,626 | Involved in a zinc uptake transport system | MNKIIEVNNVSYHYDKEHALENIHFQVEKGSFTGLIGPNGSGKSTMLKLILGVLKKQQGSIALFGEKQADFKDWVKIGFVSQKSNAFNSAFPATVKEVVASGLTKKKGLFKTLNNQDKEAIDYALKRVEMTDYLHRNIGELSGGQQQRVFIARALVSRPELLILDEPTVGVDVENVKAFYELLAELNRTEEMTLLLVTHDLVAVNTYVNHVISINKRIIFDGSAHEYQHYLADRELEILAEQRRREDACLDCDASPV |
Q9XDA6 | [
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] | Zinc uptake system ATP-binding protein ZurA | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | Bacilli | Bacillota | zurA | 257 | 3 | 1 | 169,963 | 169,963 | Involved in a zinc uptake transport system | MKKIIEVNNVSYHYDKEHALENIHFQVAKGSFTGLIGPNGSGKSTMLKLILGVLKKQQGSISLFGEKQADFKDWVKIGFVSQKSNAFNSAFPATVKEVVASGLTKKKGLFKTLNNKDKEDIDYALKRVEMTDYLHRNIGELSGGQQQRVFIARALVSRPELLILDEPTVGVDVENVKAFYELLAELNRTEEMTLLLVTHDLMAVNTYVNHVISINKRIIFDGSAHEYQHYLADRELEILAEQRRREDACLDCDASPV |
P0A3E7 | [
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] | Transcriptional regulator ZurR | Listeria innocua serovar 6a (strain ATCC BAA-680 / CLIP 11262) | Bacilli | Bacillota | zurR | 141 | 3 | 1 | 272,626 | 272,626 | Probably required for the zinc-specific repression of the operon zuRMA implicated in zinc uptake | MGLTATEALMKMKEKGYKHTDKREFLINLLARKNKYLTAKDVLENMKDDFPGISFDTIYRNLSLFVELGIFEETDLSGERNFRLACTHEHHHHHFICMKCGKTKEIMMCPMDFLTEALPGYQIDGHKFEVYGECPECLQAS |
P0A3E6 | [
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] | Transcriptional regulator ZurR | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | Bacilli | Bacillota | zurR | 141 | 3 | 1 | 169,963 | 169,963 | Probably required for the zinc-specific repression of the operon zuRMA implicated in zinc uptake | MGLTATEALMKMKEKGYKHTDKREFLINLLARKNKYLTAKDVLENMKDDFPGISFDTIYRNLSLFVELGIFEETDLSGERNFRLACTHEHHHHHFICMKCGKTKEIMMCPMDFLTEALPGYQIDGHKFEVYGECPECLQAS |
P54479 | [
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] | Zinc-specific metallo-regulatory protein | Bacillus subtilis (strain 168) | Bacilli | Bacillota | zur | 145 | 1 | 2 | 224,308 | 224,308 | Acts as a negative controlling element, employing Zn(2+) as a cofactor to bind the operator of the repressed genes. Required for the zinc-specific repression of two operons implicated in zinc uptake, yciC and ycdHIyceA. Also represses the expression of rpmE2, the gene for ribosomal protein L31B, which is expressed only after the end of exponential growth | MNVQEALNLLKENGYKYTNKREDMLQLFADSDRYLTAKNVLSALNDDYPGLSFDTIYRNLSLYEELGILETTELSGEKLFRFKCSFTHHHHHFICLACGKTKEIESCPMDKLCDDLDGYQVSGHKFEIYGTCPDCTAENQENTTA |
P0AC51 | [
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] | Zinc uptake regulation protein | Escherichia coli (strain K12) | Gammaproteobacteria | Pseudomonadota | zur | 171 | 1 | 1 | 83,333 | 83,333 | Acts as a negative controlling element, employing Zn(2+) as a cofactor to bind the operator of the repressed genes (znuACB) | MEKTTTQELLAQAEKICAQRNVRLTPQRLEVLRLMSLQDGAISAYDLLDLLREAEPQAKPPTVYRALDFLLEQGFVHKVESTNSYVLCHLFDQPTHTSAMFICDRCGAVKEECAEGVEDIMHTLAAKMGFALRHNVIEAHGLCAACVEVEACRHPEQCQHDHSVQVKKKPR |
P9WN84 | [
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] | Zinc uptake regulation protein | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | Actinomycetes | Actinomycetota | zur | 130 | 3 | 1 | 83,331 | 83,331 | Global transcriptional regulator involved in zinc homeostasis | MSAAGVRSTRQRAAISTLLETLDDFRSAQELHDELRRRGENIGLTTVYRTLQSMASSGLVDTLHTDTGESVYRRCSEHHHHHLVCRSCGSTIEVGDHEVEAWAAEVATKHGFSDVSHTIEIFGTCSDCRS |
P9WN85 | [
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] | Zinc uptake regulation protein | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | Actinomycetes | Actinomycetota | zur | 130 | 1 | 1 | 83,332 | 83,332 | Global transcriptional regulator involved in zinc homeostasis. Represses the transcription of at least 32 genes, including genes involved in zinc homeostasis, by binding to promoter sequences that contain a conserved 26 bp palindrome, in the presence of zinc | MSAAGVRSTRQRAAISTLLETLDDFRSAQELHDELRRRGENIGLTTVYRTLQSMASSGLVDTLHTDTGESVYRRCSEHHHHHLVCRSCGSTIEVGDHEVEAWAAEVATKHGFSDVSHTIEIFGTCSDCRS |
P0AC52 | [
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] | Zinc uptake regulation protein | Shigella flexneri | Gammaproteobacteria | Pseudomonadota | zur | 171 | 3 | 1 | 623 | 623 | Acts as a negative controlling element, employing Zn(2+) as a cofactor to bind the operator of the repressed genes (znuACB) | MEKTTTQELLAQAEKICAQRNVRLTPQRLEVLRLMSLQDGAISAYDLLDLLREAEPQAKPPTVYRALDFLLEQGFVHKVESTNSYVLCHLFDQPTHTSAMFICDRCGAVKEECAEGVEDIMHTLAAKMGFALRHNVIEAHGLCAACVEVEACRHPEQCQHDHSVQVKKKPR |
O48626 | [
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] | Centromere/kinetochore protein zw10 homolog | Arabidopsis thaliana | Magnoliopsida | Streptophyta | ZW10 | 742 | 1 | 1 | 3,702 | 3,702 | May be required for accurate chromosome segregation. Required for proper maturation of seed storage proteins. Forms a complex with MAG2, MIP2 and MIP3 on the endoplasmic reticulum that may be responsible for efficient transport of seed storage proteins | MPEIDALFESINVRDLLAGHDLNDPTTPLSAPDLRLLINRLESHSLRIKSKVQSYLVAHHSDFSELFSLCQDTVSRTRLISDDVSDVLQLVSDRPIDVEIRSVVDEITEKTKEVKLKRESLDLVNAIVGICEALQETKEALKNGRFRFAAERIRELKVVLRIGEEEDGEPVAYALLRKEWSNCFDEIQEVLAKFMENAVRFELDSSRIRIKYQLSVGETAGIALSTVLEAMEVIGILDYGLAKAADSIFKHVITPAVTHASTFAAVEDLCKSAGEVTEATLRLEQSSDHKFEDVDGDAMYSGILKVVKFICSSLCFGNVTWIHSFGRLTWPRISELIISKFLSKVVPEDASKLADFQKIIERTSQFEAALKELNFVSSSDAESRLSKYAEDVEVHFASRKKIEILAKARNLLLQCNFTIPQDIAMRNAKHIVCLLFSSERCVVSEAASQLMNLVHKTLEDVCVSSARVASEFYNAARDSILLYEAVVPVKLEKQLDGLNEAAVLLHNDCLYLFEEILGLAFEYRASFPSSIKEYAVFADIAPRFKLMAEEVLQKQVHLVISSLREAIDSADGFQNTHQIKQFKSAEFSIDQVVFSLKNVHMIWEPVLRPKTYKQSMCAVLESVFRRIARDILLLDDMAADETFELQKLIYLMLKNLSSVLDSVRSADETSRPLDDIIPSLRKTRKLAELLDMPLMSITSAWESGELFRCNFTRTEVQDFIKAIFTDSPLRKECLWRIDEVNQ |
Q19642 | [
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] | Centromere/kinetochore protein zw10 homolog | Caenorhabditis elegans | Chromadorea | Nematoda | czw-1 | 778 | 1 | 1 | 6,239 | 6,239 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis (PubMed:9298984). Required for the assembly of the dynein-dynactin and mdf-1-mdf-2 complexes onto kinetochores (PubMed:18936247). Its function related to the spindle assembly machinery and kinetochore-microtubule attachments likely depends on its association in the mitotic RZZ complex (PubMed:18936247). The RZZ complex recruits the spindly-like protein spdl-1 to kinetochores (PubMed:18765790, PubMed:18936247). To prevent irregular chromosome segregation, the complex also inhibits the attachment of the kinetochore-associated NDC80 complex to microtubules (PubMed:24231804). The recruitment of spdl-1 to kinetochores relieves this inhibition (PubMed:24231804). Required for embryonic development (PubMed:9298984) | MASSEGSYRDLEKKLKNGLTSISQDIVDKYGNLKVSLNVNATAKLIFDRLENLEDIAEMSTRNLSNLIDQTAKDSPEMLAEIKSQAQSCENLVEFLQSMKNVEEQLIIMRSKTTNRVEWGTAILACKDFLNDTNMLLEGIGRDGFDMSVPLKHFAAEYSVLSYNCRYQLSADYERAMNVPKLSKQKCGDRTNVSFSVFNVGSVEDQKMLNETLSAMNMIGQLPERLDAWKIVILNVFCEAIVASRDGVDVYIVDNPTPDQTRFLINQKPRGKKDKTIDVAKVLESMEVFFTKLHSVLHSHELLDATGKTFTSMIGSVIEEQLITMILKDVIAIAAPVTETADEDQEMFINLLQIGEVFVERMKELGFFSQKAKLLFTLDTDTIFVTRRCFAIVSKANKLINETYDKLVTVGVDDSAIKDIDLLAKAHTHAEHFAKEYGKDLGRLWSHNEDSQFPSFFAFQKCTVSESTINFVNLLRDNVKAAFACEDEGARAKLALTAENIVRLYVILTPRKHAELFSSIPNMAAIFYNNCHYISHCIMTMSFEASGDNQKTLLEPLLLDSVIRLRTVAADCMEKTLTRCRREMTAYLEDHSIFEHLPASYKTTKNTFAAAEEMSESADILVPREEPKIIKCLAACLLHIRLIAKNLREPLTEVVYCKVIGSLVSFLLDSLVRHVVTTSDFRENDANVMADVFKRLLEVVANIVAYKEQTKVTDFCAREYFRLNEIVFVLGNRMQDIEHRWFNAKGPMAEHLSRSEVVGLIKALFADSQHRSDLIARL |
O44219 | [
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] | Centromere/kinetochore protein zw10 | Drosophila grimshawi | Insecta | Arthropoda | mit(1)15 | 714 | 3 | 1 | 7,222 | 7,222 | Required for accurate chromosome segregation | MAETQVLLETYQGQGNNNATNIEATKAAIKKMLVRIERFQTRVRKHIDENYVDFMPNHTSPDIFLEKSSALGDEISDLLATVGNEGLSVLSDASVELAALSRDLREKLFGLRVSEHILKLDDLFQCVEEAKSTKDCLVVLDLMGRLRSLIYGEGTSDDISPDVERIFQSLECYESIKVKYHVQAHLLQQNLQERFDRLVQLSCKSFPTSKCVTLLISKDEALLQDIVIALFQESYNPTKLCAFLLENCIEPLIQKPVSVEYNVNAKDGTHIQLTLSYSIKEPDTSSLLRPNYKDVFEHFRLLLKTLCGINSSLNGTQHVFTVIGDHVKERMLQLLLDECLIRVPETMDEYNSSTLCEDVAEFEHQLVDTFLINPELDTTLTEFTKQFDTYYRNRLSERVLATAREIIQRDLQDMTLVAPSNLSANVASDPLLFPRCMVSKSAQVDFVKLMERVVRQPDKAAEGTPDPLGGVIGLLLDAYINEVPKVHKKLLKSIPQQSALFYNNCMYLTHWVAQHTKDNIDGFPSLVKILQSTGNKHLRVQVSYQESILMDIMSSFEFENPHTLGTAPLRLVRQCLRQLELLKNVWQQVPAENVYNNSFCELLQAFINELVQRVFSLRDISATMASELSDLIDVVLEKASILFHDKNDVVHVRSWLKLQQLKIMMNASLKEFSELWCDGVGPLTANYHADEIKHLIRALFQDTDRRAKAITQIV |
Q9W4X9 | [
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] | Centromere/kinetochore protein zw10 | Drosophila melanogaster | Insecta | Arthropoda | Zw10 | 721 | 1 | 2 | 7,227 | 7,227 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis (PubMed:15886105, PubMed:17576797). Required for the assembly of the dynein-dynactin, Mad2 complexes and spindly/CG15415 onto kinetochores (PubMed:15886105, PubMed:17576797). During cytokinesis in male meiotic cells it is required for completion of cleavage furrow ingression, possibly in conjunction with Rint1 (PubMed:22685323). Required for maintenance of Golgi stack number and morphology, and acroblast assembly (PubMed:22685323). Its function related to the spindle assembly machinery is proposed to depend on its association in the RZZ complex (PubMed:22685323). Failure to assemble the complex due to the absence of any one of its components, results in the incorrect redistribution of the remaining components to diverse membrane compartments (PubMed:22685323) | MEEEAPRFNVLEEAFNGNGNGCANVEATQSAILKVLTRVNRFQMRVRKHIEDNYTEFLPNNTSPDIFLEESGSLNREIHDMLENLGSEGLDALDEANVKMAGNGRQLREILLGLGVSEHVLRIDELFQCVEEAKATKDYLVLLDLVGRLRAFIYGDDSVDGDAQVATPEVRRIFKALECYETIKVKYHVQAYMLQQSLQERFDRLVQLQCKSFPTSRCVTLQVSRDQTQLQDIVQALFQEPYNPARLCEFLLDNCIEPVIMRPVMADYSEEADGGTYVRLSLSYATKEPSSAHVRPNYKQVLENLRLLLHTLAGINCSVSRDQHVFGIIGDHVKDKMLKLLVDECLIPAVPESTEEYQTSTLCEDVAQLEQLLVDSFIINPEQDRALGQFVEKYETYYRNRMYRRVLETAREIIQRDLQDMVLVAPNNHSAEVANDPFLFPRCMISKSAQDFVKLMDRILRQPTDKLGDQEADPIAGVISIMLHTYINEVPKVHRKLLESIPQQAVLFHNNCMFFTHWVAQHANKGIESLAALAKTLQATGQQHFRVQVDYQSSILMGIMQEFEFESTHTLGSGPLKLVRQCLRQLELLKNVWANVLPETVYNATFCELINTFVAELIRRVFTLRDISAQMACELSDLIDVVLQRAPTLFREPNEVVQVLSWLKLQQLKAMLNASLMEITELWGDGVGPLTASYKSDEIKHLIRALFQDTDWRAKAITQIV |
O44218 | [
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] | Centromere/kinetochore protein zw10 | Drosophila pseudoobscura pseudoobscura | Insecta | Arthropoda | mit(1)15 | 718 | 3 | 2 | 46,245 | 46,245 | Required for accurate chromosome segregation | MAARAQIKLLPEMFQSNGCASLEDTKSTVSKVQTRTERFQERVRKHIDENYSEFMTNHTSPDIFLEESSSLGREINDLLETVGTEGLAALNGSSTQLADHSRELRELMLGLQVSEHILKIDELFQCVEEAKGTKDYLVVLDLVGRLRSLIYGEGEAATQDVVRIFQALECYETIKVKYHVQAHLLQQNMQERFDRLVQLNCKSFPNSKCVTLLVSKEEGQLHDIVIALFQERYNPVRLCEFLLENCIEPLILKPVGVECNENAEAGTYVQLSLSYSTKESGTASGTSTQLRPNYKQVLEHFRLLLQTLSGINHSLSSSQHVFSIIGDHVKDRMMHLLVNDCLIPAVPETMEEYQASTLCEDVAHFEQYLADSFLINPEVDRGLSQFIEQYGTYYRNRLCSRVLESTREIIQRDLQDMVLVAPNNQAMDVTGCDPFLFPRCMVSRSAQDFMKLMERILRQPTEKPGEDEADPLAGVIGMMLQTYIDEVPKVHKKLLESIPQQSVLFHNNCMYFTHWVAQNANKGIESFPALVKTLQATGTMHFRVQVTYQTSILMDIMESFEFESPHTLGTGPLKLVRQCLRQLELLKNVWQNVLPDNVYNSTFVELLHAFINELVRHIFTQRDISATMASDLSDLIDVVLEKAPKLFRDPHEVHQVRSWMKLQQLKTMMNASLKEITELWCKGAGPLTANYKADEIRYLIRALFQDTDRRAKAITQIM |
O43264 | [
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] | Centromere/kinetochore protein zw10 homolog | Homo sapiens | Mammalia | Chordata | ZW10 | 779 | 1 | 3 | 9,606 | 9,606 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex (PubMed:11590237, PubMed:15485811, PubMed:15824131). Involved in regulation of membrane traffic between the Golgi and the endoplasmic reticulum (ER); the function is proposed to depend on its association in the interphase NRZ complex which is believed to play a role in SNARE assembly at the ER (PubMed:15029241) | MASFVTEVLAHSGRLEKEDLGTRISRLTRRVEEIKGEVCNMISKKYSEFLPSMQSAQGLITQVDKLSEDIDLLKSRIESEVRRDLHVSTGEFTDLKQQLERDSVVLSLLKQLQEFSTAIEEYNCALTEKKYVTGAQRLEEAQKCLKLLKSRKCFDLKILKSLSMELTIQKQNILYHLGEEWQKLIVWKFPPSKDTSSLESYLQTELHLYTEQSHKEEKTPMPPISSVLLAFSVLGELHSKLKSFGQMLLKYILRPLASCPSLHAVIESQPNIVIIRFESIMTNLEYPSPSEVFTKIRLVLEVLQKQLLDLPLDTDLENEKTSTVPLAEMLGDMIWEDLSECLIKNCLVYSIPTNSSKLQQYEEIIQSTEEFENALKEMRFLKGDTTDLLKYARNINSHFANKKCQDVIVAARNLMTSEIHNTVKIIPDSKINVPELPTPDEDNKLEVQKVSNTQYHEVMNLEPENTLDQHSFSLPTCRISESVKKLMELAYQTLLEATTSSDQCAVQLFYSVRNIFHLFHDVVPTYHKENLQKLPQLAAIHHNNCMYIAHHLLTLGHQFRLRLAPILCDGTATFVDLVPGFRRLGTECFLAQMRAQKGELLERLSSARNFSNMDDEENYSAASKAVRQVLHQLKRLGIVWQDVLPVNIYCKAMGTLLNTAISEVIGKITALEDISTEDGDRLYSLCKTVMDEGPQVFAPLSEESKNKKYQEEVPVYVPKWMPFKELMMMLQASLQEIGDRWADGKGPLAAAFSSSEVKALIRALFQNTERRAAALAKIK |
O54692 | [
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] | Centromere/kinetochore protein zw10 homolog | Mus musculus | Mammalia | Chordata | Zw10 | 779 | 1 | 3 | 10,090 | 10,090 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex. Involved in regulation of membrane traffic between the Golgi and the endoplasmic reticulum (ER); the function is proposed to depend on its association in the interphase NRZ complex which is believed to play a role in SNARE assembly at the ER (By similarity) | MASFVTEVLAHSGSLEKEDLGTRISRLTRRVEEIKGEVCNMISKKYSEFLPTMQSAQALVTQVDTLSNDIDQLKSRIETEVCRDLHISTVEFTNLKQQLERDSVVLTLLKQLQEFSSAIEEYNSALAEKKYIPAARHLEEAQECLKLLKSRKCFDLKMLKSLSMELTVQKQNILYHLGEDWQKLVVWKFPPAKDTSSLESCLQTELHLCTEQPEKEDMTPLPSISSVLLAFSILGELPTKLKSFGQMLLKYILKPLVTCPSLHAVIERQPSSVSICFESLTTDLEHPSPPEAFAKIRLVLEVLQKQLLDLPLDADLEIGKVPGIVLAEMLGEGIWEDLSECLIRNCLVYSIPTNSSKLQEYEEIIQSTEEFEKFLKEMRFLKGDTTDLLKYARNINSHFANKKCQDVIVAARNLMTSEIHNTVKIGPDCKEALPDLPSPDADHKLQVQTVCKAQFTDAGNLEPETSLDPQSFSLPTCRISEAVKKLMELAYQTLLEATTSSDQCAVQLFYSVRNIFHLFHDVVPTYHKENLRKLPQLAAIHHNNCMYIAHHLLTLGHQFRLRLAPILCDGTTTFVDLVPGFRRLGTECFLAQMQAQKGELLERLSSARSFANMDDEENYSAASKAVRQVLHQLRRLGIVWQDVLPVNIYCKAMGTLLNTAIAEMMSRITALEDISTEDGDRLYSLCKTVMDEGPQVFAPLSDENKNKKYQEEVPVYVSKWMPFKELMIMLQASLQEIGDRWADGKGPLATAFPSSEVKALIRALFQNTERRAAALAKIK |
Q5RFM4 | [
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] | Centromere/kinetochore protein zw10 homolog | Pongo abelii | Mammalia | Chordata | ZW10 | 779 | 2 | 3 | 9,601 | 9,601 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Involved in regulation of membrane traffic between the Golgi and the endoplasmic reticulum (By similarity) | MASFVTEVLAHSGRLEKEDLGARISRLTRRVEEIKGEVCNMISKKYSEFLPSMQSAQGLITQVDKLSEDIDLLKSRIESEVRRDLHVSTGEFTDLKQQLERDSIVLSLLKQLQEFSTAIEEYNCALTEKKYVTGAQRLEEAQKCLKLLKSRKCFDLKILKFLSMELTIQKQNILYHLGEEWQKLIVWKFSPSKDTSSLESYLQTELHLYTEQSHKEEKTPMPPISSVLLAFSVLGELHSKLKSFGQMLLKYILRPLASCPSLHAVIESQPNIVIIRFESIMTNLEYPSPSEVFTKIRLVLEVLQKQLLDLPLDTDLENEKTSTVPLAEMLGDMIWEDLSEYLIKNCLVYSIPTNSSKLQQYEEIIQSTEEFENALKEMRFLKGDTTDLLKYARNINSHFANKKCQDVIVAARNLMTSEIHNTVKIIPDSKINVPELPTPDEDNKLEVQKVSNTQYNEVMNLEPENTLDQHSFSLPTCRISESVKKLMELAYQTLLEATTSSDQCAVQLFYSVRNIFHLFHDVVPTYHKENLQKLPQLAAIHHNNCMYIAHHLLTLGHQFRLRLAPILCDGTATFVDLVPGFRRLGTECFLAQMRAQKGELLERLSSARNFSNMDDEENYSAASKAVRQVLHQLKRLGIVWQDVLPVNIYCKAMGTLLNTAISEVIGKITALEDISTEDGDRLYSLCKTVMDEGPQVFAPLSEESKNKKYQEEVPVYVPKWMPFKELMMMLQASLQEIGDRWADGKGPLAAAFSSSEVKALIRALFQNTERRAAALAKIK |
Q4V8C2 | [
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0.012984718196094036,
0.008110134862363338,
0.00863715074956417,
0.12944480776786804,
-0.0802566260099411,
0.002889445284381509,
0.006482375785708427,
0.14392715692520142,
-0.1341276615858078,
0.030926452949643135,
-0.03788280114531517,
0.033157799392938614,
-0.17646513879299164,
-0.08465094119310379,
-0.08214819431304932,
0.07513699680566788,
-0.15293742716312408,
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0.012423518113791943,
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0.20524750649929047,
0.12986987829208374,
-0.06786487251520157,
-0.0977589413523674,
-0.017316127195954323,
-0.05847178027033806,
0.06103372573852539,
0.05293282866477966,
-0.07015204429626465,
0.1947738081216812,
0.0769561156630516,
-0.05514054372906685,
-0.01684165745973587,
0.08465879410505295,
0.00586336012929678,
-0.009012180380523205,
0.060288719832897186,
0.012970717623829842,
0.05851732939481735,
-0.19234727323055267,
0.0994245633482933,
-0.03800441324710846,
-0.03233670815825462,
-0.10084716975688934,
0.14222070574760437,
-0.05999268591403961,
-0.0575026199221611,
0.08180404454469681,
-0.0693105086684227,
0.047863710671663284,
-0.04184512421488762,
-0.09804070740938187,
0.15418744087219238,
0.046293921768665314,
0.07864446192979813,
0.006359280087053776,
0.059791989624500275,
-0.13973763585090637,
-0.0886131227016449
] | Centromere/kinetochore protein zw10 homolog | Rattus norvegicus | Mammalia | Chordata | Zw10 | 777 | 2 | 3 | 10,116 | 10,116 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex. Involved in regulation of membrane traffic between the Golgi and the endoplasmic reticulum (ER); the function is proposed to depend on its association in the interphase NRZ complex which is believed to play a role in SNARE assembly at the ER (By similarity) | MASFVTEVLAHSGSLEKEDLGTRISRLTRRVEEIKGEVCNMISKKYSEFLPTMQSAQALVTQVDTLSNDIDQLKSRIETEVCRDLHISTVEFTNLKQRLERDSVVLNLLKQLQEFSSAIEEYNSALAEKKYIPAARLLEEAQECLKLLKSKKCFDLKMLKSLSMELTVQKQNILYHLGEDWQKLVVWKFPPSKDTSSLESCLQTELHLCTEQPEKEMTPLPSISSVLLAFSILGELPTKLKSFGQMLLKYILKPLVTCPSLHAVIERQPNSVSICFQSLATDSEHPPPPEAFAKIQLVLEVLQKQLLDLPLDADLEIGKVPEIVLAEMLGEVIWEDLSDCLIRNCLVYSIPTNSSKLQQYEEIIQSTEEFEKSLKEMRFLKGDTTDLLKYARNINSHFANKKCQDVIVAARHLMTSEIHNTVKIGPDCEETLPDLPSPDADHRLQVQVCKVQFTDAGNLEPETSLDPRSFSLPTCRISEAVKKLMELAYQTLLEATTSSDQCAVQLFYSVRNIFHLFHDVVPTYHKENLQKLPQLAAIHHNNCMYIAHHLLTLGHQFRSRLTPILCDGTTTFVDLVPGFRRLGTECFLAQMRTQKGELLERLSSARSFANMDDEENYSAASKAVRQVLHQLKRLGIVWQDVLPVNIYCKAMGTLLNTVIAEMIGRITALEDISTEDGDRLYSLCKTVMDEGPQVFAPLSDENKNKKYQEEVPVYVSKWMPFKELMIMLQASLQEIGDRWADGKGPLATAFPSSEVKALIRALFQNTERRAAALAKIK |
Q9SLV1 | [
0.023964913561940193,
-0.05962684750556946,
-0.08120737969875336,
-0.06903217732906342,
-0.045789919793605804,
-0.17291530966758728,
0.03284381330013275,
0.17280156910419464,
0.08755001425743103,
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0.06053899973630905,
0.06319922208786011,
0.019877232611179352,
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0.04485679417848587,
0.0724240094423294,
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0.02542118728160858,
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0.028360119089484215,
0.054508425295352936,
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0.11870598793029785,
0.1275971531867981,
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0.0954398587346077,
0.06752978265285492,
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0.06204874441027641,
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0.15359321236610413,
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0.05103299766778946,
0.017749838531017303,
0.013910248875617981,
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0.022341499105095863,
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0.09898773580789566,
0.023058559745550156,
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0.03647803142666817,
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0.1601702719926834,
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0.03224774822592735,
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0.003924286924302578,
0.01639845222234726,
0.013259895145893097,
-0.18696874380111694,
0.07563918828964233,
0.07783516496419907,
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0.02345777489244938,
0.2171221226453781,
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0.08897634595632553,
0.002315363148227334,
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0.004386998247355223,
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0.027269266545772552,
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-0.027655603364109993,
0.11052226275205612,
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0.03915141895413399,
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-0.11155322194099426,
-0.09326042979955673,
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0.04580897465348244,
0.059520430862903595,
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0.14264874160289764,
0.0781487450003624,
0.05880126729607582,
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0.04224671050906181,
0.049040913581848145,
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-0.049335017800331116,
-0.0784001499414444,
0.10559295862913132,
0.026769153773784637,
0.05156184360384941,
-0.03669198602437973,
-0.18997164070606232,
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0.1396520733833313,
-0.029753319919109344,
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-0.06844725459814072,
-0.06876206398010254,
-0.07604426145553589,
-0.10170280933380127,
0.07374435663223267,
0.11358097195625305,
-0.08544213324785233,
-0.07349575310945511,
-0.08550643175840378,
0.21089370548725128,
0.0032789951656013727,
0.03211616352200508,
-0.0955316498875618,
0.034076791256666183,
0.01862211711704731,
0.06829522550106049
] | Protein ZW2 | Arabidopsis thaliana | Magnoliopsida | Streptophyta | ZW2 | 225 | 2 | 1 | 3,702 | 3,702 | May be involved in the regulation of abscisic acid (ABA) sensitivity | MPITSSSETFASFFNDWLCRHRQFVQQLAHLADETTIVTPIEEESLVSNFLSHYLQYYEEKSVAMSVAGDDIYDFFSPPWLSSYEKLILWIGGFKPGMVFKLITTSVNDLTSHQIDQLESIRLETKRRERDLMRRFALLQQSVGDPLLMVPFRRIGVLRLGEGEQPEMEDAMEVLKVEMIKAMKNADQLRCVTVGKVVEVLNPRQSIKLLRAAGEFYLRLRDLGV |
A6QM04 | [
0.006145646329969168,
-0.08964955806732178,
-0.08430412411689758,
-0.03837558999657631,
-0.10646224766969681,
-0.19927439093589783,
0.02952500618994236,
0.08406976610422134,
0.027568945661187172,
0.11536143720149994,
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0.025640975683927536,
0.012747126631438732,
0.030180325731635094,
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0.008256911300122738,
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0.06941500306129456,
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0.08049013465642929,
0.06533212959766388,
0.0032959328964352608,
0.14993934333324432,
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0.05827441066503525,
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0.014786351472139359,
0.032566629350185394,
0.11212388426065445,
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0.08586112409830093,
0.06050676852464676,
0.03612561523914337,
0.02946729212999344,
0.026338713243603706,
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0.0013058432377874851,
0.0801054984331131,
0.03219257667660713,
0.060765475034713745,
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0.15349353849887848,
0.04670840501785278,
0.06545667350292206,
0.030817216262221336,
0.02168991044163704,
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0.019232695922255516,
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0.051118556410074234,
0.07875606417655945,
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0.20807866752147675,
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0.03745090961456299,
0.09772545099258423,
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0.013243164867162704,
0.055055078119039536,
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0.007913792505860329,
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-0.011362939141690731,
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0.11451220512390137,
0.07494334876537323,
-0.05878292769193649,
-0.19686777889728546,
-0.02694077417254448,
0.09679441899061203,
0.1603352129459381,
0.05749855190515518,
-0.06011120602488518,
0.19180738925933838,
0.13169607520103455,
-0.05696016550064087,
-0.028772830963134766,
-0.008401064202189445,
0.05399153009057045,
0.017925983294844627,
0.1305140256881714,
0.011174836196005344,
-0.04836852476000786,
-0.16372069716453552,
0.08741484582424164,
-0.018194857984781265,
0.03229089826345444,
-0.1408059000968933,
0.0637148767709732,
-0.013314144685864449,
-0.04150110483169556,
0.021346569061279297,
-0.0652356743812561,
0.04832877218723297,
-0.021352220326662064,
-0.14078564941883087,
0.1296016424894333,
0.10288491100072861,
0.11455749720335007,
-0.07016684114933014,
-0.04948969557881355,
-0.03631795942783356,
0.041106872260570526
] | Protein zwilch homolog | Bos taurus | Mammalia | Chordata | ZWILCH | 589 | 2 | 1 | 9,913 | 9,913 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex (By similarity) | MWSGANRAAEEFYAGLLQEFDENKKGIRKDPFIYEADIQVQLISKGQPNPLKNILHENETIFIVEKVPLEKEEPSPIEELQSEDTAISDLSTGENVGLLALPIGRARQLIGFYTMAHNPNMTHLKINRPVTALPPLWVRCDGSDPEGISWLGAELISTSSNITGIVLYMVTCKVDKNYSVNLEDLKKSHKKRHHLSTLTASGFARYELFKSTALDDTVAASQTTITLDISWSPVDEILQTPPLSSTATLNIKVESGEPRGPLSQLHRELKFLLVLADGLRTGVTEWPEPLEAKSAVELVQEFLNELSKLNEFGDSTKKDTEIVKHDAAAVDGSIECLLTVRGDLDFAEQLWCKMSSSVISYQDLVKCFSLVIQSLQRGAIQPWLHSGSNSLLSKLIHQSYYGTMDTVSLSGTVPVQMLLEIGLDKLKKDYICFFIGQELASLNHLEYFISPSVDTQEQVHRVQKLHHILEIVVSCMLFIKPQHELLFSLTQSCIKYYEQNPLDEQHIFQLPVRPTAVKDLYQNEKPQKWRVEINSGQKKVKTVWQLSDSPPIDHLNFHRPDFSELTLSGSLEERISFTNMVTCSQVHFK |
P0C664 | [
0.11973822116851807,
-0.08681563287973404,
0.0027773273177444935,
0.048472754657268524,
-0.05291719734668732,
-0.06470423936843872,
0.12462049722671509,
0.0695534199476242,
0.1275528073310852,
0.15681134164333344,
0.045258376747369766,
-0.02284812182188034,
-0.03797418251633644,
-0.046588726341724396,
-0.10913627594709396,
-0.10744790732860565,
0.12147478759288788,
0.037855345755815506,
-0.13998886942863464,
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-0.06990234553813934,
-0.13347391784191132,
0.04339887574315071,
-0.05054323747754097,
0.0017826127586886287,
0.12624166905879974,
-0.09770330786705017,
0.047266922891139984,
0.16560496389865875,
-0.018870307132601738,
0.06460194289684296,
-0.004369031637907028,
-0.12833380699157715,
-0.040950074791908264,
0.06293974071741104,
-0.10531030595302582,
0.03323105350136757,
-0.029727105051279068,
0.12020937353372574,
0.0690896287560463,
-0.05837978795170784,
-0.1102265939116478,
-0.01238226518034935,
-0.013789411634206772,
0.029561277478933334,
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-0.06866447627544403,
0.054003674536943436,
-0.1569594442844391,
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-0.09031391888856888,
0.08019134402275085,
-0.08160463720560074,
-0.028691858053207397,
-0.005019448231905699,
-0.003281294135376811,
0.025416530668735504,
0.10595632344484329,
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0.04259057343006134,
-0.05131937935948372,
-0.026653455570340157,
-0.13398760557174683,
-0.06992938369512558,
-0.22069157660007477,
0.12141630053520203,
0.11975463479757309,
-0.04248029738664627,
-0.0627983808517456,
0.2518159747123718,
-0.11935784667730331,
-0.1312570720911026,
0.020204337313771248,
0.06187749281525612,
-0.06287219375371933,
0.003914074040949345,
-0.02111262083053589,
-0.031217167153954506,
-0.057846516370773315,
-0.11468403786420822,
-0.060737330466508865,
-0.03893990069627762,
0.008868755772709846,
-0.029054513201117516,
-0.14622290432453156,
-0.13897883892059326,
0.0395941361784935,
0.1795804351568222,
-0.019931752234697342,
0.02308983914554119,
-0.006786441430449486,
-0.1477736532688141,
-0.10001116991043091,
0.053986769169569016,
0.09144747257232666,
0.09209073334932327,
0.013549602590501308,
0.05076582729816437,
0.04572466015815735,
-0.10448678582906723,
-0.10461856424808502,
0.08586367964744568,
0.07499411702156067,
0.03212545067071915,
0.059018608182668686,
0.05285719037055969,
-0.040609799325466156,
-0.051525525748729706,
0.15469130873680115,
0.009737316519021988,
-0.06250125169754028,
-0.10357844829559326,
0.15525513887405396,
-0.08757945150136948,
-0.13650061190128326,
-0.05608527362346649,
0.07921747118234634,
-0.05339328572154045,
-0.06795517355203629,
-0.11055608838796616,
0.09231556951999664,
0.18017637729644775,
0.05854196473956108,
-0.0846785232424736,
-0.08102352172136307,
-0.015862824395298958,
0.05339653789997101
] | Protein zwilch homolog | Caenorhabditis briggsae | Chromadorea | Nematoda | zwl-1 | 639 | 3 | 1 | 6,238 | 6,238 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for chromosome segregation, the assembly of the dynein-dynactin and mdf-1-mdf-2 complexes onto kinetochores and spindle pole separation. Its function related to the spindle assembly machinery and kinetochore-microtubule attachments likely depends on its association in the mitotic RZZ complex. The RZZ complex recruits the spindly-like protein spdl-1 to kinetochores. To prevent irregular chromosome segregation, the complex also inhibits the attachment of the kinetochore-associated NDC80 complex to microtubules. The recruitment of spdl-1 to kinetochores relieves this inhibition. Required for embryonic development | MSIKLEDLHSFNEAVLFKGEEDEAPAPVLLLDKYRVRLVPITELPLVSNYSNTSQLGLNSEEVLVIDSPIESAEKQKTSSLLNRRENKKTIKSEKEDESMDMETAEGDKENTVSETGGGPLVTSFLTLDKLEKDGVNDVEIVGLDCEIQFFDANPIPFEDGISLQRFLRLESSKNFSAAVDKLPIWISTIGHHFPSVCWLAAGRTNKNVQVSGATRILGYFNENSQKLVKQLNEACGAAQVNRYRAVYDVIRKIATPTREAPGEVIIDMRWNTKSSLVLLEQPDNAADCTIKIDLGWGDNRFFIDETIFEQLFFVLNLADVLANPEKEVVFRSESDKFDDLVQEMKQLVEACSHEDNVFASNEKSEQVTDKVWNIVRKCSDVKQATMLFKNFLQALTYGKIKSHVQEGNKSHLASLIRASKTCDFRMPILERLSTIEMMMEIGVESLRGRIINKFSDTLQFPSDELTFILKTCENDLSTLEGTLHSSVVSLLPITMAMATIHQIFGFLNVKDLVVLPDLARRVLTKYTTGMVEKAKRGETETDYVFETTLPLLRMNKEAFMHKRPRIWTCENTNTVGANVQTRAMTTLELEPSLEHVCRLVNASRPVRPIDEDNRKPTEEERNADYTVSHTIFSYLPKL |
Q95XP9 | [
0.060089658945798874,
-0.055596545338630676,
-0.0386044979095459,
-0.06849419325590134,
-0.06428857892751694,
-0.12534017860889435,
0.0573573000729084,
0.1313670575618744,
0.12529778480529785,
0.11485493928194046,
-0.03612201288342476,
0.017033308744430542,
-0.022548146545886993,
-0.09516695141792297,
0.01740480214357376,
0.029322708025574684,
0.07875144481658936,
0.12187188118696213,
-0.16233722865581512,
-0.09653738886117935,
-0.03281643986701965,
-0.06488078832626343,
-0.002814380917698145,
0.056032948195934296,
0.008388585411012173,
0.06647796183824539,
-0.14338122308254242,
0.013318332843482494,
0.08806124329566956,
-0.0529770664870739,
0.0911366418004036,
0.01774526946246624,
-0.06516101956367493,
-0.03471972793340683,
0.039672814309597015,
-0.07745136320590973,
0.026925139129161835,
0.03502677381038666,
0.14749567210674286,
0.07619176805019379,
-0.11404456943273544,
-0.14775799214839935,
0.01247464120388031,
0.055322613567113876,
0.06614208221435547,
0.0040800729766488075,
0.0238320454955101,
0.03306236490607262,
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0.2028544545173645,
0.026031149551272392,
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0.01461103931069374,
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0.08663178235292435,
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0.11209555715322495,
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-0.015259609557688236,
0.10178538411855698
] | Protein zwilch homolog | Caenorhabditis elegans | Chromadorea | Nematoda | zwl-1 | 630 | 1 | 1 | 6,239 | 6,239 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis (PubMed:18765790). Required for chromosome segregation, the assembly of the dynein-dynactin and mdf-1-mdf-2 complexes onto kinetochores and spindle pole separation (PubMed:18765790). Its function related to the spindle assembly machinery and kinetochore-microtubule attachments likely depends on its association in the mitotic RZZ complex (PubMed:18765790). The RZZ complex recruits the spindly-like protein spdl-1 to kinetochores (PubMed:18765790). To prevent irregular chromosome segregation, the complex also inhibits the attachment of the kinetochore-associated NDC80 complex to microtubules (PubMed:24231804). The recruitment of spdl-1 to kinetochores relieves this inhibition (PubMed:24231804). Required for embryonic development (PubMed:18765790, PubMed:19109417) | MPLTIEQLKQYNEKMAAKGEEDDAPAPVLLLDKYRVRVLPLTSIPFVMNHSSVSQLSLSSEDVLVVDFPSKGTGSGAGKAEKKMIFKKKIEPMEDSFEDKENVNEGGPLMTSFLTLEKLRKGMVGDVEIIGYECETSFFDANPIPLSDGVSLQRYIRLNCSEHFSPSISTLPVWISTTSSKFPSICWLAAGRTNRNVQFAAATRVLGHFNNENSERVVKQLNQACGTSQLNKYRAVYEEIRKIATENRPAPGEVTIDVRWSTKSTLVLLEHPDNAADCTIKIDLGWGDKRFFVDDEIFEQLFFVLNLADVLANPDNEVIFPMAPPANFDDLVQEMDALVEASSREDNVFVSNENFRGGDITDKVWNIVRKCNDVKQVTLLFRNFLQALAYGKIKSHAQERNKSHLASLIRISKSSEFKIPVLERLSTIDMMMEIGVESLRRRVIDIFSSQLLYPSDELEFILQTCENDLPAGNGAMNSAAISLLPITMALATANRIYELLNEKDHVILPDLTRRILQKYTASMIEKSRRGETETEYTFETTLPLLRMYKEGFMSKRPCIWTCENSNTVGANVQARVLTSLELQPSLEHINRLVNDSRPVWTATEEKPAMIKDLNADYTVVHTIFSYLPKM |
A5WWB6 | [
0.10860320925712585,
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0.024417182430624962,
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-0.08006706833839417,
0.0006298863445408642
] | Protein zwilch homolog | Danio rerio | Actinopteri | Chordata | zwilch | 583 | 2 | 1 | 7,955 | 7,955 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and mad1-mad2 complexes onto kinetochores (By similarity) | MGSKIVSDANAFVKFLKLCQDESKDNCTYMDDVSVLLVKKEQLLHDIIGEKNQPIFICEKAQTKYEPEATETSADTSDVEDVLFKVEQDPGPQPLSIMKARQLLSWYTMAHNPNMSRLKAPENLHPLWVRCDKSDPCATAWLGVEITYSGNKTSGVKLYTVCCKGPTGDETAFTTLDELKQEHQNRHHTSAVSTKGYAQYNLFCSLTEESLMFESQSSVIASLTWNHVEKMLECPPLSSKATLNIKVAVGDIRSPLYQTYREMEFLLALAGGLRTGEIEWLEPVETQSAVDLTRALIEELENLAHGVPGHSAKASEKQKAKPDAAFSSMVIERGDLDFTEQLWEKMRKSVTSYQDITECMKIVVKAVKLGKIKPWIHKDSNSTLSKLILQSYQQQIDSVPLTGLAPANMLLELGLDKIRKDFINYLVGKELTTLNYLSYYLDTEVDLQEQVVRVRKLHHLLEILGTCSTFLSLPHERLFLFTQSCLQYYKTSNYDEDHIFQLQIKPALISYFYEKEQPFSWAVEVSSGQGSKEVKTSLYLSDKPLVDHIHLDLDVSLNESVNGDSEKMFYYRTMVSCSLINFI |
Q9VA00 | [
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0.13091278076171875,
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0.0775437280535698,
0.07725919783115387,
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0.01211810577660799,
0.08619462698698044,
0.059523701667785645,
0.0752197653055191,
0.01641588658094406,
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0.08047361671924591,
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0.05248391255736351,
0.07975723594427109,
0.02929571270942688,
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0.09950762987136841,
0.10805372148752213,
0.04547164961695671,
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0.02398357354104519,
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0.029345430433750153
] | Protein zwilch | Drosophila melanogaster | Insecta | Arthropoda | Zwilch | 641 | 1 | 1 | 7,227 | 7,227 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis (PubMed:15886105, PubMed:17576797). Required for the assembly of the dynein-dynactin, Mad2 complexes and spindly/CG15415 onto kinetochores (PubMed:15886105, PubMed:17576797). Its function related to the spindle assembly machinery is proposed to depend on its association in the RZZ complex (PubMed:22685323). Failure to assemble the complex due to the absence of any one of its components, results in the incorrect redistribution of the remaining components to diverse membrane compartments (PubMed:22685323) | MSASANLANVYAELMRRCGESYTITYGAPPTYLVSMVGAAEAGKKIVLVFKEDRNGAVARLRTTPTRAAPKKEGSADLDLTGSPLKDDCLVDAIADLSIDLQLDHSNPWKLEEEYQRGIPVDKARSIVCSEFLQLAEGLGSVWFLCDGSDLGQTQLLQYEFNPTHFSRGILSYQGVRPAYLVTSQALVRHHGKTPDETLIENSYQVNPHMRLRCSWTSSAALPLLVNLNDCDVALNHTFRVGDCGPLTQDFMNQLRILVYIREDIVSYHTDVKQGVSRDPTYRCGSGIDMDELRESINQTMTDVSGLIGRYSISNAEFDIEDVVQRAKVRQLTDLTDKLWELLKCCHSYKDLKIAFSMLFQCAARCNIVNTPTNKNRLAKIITELANRRLAMPCLSGAEPLELLLEIGLEKLYKDYEFIYTESKMCSTNLLKDDSSGASMDDGSPQNLPQLRKSLHNAVRGDPTPGAGMRKTLLHHHGAVNSRSTKYAGSDDDAGFKNSHFDEHESTERISKLFQIHCTLEHLLMMHIHLNLANVYNDVCSELLKKPPKLVESIDDQLSDVMDIRLSAHYVRDHLDGKDPYSRHITMRSHNKFRELKTTFYFNSENICPPNLAQCFQCDDKEMVKERTYHSWIYHKIRSLK |
Q9H900 | [
0.03415137529373169,
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-0.054646123200654984,
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0.055437687784433365,
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0.06696923822164536,
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0.18458418548107147,
0.11936438083648682,
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0.05986850708723068,
0.03372367471456528,
0.10221715271472931,
0.004188216757029295,
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0.12435342371463776,
0.01130928099155426,
0.013882354833185673,
-0.1290954202413559,
0.10278603434562683,
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0.015454980544745922,
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0.07319197058677673,
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-0.13762377202510834,
0.15737149119377136,
0.09466121345758438,
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-0.08204621821641922,
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-0.03518027439713478,
-0.007078881375491619
] | Protein zwilch homolog | Homo sapiens | Mammalia | Chordata | ZWILCH | 591 | 1 | 2 | 9,606 | 9,606 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex (PubMed:15824131) | MWERLNCAAEDFYSRLLQKFNEEKKGIRKDPFLYEADVQVQLISKGQPNPLKNILNENDIVFIVEKVPLEKEETSHIEELQSEETAISDFSTGENVGPLALPVGKARQLIGLYTMAHNPNMTHLKINLPVTALPPLWVRCDSSDPEGTCWLGAELITTNNSITGIVLYVVSCKADKNYSVNLENLKNLHKKRHHLSTVTSKGFAQYELFKSSALDDTITASQTAIALDISWSPVDEILQIPPLSSTATLNIKVESGEPRGPLNHLYRELKFLLVLADGLRTGVTEWLEPLEAKSAVELVQEFLNDLNKLDGFGDSTKKDTEVETLKHDTAAVDRSVKRLFKVRSDLDFAEQLWCKMSSSVISYQDLVKCFTLIIQSLQRGDIQPWLHSGSNSLLSKLIHQSYHGTMDTVSLSGTIPVQMLLEIGLDKLKKDYISFFIGQELASLNHLEYFIAPSVDIQEQVYRVQKLHHILEILVSCMPFIKSQHELLFSLTQICIKYYKQNPLDEQHIFQLPVRPTAVKNLYQSEKPQKWRVEIYSGQKKIKTVWQLSDSSPIDHLNFHKPDFSELTLNGSLEERIFFTNMVTCSQVHFK |
Q8R060 | [
0.0400843620300293,
-0.06404862552881241,
-0.07860950380563736,
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0.06461083143949509,
0.02369423769414425,
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-0.0035759946331381798,
-0.06717513501644135,
-0.011050735600292683
] | Protein zwilch homolog | Mus musculus | Mammalia | Chordata | Zwilch | 589 | 1 | 1 | 10,090 | 10,090 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex (By similarity) | MWSRMNRAAEEFYARLRQEFNEEKKGASKDPFIYEADVQVQLISKGQPSLLKTILNENDSVFLVEKVVLEKEETSQVEELQSEETAISDLSAGENIRPLALPVGRARQLIGLYTMAHNPNMTHLKIKQPVTALPPLWVRCDGSDPEGTCWLGAELITTNDIIAGVILYVLTCKADKNYSEDLENLKTSHKKRHHVSAVTARGFAQYELFKSDDLDDTVAPSQTTVTLDLSWSPVDEMLQTPPLSSTAALNIRVQSGESRGCLSHLHRELKFLLVLADGIRTGVTEWLEPLETKSALEFVQEFLNDLNKLDEFDDSTKKDKQKEAVNHDAAAVVRSMLLTVRGDLDFAEQLWCRMSSSVVSYQDLVKCFTLILQSLQRGDIQPWLHSGSNSLLSKLIHQSYHGAMDSVPLSGTTPLQMLLEIGLDKLKKDYISFFVSQELASLNHLEYFISPSVSTQEQVCRVQKLHHILEILVICMLFIKPQHELLFSLTQSCIKYYKQNPLDEQHIFQLPVRPAAVKNLYQSEKPQKWRVELSNSQKRVKTVWQLSDSSPVDHSSFHRPEFPELTLNGSLEERTAFVNMLTCSQVHFK |
Q5RA78 | [
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0.12314759939908981,
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-0.03529737517237663,
-0.0071655516512691975
] | Protein zwilch homolog | Pongo abelii | Mammalia | Chordata | ZWILCH | 591 | 2 | 1 | 9,601 | 9,601 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and MAD1-MAD2 complexes onto kinetochores. Its function related to the spindle assembly machinery is proposed to depend on its association in the mitotic RZZ complex (By similarity) | MWERLNCAAEDFYSRLLQKFNEEKKGIRKDPFLYEADVQVQLISKGQPNPLKNILNENDIVFIVEKVPLEKEETSHIEELQSEETAISDFSTGENVGPLALPVGKARQLIGLYTMAHNPNMTHLKINLPVTALPPLWVRCDSSDPEGTCWLGAELITTNNSITGIVLYVVSCKADKNYSVNLENLKNLHKKRHHLSTVTSKGFAQYELFKSSALDDTITASQTAIALDISWSPADEILQIPPLSSTATLNIKVESGEPRGPLNHLYRELKFLLVLADGLRTGVTEWLEPLEAKSAVELVQEFLNDLNKLDGFGDSTKKDTEVETLKHDTAAVDRSVKRLFKVRSDLDFAEQLWCKMSSSVISYQDLVKCFTLIIQSLQRGDIQPWLHSGSNSLLSKLIHQSYHGTMDTVSLSGTIPVQMLLEIGLDKLKKDYISFFIGQELASLNHLEYFIAPSVDIQEQVYRVQKLHHILEILVSCMPFIKSQHELLFSLTQICIKYYKQNPLDEQHIFQLPVRPTAVKNLYQSEKPQKWRVEIYSGQKKIKTVWQLSDSSPIDHLNFHKPDFSELTLNGSLEERIFFTNMVTCSQVHFK |
Q6IRM9 | [
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0.032883916050195694,
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0.04284758120775223,
0.0597219355404377,
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0.12983736395835876,
0.11115003377199173,
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0.018245581537485123,
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] | Protein zwilch homolog | Xenopus laevis | Amphibia | Chordata | zwilch | 597 | 2 | 1 | 8,355 | 8,355 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and mad1-mad2 complexes onto kinetochores (By similarity) | MWAERHRAAVELQQFLSSVYEQVKKEESLGPFQFKDDIQVHVVCDGHCKPLESFCSGSEVLYILEKKPLTLEDNVLDETENNEGISFYTSLQEIPQPQAIPTMRARQFLTSYTLTHNPNMVQLNSGAPVKVLPPLWVRCDCSDAEGTCWLGAEPIKSSRNEITGMSFRTVTCAGPTADKSTFPSLDSLRQAHKERHYSSVMQTRGFAQYDLFGCNTVENSVIESQSSVTVDFVWNGVERILQLPPLASAATLNIKVESGDLRSPVYSVYKELDFLLVLAEGLKTGVTEWPETGETKSAVDLVQLLLNDLKNKVDGLTSSVSKKDNEKIKSDTAAVDCSIQSFITERGDLDFAEMLWCRMRKSVSSYQDVVNCFSLVIQSLKNGEVHPWIHRGSSSALSKLIQQSYHGKMQSVSLTGLTPMRMLLEIGLDKMKKDYISCFIGQDLATFNYLDYFISSSVDIQEQVQRVKKLHHMLEVVVVCNAFLSLGHENLFPLTQSCLKYYKENPWNEQHVFQLPIRPSVISTFYQNSHPQTWRVEIISGHGQKEVKTTWQLTSRRPVDHVSFAVPDVPIDMTISGENEEIVYYPTQVSCSQVNFC |
Q0IJ01 | [
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0.14915858209133148,
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0.08865732699632645,
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0.03478047996759415,
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0.07564260810613632,
-0.15685546398162842,
0.11616633087396622,
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0.13713715970516205,
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0.014949378557503223,
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] | Protein zwilch homolog | Xenopus tropicalis | Amphibia | Chordata | zwilch | 597 | 2 | 1 | 8,364 | 8,364 | Essential component of the mitotic checkpoint, which prevents cells from prematurely exiting mitosis. Required for the assembly of the dynein-dynactin and mad1-mad2 complexes onto kinetochores (By similarity) | MWAERHRAAVELQQFLSSIYEQVKKGESLGPFQYKDDVQVHVVCDGHCKPLENFCSGSEVLYIMEKKPLTLEDNALDETENNEGISFYMSLQESPQPQAIPTMSARQFLTSYTLTHNPNMIQLNSGVPVKVLPPLWVRCDSSDAEGTCWLGAEPIKSNRNEITGMSFRTVTCAGPTADKSTFPSLDSLRQAHKERHYSSAMQTRGFAQYDLFGSNTVENSVIESQSSVTVDFVWNGVERILQLPPLTSAATLNIKVESGDLRSPVYSVYKELDFLLVLAEGLKTGVTEWPETSETKSAVDLVQHLLNDLKNKVDGLSTSVSKKDNEKIKSDTAAVDCSIQSFITERGDLDFAEMLWCKMRKSVSSYQDVVNCFSLVIQSLKHGEMHPWIHRGSSSTLSKLIQESYHGDMQSLSLTGLTPMRMLLEIGLDKMKKDYINCFIGQDLATFNYLDYFICTSVDLQEQVQRVKKLHHMLEVVVVCNAFLSLGHENLFPLTQSCLKYYKENPWNEQHVFQLPIRPSVISTFYQNSHPQTWRVEIISGHGQKEVKTTWQLTSRRPVDHVSFAVPDVPIDMTISGDNEELVYYPTQVSCSQVHFC |
Q2TBH8 | [
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0.06625045090913773,
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] | ZW10 interactor | Bos taurus | Mammalia | Chordata | ZWINT | 286 | 2 | 1 | 9,913 | 9,913 | Part of the MIS12 complex, which is required for kinetochore formation and spindle checkpoint activity. Required to target ZW10 to the kinetochore at prometaphase (By similarity) | MGAAESEVETAAREVLAKVADIQEPVGFQEEAELPAQILAEFVMDSRKKDKLLCSQLQVVDFLQNFLVQEGTAQDQNPLASEDTSRQKALEAKEQWKELKATYQEHVEVITNSLTEALPKVEEAQIKQAQLQEALKQLQAKKQMAMEKLRIAQKQWQLEQEKHLQNLAEASSEVRERQTGAQQELQRLYQELGTLKQQAGQEKDKLQRHQTFLQLLYTLQGKQLFNEAEAEIPQELDLPKDKLQQVTQPQEQNTQDTMGREADNPQPVGDAGLPWLPGRQQHKEES |
O95229 | [
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] | ZW10 interactor | Homo sapiens | Mammalia | Chordata | ZWINT | 277 | 1 | 2 | 9,606 | 9,606 | Part of the MIS12 complex, which is required for kinetochore formation and spindle checkpoint activity. Required to target ZW10 to the kinetochore at prometaphase | MEAAETEAEAAALEVLAEVAGILEPVGLQEEAELPAKILVEFVVDSQKKDKLLCSQLQVADFLQNILAQEDTAKGLDPLASEDTSRQKAIAAKEQWKELKATYREHVEAIKIGLTKALTQMEEAQRKRTQLREAFEQLQAKKQMAMEKRRAVQNQWQLQQEKHLQHLAEVSAEVRERKTGTQQELDRVFQKLGNLKQQAEQERDKLQRYQTFLQLLYTLQGKLLFPEAEAEAENLPDDKPQQPTRPQEQSTGDTMGRDPGVSFKAVGLQPAGDVNLP |
Q9CQU5 | [
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0.1564876139163971,
0.046571988612413406,
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-0.14828401803970337
] | ZW10 interactor | Mus musculus | Mammalia | Chordata | Zwint | 252 | 1 | 1 | 10,090 | 10,090 | Part of the MIS12 complex, which is required for kinetochore formation and spindle checkpoint activity. Required to target ZW10 to the kinetochore at prometaphase (By similarity) | MADAEKNAVAEKNNAVATKEVLAEAAAILEPVGLQEEAELPAKIMEEFMRNSRKKDKLLCSQLQVVNFLQTFLAQEDTEQSPDALASEDASRQKATETKEQWKDMKATYMDHVDVIKCALSEALPQVKEAHRKYTELQKAFEQLEAKKRVLEEKLQLAQKQWVLQQKRLQNLTKISAEVKRRRKRALEKLDGSHQELETLKQQAGQEQEKLQRNQSYLQLLCSLQNKLVISEGKAEDKDVKGRALTAKSKSP |
Q8VIL3 | [
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0.09419519454240799,
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0.054556652903556824,
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0.058601126074790955,
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0.072904571890831,
0.05673057958483696,
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0.0312984324991703,
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-0.16834625601768494
] | ZW10 interactor | Rattus norvegicus | Mammalia | Chordata | Zwint | 266 | 1 | 1 | 10,116 | 10,116 | Part of the MIS12 complex, which is required for kinetochore formation and spindle checkpoint activity. Required to target ZW10 to the kinetochore at prometaphase (By similarity) | MADAEKNAVAEKNAVAEENAVAEENAVADKNATKEVLAEAASVLEPVGLPEEAELPAKIMEEFMRNSRKKDKLLCSQLQVVNFLQTFLAQEDNTDQNPDALASEDTSRQKATETKEQWKELKATYMDHVDVIKCALSEALPQVKEAHRKYTELQKAFEQLEAKKRVLEEKLQLAQKQWVLQQKRLQNLTKISAEVKRRRKRALEKLDGSHQELETLKQQAGQEQEKLQRNQSYLQLLCSLQNKLVISESKADDKDVKGPALPPKSP |
Q9SVY1 | [
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0.07375388592481613,
0.01690215803682804,
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] | Zinc finger protein WIP2 | Arabidopsis thaliana | Magnoliopsida | Streptophyta | WIP2 | 383 | 1 | 1 | 3,702 | 3,702 | Transcriptional regulator required for normal differentiation of the ovary transmitting tract cells and pollen tube growth. In Arabidopsis, the transmitting tract facilitates the transport of pollen tubes to the ovules for fertilization (PubMed:17600712). May play a role in the regulation of AGL8/FUL, which is required for normal pattern of cell division, expansion and differentiation during morphogenesis of the silique (PubMed:23515580). Plays a role in replum development by the activation of the homeobox protein KNAT1 (PubMed:25039392) | MTDPYSNFFTDWFKSNPFHHYPNSSTNPSPHPLPPVTPPSSFFFFPQSGDLRRPPPPPTPPPSPPLREALPLLSLSPANKQQDHHHNHDHLIQEPPSTSMDVDYDHHHQDDHHNLDDDDHDVTVALHIGLPSPSAQEMASLLMMSSSSSSSRTTHHHEDMNHKKDLDHEYSHGAVGGGEDDDEDSVGGDGGCRISRLNKGQYWIPTPSQILIGPTQFSCPVCFKTFNRYNNMQMHMWGHGSQYRKGPESLRGTQPTGMLRLPCYCCAPGCRNNIDHPRAKPLKDFRTLQTHYKRKHGIKPFMCRKCGKAFAVRGDWRTHEKNCGKLWYCICGSDFKHKRSLKDHIKAFGNGHGAYGIDGFDEEDEPASEVEQLDNDHESMQSK |
Q9SGD1 | [
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] | Zinc finger protein WIP3 | Arabidopsis thaliana | Magnoliopsida | Streptophyta | WIP3 | 337 | 2 | 1 | 3,702 | 3,702 | Probable transcriptional regulator | MNSYETKGLSFESPSFIEWLKPQSSTTSSKSVLYRGKTRDAISRSNHHQSQMNMLERSLFLYQPQEPLNTSIQCLPLLNKLMENNSQASDIKEENKDDVVTLQIGFPKYHRGSSEDGSDITFDHQKKPIKREIIEDGVVMMKKRRKMKFDEEIIDSDVEVCGKRFWIPSPAQIHVGPMQFACSICSKTFNRYNNMQMHMWGHGSEFRKGADSLKGTIQPAAILRLPCYCCAEGCKNNINHPRSKPLKDFRTLQTHYKRKHGSKPFSCGKCGKALAVKGDWRTHEKNCGKLWYCTCGSDFKHKRSLKDHIRSFGSGHSPHPSLLFDGFEEDTECVTTE |
Q8W030 | [
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] | Zinc finger protein WIP4 | Arabidopsis thaliana | Magnoliopsida | Streptophyta | WIP4 | 412 | 2 | 1 | 3,702 | 3,702 | Probable transcriptional regulator | MLFSTVLSHRTLYILTCPNTLIHSYTHPHIHAYLAFTGFLTQLHHLEISCLLLLFFSLSSLLKLMADPDCIFRNGYVDYYNYSFNYATSLSRIYNSHDSFYYPHQTTNPNINENPNLTSPDSPPLREALPLLSLSPIHKHQEPTANHHEYYFMETTETSSNSNFLDQCQDSYRHDVTVDLHLGLPNLGDGGSSSSDVVLDSTDHQEGHHDHHQDQGLEVTMASDHDDEHGGLQRGNHLHHFWIPTPSQILMGPTQFSCPLCFKTFNRYNNMQMHMWGHGSQYRKGPESLRGTQPTAMLKLPCYCCAPGCKNNIDHPRARPLKDFRTLQTHYKRKHGVRPFACRRCGKAFAVKGDWRTHEKNCGKLWYCSCGSDFKHKRSLKDHVKAFGNGHVPCCGIDHEEEEAASDVEQQE |
Q8W031 | [
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] | Zinc finger protein WIP5 | Arabidopsis thaliana | Magnoliopsida | Streptophyta | WIP5 | 337 | 2 | 1 | 3,702 | 3,702 | Probable transcriptional regulator | MSNPACSNLFNNGCDHNSFNYSTSLSYIYNSHGSYYYSNTTNPNYINHTHTTSTSPNSPPLREALPLLSLSPIRHQEQQDQHYFMDTHQISSSNFLDDPLVTVDLHLGLPNYGVGESIRSNIAPDATTDEQDQDHDRGVEVTVESHLDDDDDHHGDLHRGHHYWIPTPSQILIGPTQFTCPLCFKTFNRYNNMQMHMWGHGSQYRKGPESLRGTQPTGMLRLPCFCCAPGCKNNIDHPRAKPLKDFRTLQTHYKRKHGSKPFACRMCGKAFAVKGDWRTHEKNCGKLWYCSCGSDFKHKRSLKDHVKAFGNGHVPCGIDSFGGDHEDYYDAASDIEQ |
Q9FX68 | [
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0.007182885427027941,
0.08532559871673584,
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-0.09983820468187332,
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] | Zinc finger protein WIP6 | Arabidopsis thaliana | Magnoliopsida | Streptophyta | WIP6 | 302 | 2 | 1 | 3,702 | 3,702 | Probable transcriptional regulator (Probable). Involved in leaf vasculature patterning (PubMed:18643975) | MYNNNQYSFSGDEDSVVLSLGPPGQQYPSHNKPTSTKPSSDHEFNHPLTNPNGVTVALHIGPPSSDKETLSGGNNQEGLTARQGQYWIPSLSQILVGPTQFSCSVCNKTFNRFNNMQMHMWGHGSQYRKGPESLRGTKSSSSILRLPCYCCAEGCKNNIDHPRSKPLKDFRTLQTHYKRKHGAKPFRCRKKCEKTFAVRGDWRTHEKNCGKLWFCVCGSDFKHKRSLKDHVRAFGDGHAAHTVSDRVVGIGDADEDDEEEEEEEEDDVEEEDAHEENVRGEKNYGIRYDHFRRYGQISDDNY |
P98168 | [
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] | Zinc finger X-linked protein ZXDA | Homo sapiens | Mammalia | Chordata | ZXDA | 799 | 1 | 2 | 9,606 | 9,606 | Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes | MEIPKLLPARGTLQGGGGGGIPAGGGRVHRGPDSPAGQVPTRRLLLPRGPQDGGPGRRREEASTASRGPGPSLFAPRPHQPSGGGDDFFLVLLDPVGGDVETAGSGQAAGPVLREEAKAGPGLQGDESGANPAGCSAQGPHCLSAVPTPAPISAPGPAAAFAGTVTIHNQDLLLRFENGVLTLATPPPHAWEPGAAPAQQPRCLIAPQAGFPQAAHPGDCPELRSDLLLAEPAEPAPAPAPQEEAEGLAAALGPRGLLGSGPGVVLYLCPEALCGQTFAKKHQLKMHLLTHSSSQGQRPFKCPLGGCGWTFTTSYKLKRHLQSHDKLRPFGCPAEGCGKSFTTVYNLKAHMKGHEQENSFKCEVCEESFPTQAKLGAHQRSHFEPERPYQCAFSGCKKTFITVSALFSHNRAHFREQELFSCSFPGCSKQYDKACRLKIHLRSHTGERPFLCDFDGCGWNFTSMSKLLRHKRKHDDDRRFMCPVEGCGKSFTRAEHLKGHSITHLGTKPFVCPVAGCCARFSARSSLYIHSKKHLQDVDTWKSRCPISSCNKLFTSKHSMKTHMVKRHKVGQDLLAQLEAANSLTPSSELTSQRQNDLSDAEIVSLFSDVPDSTSAALLDTALVNSGILTIDVASVSSTLAGHLPANNNNSVGQAVDPPSLMATSDPPQSLDTSLFFGTAATGFQQSSLNMDEVSSVSVGPLGSLDSLAMKNSSPEPQALTPSSKLTVDTDTLTPSSTLCENSVSELLTPAKAEWSVHPNSDFFGQEGETQFGFPNAAGNHGSQKERNLITVTGSSFLV |
P98169 | [
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] | Zinc finger X-linked protein ZXDB | Homo sapiens | Mammalia | Chordata | ZXDB | 803 | 1 | 2 | 9,606 | 9,606 | Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes | MEIPKLLPARGTLQGGGGGGIPAGGGRVHRGPDSPAGQVPTRRLLLLRGPQDGGPGRRREEASTASRGPGPSLLAPRTDQPSGGGGGGGDDFFLVLLDPVGGDVETAGSGQAAGPVLREEAEEGPGLQGGESGANPAGPTALGPRCLSAVPTPAPISAPGPAAAFAGTVTIHNQDLLLRFENGVLTLATPPPHAWEPGAAPAQQPGCLIAPQAGFPHAAHPGDCPELPPDLLLAEPAEPAPAPAPEEEAEGPAAALGPRGPLGSGPGVVLYLCPEAQCGQTFAKKHQLKVHLLTHSSSQGQRPFKCPLGGCGWTFTTSYKLKRHLQSHDKLRPFGCPAEGCGKSFTTVYNLKAHMKGHEQENSFKCEVCEESFPTQAKLSAHQRSHFEPERPYQCAFSGCKKTFITVSALFSHNRAHFREQELFSCSFPGCSKQYDKACRLKIHLRSHTGERPFLCDFDGCGWNFTSMSKLLRHKRKHDDDRRFMCPVEGCGKSFTRAEHLKGHSITHLGTKPFVCPVAGCCARFSARSSLYIHSKKHLQDVDTWKSRCPISSCNKLFTSKHSMKTHMVKRHKVGQDLLAQLEAANSLTPSSELTSQRQNDLSDAEIVSLFSDVPDSTSAALLDTALVNSGILTIDVASVSSTLAGHLPANNNNSVGQAVDPPSLMATSDPPQSLDTSLFFGTAATGFQQSSLNMDEVSSVSVGPLGSLDSLAMKNSSPEPQALTPSSKLTVDTDALTPSSTLCENSVSELLTPTKAEWNVHPDSDFFGQEGETQFGFPNAAGNHGSQKETDLITVTGSSFLV |
A2CE44 | [
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] | Zinc finger X-linked protein ZXDB | Mus musculus | Mammalia | Chordata | Zxdb | 873 | 1 | 1 | 10,090 | 10,090 | Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes | MEIPRLLPARGTPQGAGGGGCPAGGGGVHRAPASLACQAPTRRLLLLRGAQDGGPGPRSAEAQRASRGLGPSLNRLAPRPDHRSSGGGRGGGAGGGGGGSGGGGGGGGGGGGGGGGGGSRGGSDDFFLLLLDPVGGDVETVGTEQAGAPVRREEAGAGPRPERRQSAGPPAGRPEPGPRCLSAVPAASPLPAAGPGPAAAAAAAAAAAFAGTITIHNQDLLLRFENGVLTLTTPPLPAWEPGVAPFPQPQPPPQPGALIAPQAAAAGFPPAAAAAAAAAAAGAQLGDCPELPPDLLLAEPAEPAACPAPPEEEAEAPAAAAAQSPRGPAGPGPGPGVVLYLCPEAQCGQTFAKKHQLKVHLLTHSSSQGQRPFKCPLSGCGWTFTTSYKLKRHLQSHDKLRPFGCPVQGCGKSFTTVYNLKAHMKGHEQENSFKCEVCEESFPTQAKLSTHQRSHFEPERPYQCAFSGCKKTFITVSALFSHNRAHFREQELFACSFPGCSKQYDKACRLKIHLRSHTGERPFLCDFDGCGWNFTSMSKLLRHKRKHEDDRRFTCPVEGCGKSFTRAEHLKGHSITHLGTKPFVCPVEGCCARFSARSSLYIHSKKHLQDVGAWKSRCPVPTCNKLFTSKHSMKTHMTKRHNLSQDLLAQLEAANSLTPSSELTSPGQSDLSGAELVSLFSDVPGHGSAAVLDTALVNSGILTIDVASVNSSLAGSLPADNNSNNHSLGQAAEPRALRGAPSDLPQSLDTSLFFGTSVAGYQHSPLDMDDVSAGNVGLFGSLALKNSSLEPQALTPSNKLTVDTEALTPSSTLCENSVSELLTPAKAEWNVHPESDFFGHEEETQFGFSHPTGSHGSQKDTDLITVTGTPFLV |
Q2QGD7 | [
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-0.12125033140182495,
0.06212032213807106,
0.028455400839447975,
0.06869532912969589,
-0.06835303455591202,
-0.09075289964675903,
-0.02180519327521324,
-0.06452873349189758,
-0.08050040900707245,
-0.013995805755257607,
0.18303383886814117,
-0.00817891862243414,
0.01860482431948185,
-0.014610914513468742,
-0.08619064837694168,
-0.010912164114415646,
0.08489637821912766,
0.17023061215877533,
-0.012127156369388103,
-0.07461114227771759,
-0.04276980832219124,
0.12796999514102936,
0.06756338477134705,
0.08527325093746185,
-0.08190102130174637,
-0.09853509813547134,
0.006099454127252102,
-0.0017647652421146631,
-0.055467452853918076,
-0.13524752855300903,
0.06980811059474945,
-0.07162260264158249,
0.03173692896962166,
0.04666434973478317,
-0.11913630366325378,
0.11347096413373947,
0.17896020412445068,
0.012279227375984192,
-0.014339378103613853,
-0.014034419320523739,
0.13172338902950287,
0.11758313328027725,
-0.028898362070322037,
0.14660505950450897,
-0.00552110793069005,
0.1189313679933548,
0.016717910766601562,
0.25406455993652344,
0.014427021145820618,
0.015814095735549927,
0.0026505854912102222,
-0.12909859418869019,
0.09442842751741409,
-0.09637489914894104,
-0.08195365965366364,
-0.025268634781241417,
-0.07046684622764587,
-0.005160277709364891,
0.06583565473556519,
-0.04622218757867813,
-0.11382479965686798,
-0.18069225549697876
] | Zinc finger protein ZXDC | Homo sapiens | Mammalia | Chordata | ZXDC | 858 | 1 | 2 | 9,606 | 9,606 | Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes | MDLPALLPAPTARGGQHGGGPGPLRRAPAPLGASPARRRLLLVRGPEDGGPGARPGEASGPSPPPAEDDSDGDSFLVLLEVPHGGAAAEAAGSQEAEPGSRVNLASRPEQGPSGPAAPPGPGVAPAGAVTISSQDLLVRLDRGVLALSAPPGPATAGAAAPRRAPQASGPSTPGYRCPEPQCALAFAKKHQLKVHLLTHGGGQGRRPFKCPLEGCGWAFTTSYKLKRHLQSHDKLRPFGCPVGGCGKKFTTVYNLKAHMKGHEQESLFKCEVCAERFPTHAKLSSHQRSHFEPERPYKCDFPGCEKTFITVSALFSHNRAHFREQELFSCSFPGCSKQYDKACRLKIHLRSHTGERPFICDSDSCGWTFTSMSKLLRHRRKHDDDRRFTCPVEGCGKSFTRAEHLKGHSITHLGTKPFECPVEGCCARFSARSSLYIHSKKHVQDVGAPKSRCPVSTCNRLFTSKHSMKAHMVRQHSRRQDLLPQLEAPSSLTPSSELSSPGQSELTNMDLAALFSDTPANASGSAGGSDEALNSGILTIDVTSVSSSLGGNLPANNSSLGPMEPLVLVAHSDIPPSLDSPLVLGTAATVLQQGSFSVDDVQTVSAGALGCLVALPMKNLSDDPLALTSNSNLAAHITTPTSSSTPRENASVPELLAPIKVEPDSPSRPGAVGQQEGSHGLPQSTLPSPAEQHGAQDTELSAGTGNFYLESGGSARTDYRAIQLAKEKKQRGAGSNAGASQSTQRKIKEGKMSPPHFHASQNSWLCGSLVVPSGGRPGPAPAAGVQCGAQGVQVQLVQDDPSGEGVLPSARGPATFLPFLTVDLPVYVLQEVLPSSGGPAGPEATQFPGSTINLQDLQ |
Q8C8V1 | [
-0.0777730643749237,
-0.034959156066179276,
-0.0013865395449101925,
-0.03686954453587532,
0.08102478832006454,
0.08118361979722977,
-0.019212694838643074,
-0.060583971440792084,
-0.057192351669073105,
-0.03007110022008419,
0.06557027995586395,
0.018750140443444252,
-0.23136594891548157,
-0.1261996179819107,
0.10765720903873444,
-0.13439147174358368,
-0.07103084027767181,
-0.10427437722682953,
-0.14167998731136322,
0.09276829659938812,
-0.08203994482755661,
-0.019651466980576515,
0.03940398246049881,
-0.030015237629413605,
0.04062239080667496,
-0.034071747213602066,
0.07884378731250763,
0.020113464444875717,
-0.0535956472158432,
0.06461440026760101,
-0.11708956211805344,
0.013752920553088188,
-0.06786295771598816,
0.1667439192533493,
0.11267909407615662,
0.08453695476055145,
-0.075717493891716,
-0.06779160350561142,
-0.018479930236935616,
-0.052530642598867416,
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0.07081586867570877,
0.15256637334823608,
0.07847404479980469,
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-0.1555435061454773,
-0.02536175213754177,
0.15023788809776306,
-0.21703144907951355,
0.08936818689107895,
0.03272385522723198,
-0.01236804947257042,
-0.06516081839799881,
-0.014804147183895111,
0.04764102026820183,
-0.006123731378465891,
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0.0939348042011261,
0.06487314403057098,
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0.03290444612503052,
0.06429524719715118,
-0.06865328550338745,
-0.03817462548613548,
0.043294262140989304,
-0.04345950484275818,
-0.11989052593708038,
0.05460395663976669,
0.01797071099281311,
0.06267047673463821,
-0.054802924394607544,
-0.09091239422559738,
-0.01746959611773491,
-0.05267980694770813,
-0.07596362382173538,
-0.014950410462915897,
0.19025100767612457,
-0.0206635482609272,
0.008689767681062222,
-0.015614856965839863,
-0.08870310336351395,
-0.012800533324480057,
0.08906763792037964,
0.18622717261314392,
-0.025690004229545593,
-0.0735577940940857,
-0.04671784117817879,
0.13623540103435516,
0.07109789550304413,
0.07664473354816437,
-0.08890879899263382,
-0.09974990040063858,
-0.00764094851911068,
0.002647846471518278,
-0.0677894577383995,
-0.12399188429117203,
0.0647483542561531,
-0.07823078334331512,
0.03452187776565552,
0.039905693382024765,
-0.11985660344362259,
0.10778850317001343,
0.16887889802455902,
0.012706355191767216,
-0.012305467389523983,
0.0009308719891123474,
0.13647402822971344,
0.12362132221460342,
-0.022589638829231262,
0.15297721326351166,
0.0069409869611263275,
0.12656837701797485,
0.021066313609480858,
0.26937827467918396,
0.025045815855264664,
0.013698718510568142,
-0.006136746145784855,
-0.11908447742462158,
0.08386928588151932,
-0.09584220498800278,
-0.08115475624799728,
-0.037845369428396225,
-0.06757649034261703,
-0.002014617435634136,
0.07023321092128754,
-0.05558996647596359,
-0.11863098293542862,
-0.18624204397201538
] | Zinc finger protein ZXDC | Mus musculus | Mammalia | Chordata | Zxdc | 858 | 2 | 1 | 10,090 | 10,090 | Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes | MDLPAVLAAPATRGDQHGGGPSRLRRGAGPSLGAGPGRRRLLLLRGPEDGGPGPRPEEAPGPSPPPPEDGGDSFVVLLEVPRAADTHGQEEAEPDSGASPTEQVPAAAPGAALAGTVTIHNQDLLVRFDRGVFTLAAAPAPAAPSLHPATTPGLEPSSAAASRRGPVAASAGSPAYRCPEPQCALSFAKKHQLKVHLLTHGSLQGRRPFKCPLDGCGWAFTTSYKLKRHLQSHDKLRPFSCPVGGCGKKFTTVYNLKAHMKGHEQESLFKCEVCAERFPTHAKLNSHQRSHFEPERPYKCDFPGCEKTFITVSALFSHNRAHFREQELFSCSFPGCNKQYDKACRLKIHLRSHTGERPFICDSDSCGWTFTSMSKLLRHKRKHDDDRRFTCPVEGCGKSFTRAEHLKGHSITHLGTKPFECPVEGCCARFSARSSLYIHSKKHLQDVGTPKSRCPVSSCNRLFTSKHSMKAHVVRQHSRRQDLVPQLEAPSSLTPSSELSSPGQSELTNIDLAALFSDTPANSSSSTAGSDEALNSGILTIDVTSVSSSLGGNLPTNNNSLGPMDPLVLVAHGDMPPSLDSPLVLGTSATVLQPGSFSADDSQAMSTGAVGCLVALPVRNLNQDSPALTPSNNLTAPGTTPTSSDTTQETGSVPDLLVPIKVEQDLSPVPDVVQGQKESHGPSQSVLSSSTERPGAQKDSELSAGTGSLYLESGGSARTDYRAIQLVKKKKQKGTGSDEGASDSAHRKVKGGTINPPHVHSGQHSCFCGTLMVPSGGLTVPAPAAGLQCVQIPVLQDDPSGEGGLPLGLSPQRSAFHPYFTVDLPVYVLQEVLPAPGGFAGLETAQVPGSTINLRDLE |
Q6WRX3 | [
-0.06221406161785126,
-0.14996486902236938,
0.016643214970827103,
-0.08897601068019867,
-0.04586336761713028,
-0.013683704659342766,
-0.0256425179541111,
0.10209965705871582,
0.049363333731889725,
0.16407155990600586,
0.005824686028063297,
-0.02715294435620308,
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0.013531030155718327,
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-0.2723561227321625,
0.04948168247938156,
0.05142458528280258,
0.010018954053521156,
0.15972183644771576,
0.008416236378252506,
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0.13153919577598572,
0.09573591500520706,
0.10302778333425522,
0.06296952813863754,
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0.0273810513317585,
0.07685180753469467,
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0.09203652292490005,
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0.015554876066744328,
0.000898967613466084,
0.12434011697769165,
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0.10240866243839264,
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0.15619029104709625,
0.12871965765953064,
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-0.006329422816634178,
0.04937028884887695,
0.11585595458745956,
0.10168565809726715,
0.0371277816593647,
0.024809377267956734,
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0.09225110709667206,
-0.06805473566055298,
-0.02025802619755268,
0.05475235357880592,
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0.10875516384840012,
0.04155736789107323,
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-0.009376075118780136,
0.16656018793582916,
-0.0121413329616189,
-0.08386251330375671,
0.010608620941638947,
0.054766926914453506,
0.0030281979124993086,
0.015987811610102654,
-0.033973000943660736,
0.09980865567922592,
-0.05469664931297302,
-0.038453444838523865,
-0.07822733372449875,
0.08728114515542984,
-0.05781242623925209,
0.07860465347766876,
-0.15678532421588898,
-0.06810717284679413,
0.047088202089071274,
0.06654632836580276,
0.2537780702114105,
0.1453673243522644,
0.009567169472575188,
-0.008960607461631298,
-0.03126179799437523,
0.1099853441119194,
0.14933690428733826,
0.03344373032450676,
-0.12339537590742111,
0.059032585471868515,
0.08060459792613983,
-0.07904291898012161,
-0.02328917570412159,
0.14637093245983124,
0.06686343997716904,
0.02294052019715309,
0.012639831751585007,
-0.003967514727264643,
-0.059297990053892136,
-0.10453402996063232,
0.0512024462223053,
-0.06167779862880707,
-0.005080683156847954,
-0.1437113732099533,
0.14254894852638245,
-0.04689862206578255,
0.04513585567474365,
-0.006225928198546171,
-0.024542294442653656,
0.10817473381757736,
-0.13806754350662231,
-0.0626024380326271,
0.12478547543287277,
0.006487169768661261,
0.1058259829878807,
-0.08437231928110123,
0.11898238211870193,
-0.0797075629234314,
-0.004010320175439119
] | Protein zyg-11 homolog A | Homo sapiens | Mammalia | Chordata | ZYG11A | 759 | 2 | 3 | 9,606 | 9,606 | Probably acts as a target recruitment subunit in an E3 ubiquitin ligase complex ZYGA-CUL2-elongin BC | MVHFLHPGHTPRNIVPPDAQKDALGCCVVQEEASPYTLVNICLNVLIANLEKLCSERPDGTLCLPEHWSFPQEVAERFLRVMTWQGKLTDRTASIFRGNQMKLKLVNIQKAKISTAAFIKAFCRHKLIELNATAVHADLPVPDIISGLCSNRWIQQNLQCLLLDSTSIPQNSRLLFFSQLTGLRILSVFNVCFHTEDLANVSQLPRLESLDISNTLVTDISALLTCKDRLKSLTMHYLKCLAMTKSQILAVIRELKCLLHLDISDHRQLKSDLAFHLLQQKDILPNVVSLDISGGNCITDEAVELFIRLRPAMQFVGLLATDAGSSDFFTTKQGLRVAGGASMSQISEALSRYRNRSCFVKEALHRLFTETFSMEVTMPAILKLVAIGMRNHPLDLRVQFTASACALNLTRQGLAKGMPVRLLSEVTCLLFKALKNFPHYQQLQKNCLLSLTNSRILVDVPFDRFDAAKFVMRWLCKHENPKMQTMAVSVTSILALQLSPEQTAQLEELFMAVKELLAIVKQKTTENLDDVTFLFTLKALWNLTDGSPAACKHFIENQGLQIFIQVLETFSESAIQSKVLGLLNNIAEVRELSSKLVTEDVLKHINSLLCSREMEVSYFAAGIIAHLTSDRQLWISRDFQRRTLLQDLHATIQNWPSSSCKMTALVTYRSFKTFFPLLGNFSQPEVQLWALWAMYHVCSKNPSKYCKMLVEEEGLQLLCDIQEHSEATPKAQQIAASILDDFRMHFMNYQRPTLCQMPF |
A2BFL2 | [
-0.07538676261901855,
-0.1633351445198059,
0.030254479497671127,
-0.0808209478855133,
-0.05359387770295143,
-0.00819964986294508,
-0.0173826701939106,
0.1006852388381958,
0.0719759613275528,
0.15386182069778442,
0.010594376362860203,
-0.018387790769338608,
-0.046323925256729126,
-0.03505552187561989,
-0.00693533755838871,
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-0.26701346039772034,
0.04577701538801193,
0.05426696687936783,
0.0014658281579613686,
0.17440907657146454,
0.014867519028484821,
-0.0035053533501923084,
0.13706745207309723,
0.07256380468606949,
0.11639683693647385,
0.07385513186454773,
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-0.08906042575836182,
0.02762218564748764,
0.09201759845018387,
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0.08820024877786636,
-0.01815987005829811,
-0.04737761989235878,
0.017902089282870293,
-0.030779298394918442,
0.10432238131761551,
-0.1091311052441597,
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0.0903768539428711,
-0.07940063625574112,
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0.12784068286418915,
0.10742565989494324,
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0.026958607137203217,
0.09681304544210434,
0.1357351839542389,
0.019622962921857834,
0.03453485295176506,
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0.09628046303987503,
-0.06233765184879303,
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0.049676939845085144,
-0.09261384606361389,
-0.04861888661980629,
0.1227288544178009,
0.015576629899442196,
-0.049254003912210464,
-0.019702503457665443,
0.16612952947616577,
0.006418896373361349,
-0.08953937888145447,
0.03447802737355232,
0.052126068621873856,
0.0316915363073349,
0.012631974183022976,
-0.02319643460214138,
0.08869673311710358,
-0.042621877044439316,
-0.04277893900871277,
-0.06273927539587021,
0.11440789699554443,
-0.04591529071331024,
0.10103492438793182,
-0.14930041134357452,
-0.05580971762537956,
0.053340766578912735,
0.0693303644657135,
0.25722450017929077,
0.14535197615623474,
0.03342362120747566,
0.020346663892269135,
-0.02509775385260582,
0.12113930284976959,
0.1786801964044571,
0.03814776614308357,
-0.10232724249362946,
0.036392804235219955,
0.08614165335893631,
-0.10049786418676376,
-0.046562425792217255,
0.11424937099218369,
0.0804947093129158,
0.02194463647902012,
0.018485724925994873,
-0.00035177767858840525,
-0.07383852452039719,
-0.09150334447622299,
0.026566583663225174,
-0.08307412266731262,
-0.04688306525349617,
-0.13499781489372253,
0.12483436614274979,
-0.05526240915060043,
0.06790833920240402,
-0.022966574877500534,
0.00810057669878006,
0.0911116823554039,
-0.14270047843456268,
-0.05156329646706581,
0.13101232051849365,
0.009298648685216904,
0.09777028113603592,
-0.09605202078819275,
0.11731212586164474,
-0.07045577466487885,
0.028587425127625465
] | Protein zyg-11 homolog A | Mus musculus | Mammalia | Chordata | Zyg11a | 627 | 2 | 1 | 10,090 | 10,090 | Probably acts as a target recruitment subunit in an E3 ubiquitin ligase complex ZYGA-CUL2-elongin BC | MAWQGKLTDRTASIFQGKQMSLKLINIPRVKLSAAAFTKAFCHHKLIEVNATSVDSELLAPDIIHALQSSAWIQKNLQCLVLDSVSIPPNSGLVALSHFTGLHTLSVANVSFCNEDLVSVSQLPNLGSLDISNTLVTNISALLSCKNRLRSLTMHYLKCLAMNSPQVLAVIRQLKCLLHLDISDHQQLRSDLAFYLLQQKDILPNLTSLDISGGTDVTDQAVESFLQHRPAMRFVGLLYTDAGYSDFFTAKQGLKVAGGANMSQISEALSRYRNRSCFVKEALFRLFTETLSLRAVLPVMLKLVAIGMRNHPLDLPVQFTASACALNLTRQELARGMPVRLLAEITDLLFKATKNFPYYQQLQKNCLLSLTSSRILMDVPFDRFDAAKLALRWVCRRESPKLRTMAVSITSILALKLSPEEMGQLQEELIMAIKELLTIIRQKLAENLDDVTFLFTLKALWNLTDECPLACKYFMENEGLATVIRVLETFSISVIQSKVLGLLNNVAEVRELSSKLVTEDVIERIISLLHSSNLEVSFLAAGVLAHLTCDRQHWLSRDLQRTDLLRYLHLAIQNWPSSRCDMSVLVTYRSFKAFSPLLVNFSQPEVQRWALWAIHHVCSKNPRPKDV |
Q9C0D3 | [
-0.05324510112404823,
-0.18582944571971893,
0.0288999006152153,
-0.0856061652302742,
-0.056626543402671814,
-0.005862212739884853,
-0.023093130439519882,
0.12437402456998825,
0.03955719992518425,
0.18571744859218597,
-0.005621836520731449,
-0.03127679228782654,
-0.056109875440597534,
-0.0185431819409132,
-0.004707958549261093,
-0.059017401188611984,
-0.012478086166083813,
-0.0728033110499382,
-0.19538265466690063,
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-0.042226642370224,
-0.2791883051395416,
0.04501933977007866,
0.07267742604017258,
-0.021951710805296898,
0.1413448601961136,
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-0.009103575721383095,
0.13199633359909058,
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] | Protein zyg-11 homolog B | Homo sapiens | Mammalia | Chordata | ZYG11B | 744 | 1 | 2 | 9,606 | 9,606 | Serves as substrate adapter subunit in the E3 ubiquitin ligase complex ZYG11B-CUL2-Elongin BC. Acts to target substrates bearing N-terminal degrons for proteasomal degradation with the first four residues of substrates being the key recognition elements (PubMed:33093214, PubMed:34214466, PubMed:35636250). Prefers Nt-Gly but also has the capacity to recognize Nt-Ser, -Ala and -Cys (PubMed:36496439). Involved in the clearance of proteolytic fragments generated by caspase cleavage during apoptosis since N-terminal glycine degrons are strongly enriched at caspase cleavage sites. Also important in the quality control of protein N-myristoylation in which N-terminal glycine degrons are conditionally exposed after a failure of N-myristoylation (PubMed:31273098). In addition, plays a role in the amplification of cGAS to enhance innate immune response. Mechanistically, strengthens the processes of cGAS binding with dsDNA and assembling oligomers and also accelerates and stabilizes cGAS-DNA condensation, thereby enhancing production of antiviral IFNs and inflammatory cytokines (PubMed:36933219) | MPEDQAGAAMEEASPYSLLDICLNFLTTHLEKFCSARQDGTLCLQEPGVFPQEVADRLLRTMAFHGLLNDGTVGIFRGNQMRLKRACIRKAKISAVAFRKAFCHHKLVELDATGVNADITITDIISGLGSNKWIQQNLQCLVLNSLTLSLEDPYERCFSRLSGLRALSITNVLFYNEDLAEVASLPRLESLDISNTSITDITALLACKDRLKSLTMHHLKCLKMTTTQILDVVRELKHLNHLDISDDKQFTSDIALRLLEQKDILPNLVSLDVSGRKHVTDKAVEAFIQQRPSMQFVGLLATDAGYSEFLTGEGHLKVSGEANETQIAEALKRYSERAFFVREALFHLFSLTHVMEKTKPEILKLVVTGMRNHPMNLPVQLAASACVFNLTKQDLAAGMPVRLLADVTHLLLKAMEHFPNHQQLQKNCLLSLCSDRILQDVPFNRFEAAKLVMQWLCNHEDQNMQRMAVAIISILAAKLSTEQTAQLGTELFIVRQLLQIVKQKTNQNSVDTTLKFTLSALWNLTDESPTTCRHFIENQGLELFMRVLESFPTESSIQQKVLGLLNNIAEVQELHSELMWKDFIDHISSLLHSVEVEVSYFAAGIIAHLISRGEQAWTLSRSQRNSLLDDLHSAILKWPTPECEMVAYRSFNPFFPLLGCFTTPGVQLWAVWAMQHVCSKNPSRYCSMLIEEGGLQHLYNIKDHEHTDPHVQQIAVAILDSLEKHIVRHGRPPPCKKQPQARLN |
Q3UFS0 | [
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] | Protein zyg-11 homolog B | Mus musculus | Mammalia | Chordata | Zyg11b | 744 | 1 | 2 | 10,090 | 10,090 | Serves as substrate adapter subunit in the E3 ubiquitin ligase complex ZYG11B-CUL2-Elongin BC. Acts redudantly with ZER1 to target substrates bearing N-terminal glycine degrons for proteasomal degradation. Involved in the clearance of proteolytic fragments generated by caspase cleavage during apoptosis since N-terminal glycine degrons are strongly enriched at caspase cleavage sites. Also important in the quality control of protein N-myristoylation in which N-terminal glycine degrons are conditionally exposed after a failure of N-myristoylation | MPEDQAHAAMEEASPYSLLDICLSFLTTNLEKFCSARQDGTLCLQEPGVFPQEVADRLLQTIAFHGLLNDGTVGIFRGNQMRLKRACIRKAKISAVAFRKAFCHHKLVELDATGVNADITITDIISGLGSNKWIQQNLQCLVLNSLTLSLEDPYERCFSRLSGLRALSITNVLFYNEDLAEVASLPRLESLDISNTSITDITALLACKDRLKSLTMHHLKCLKMTTTQILDVVRELKHLNHLDISDDKQFTSDIALRLLEQKDILPNLVSLDVSGRKHVTDKAVEAFIQQRPSMQFVGLLATDAGYSEFLMGKGHLKVSGEANETQIAEALRRYSERAFFVREALFHLFSLTHVMEKTKPDILKLVVTGMRNHPMNLPVQLAASACVFNLTKQDLALGMPVRLLADVTHLLLKAMEHFPNHQQLQKNCLLSLCSDRILQDVPFNRFEAAKLVMQWLCNHEDQNMQRMAVAIISILAAKLSTEQTAQLGAELFIVRQLLQIVKQKTNQNSVDTTLKFTLSALWNLTDESPTTCRHFIENQGLELFMRVLESFPTESSIQQKVLGLLNNIAEVQELHSELMWKDFIDHISSLLHSVEVEVSYFAAGIIAHLISRGEQAWTLSRSQRNSLLDDLHSAILKWPTPECEMVAYRSFNPFFPLLGCFTTPGVQLWAVWAMQHVCSKNPSRYCSMLIEEGGLQHLYNIKEHEQTDPYVQQIAVAILDSLEKHIVRHGRPPPCKKQPQARLN |
P21541 | [
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0.07317417860031128
] | Early embryogenesis protein zyg-11 | Caenorhabditis elegans | Chromadorea | Nematoda | zyg-11 | 799 | 1 | 1 | 6,239 | 6,239 | Acts as a target recruitment subunit in the E3 ubiquitin ligase complex zyg-11-cul-2-elc-1. Required for metaphase to anaphase transition and M phase exit at meiosis II. Regulates polarity establishment | MDHNAALTTCSTSAIPRLARLATERIAELIENDALPEFDHKVIASCSNDIFEVLRQKKKLNHQTLQTMCSTSRFQINKIDLMGNKVELQDLELCSNQNLVSFRLGDIDYFPNTNKIQVADVLDTALNRTSRQQLRHLDLSGRHRITSNWPTYVARKLPRLESLAFANRSTANETLSQIGASLLNLRFLDISSTCVTDISCISSLRNLEVLIMYNLNILKGDVTETLSNLTKLRVLDISRKVNTDYLQETSQDAHLDLALGIYNRSVEAIESGTATPWAELRAIDMSGLSIVQFGTDRALAFVEKIIEAHPKLEQISLLATPLDSSLIEIPNRNLQVINTVSRRSIIFALSHYANLDRPAFITHALHSVYYQLQSGYDKFSQEELKECLRLVCISMQQGLNTLPVQIAGSACLYHLCKMKRIKRLSVKEVNNCIERSLDAAEQYRSMTQLQKNVWLTICNDYLLHLDEIDFYRTCKVALDTMLLNRDASVERMTIAIVSIVTPKMRPSEAKILTTETKYVYHLVKIMNDYLEAYTREHRVGHERDNENALYTLKFTLSALWNLTDECPATCKAFLDAGGVQIAFRILKAFDYHGNVQTKVLGILNNLAEVEELHLGQLCKNEYISVLISCLDGSFNEVDSKGRYREVERSYFAAGILANLLTNTDGWESENQRDEACEKLLELIEQYPTLPSAMVSYKSFIPFSRIVRESNSNGAIMWCLWGVHHVLQHREKNKAPTYEKGYIEMFMDSGLSPIVEDMSHGHSKHIHNLDIRVVHLAREIIDIVSCHSLSSSPVRLVRRV |
Q5TYQ1 | [
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0.013921025209128857
] | Protein zyg-11 homolog | Danio rerio | Actinopteri | Chordata | zyg11 | 746 | 2 | 1 | 7,955 | 7,955 | Serves as substrate adapter subunit in an E3 ubiquitin ligase complex zyg11-cul2-elongin BC. Targets substrates bearing N-terminal glycine degrons for proteasomal degradation | MIHLSQTMDKSSLPSLSDLCMSLVSSRLELFCEMRDDGSLSFREPLVFPQELADQLLCKMATDGVLNDSTVGIFRNCQQFRLRHACIRTARISAEAFHRALCPHRLVELDASRVNADLTIADILRGLSSNKSLQESLQRLVLNGLTMSSLEEPSRRCFSAMQGLRALSVSNVDFYDWGLADVCLLPRLESLDISNTSVSNLTPLLGLRSRLRYLTMHQLKRLEMTTAQLLAVLSQLEVLQHLDISDDKQFTSDVARQLLETPGILPQLVSLDVSGRKQVTDAAVKAFVEARPGMTFVGLLATDAGFSEFLSGEGSLKVTGEANETQICEALRRYSEREGFVREALFHLFSLTHAIEKPRPDILKLVALGMKNHPTTLNVQLAASACVFNLTKQELAFGIPVRLLGNVTQQLLEAMKTFPNHQQLQKNCLLSLCSDRILQEVPFNRFEAAKLVMQWLCNHEDQNMQRMAVAIISILAAKLSTEQTAQLGAELFIVKQLLHIVRQKTCQSTVDATLKFTLSALWNLTDESPTTCRHFIENQGLELFIKVLESFPSESSIQQKVLGLLNNIAEVSELHGELMVQSFLDHIRTLLHSPEVEVSYFAAGILAHLTSRGEKVWTLELTLRNTLLQQLHSAILKWPTPECEMVAYRSFNPFFPLLECFQTPGVQLWAAWAMQHVCSKNAGRYCSMLLEEGGLQHLEAITSHPKTHSDVRRLTESILDGLQRHRARTGYTAIPKTQAHREKCNP |
A0JMZ3 | [
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0.039774175733327866,
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0.15143758058547974,
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0.08066210150718689,
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0.0743802934885025,
0.04430846869945526,
0.003712891135364771,
0.006831507198512554,
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0.032414451241493225,
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0.14220187067985535,
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0.05827648937702179,
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0.08706995844841003,
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0.12449490278959274,
0.007138407323509455,
0.0933038666844368,
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0.10266415774822235,
-0.05469130352139473,
0.02624514140188694
] | Protein zyg-11 homolog | Xenopus laevis | Amphibia | Chordata | zyg-11 | 732 | 2 | 1 | 8,355 | 8,355 | Serves as substrate adapter subunit in an E3 ubiquitin ligase complex zyg11-cul2-elongin BC. Targets substrates bearing N-terminal glycine degrons for proteasomal degradation | MEESSPKSLLDITLLYLSTHLEKFCWERQDGTYCLQDAAIFPQEVADRLLQAMAVQRQLNEVTVGIFRGNQLRLKRACIRKAKISAVAFRKAFCHHKLIELDATGVNADITITDIISGLSSSKWIRENLQCLVLNSLTLSLEDPYERCFSQLSGLRVLSITNVLFYNEDLADVASLPRLESLDISNTSVTDITALVACKDILKSLTMHHLKCLKMTTTQILEVIRELKKLNHLDMSDDKQFTSDIACRLLEQNDILLHLVSLDISGRKHVTDKAVEAFIRHRPQMQFVGLLATEAGYSEFLSGEGCVKVSGEANQTQIAEALRRYSERSFFVREALFHLFSLTHVMDKANPEMLKLVVIGMRNHPTNLPVQLAASACVFNLTKQDLAAGMPVKLLADVTHLLLEAMKHFPNHQQLQKNCLLSLCSDRILQDVPFNRFDAAKLVMQWLCNHEDQNMQRMAVAIISILAAKLSTEQTAQLGAELFIVRQLLQIVRQKTSQNMVDTTLKFTLSALWNLTDESPTTCRHFIENQGLELFMKVLETFPSESSIQQKVLGLLNNIAEVKELHTELMCKDFIDQISKLLHSVEVEVSYFAAGIIAHLVSRGEETWTLSSSMRETLLEQLHSAILSWPTPECEMVAYRSFNPFFPLLACFRTPGVQLWAVWAMQHVCSKNPVRYCSMLIEEGGLVRLHRIRDHMCADPDVLRITITILDNLDRHLKKHGNPPCQKPPFTK |
Q621J7 | [
-0.011104372330009937,
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0.00047877099132165313,
-0.13960808515548706,
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0.23055998980998993,
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0.081812284886837,
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0.0894523561000824,
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0.04631921276450157,
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0.07112695276737213,
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0.1253698766231537,
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0.0873492956161499,
0.05917410925030708,
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0.10376092046499252,
0.045988332480192184,
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0.049071989953517914,
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-0.005139670800417662,
0.0656265914440155,
0.048981841653585434,
0.013483194634318352,
-0.03203311562538147,
0.0820143073797226,
-0.1574573963880539,
-0.06742005795240402,
-0.06750869750976562,
0.12415158748626709,
-0.047106947749853134,
-0.06705492734909058,
0.07565908879041672,
-0.06759386509656906,
0.01293521374464035,
-0.06574112176895142,
0.0013581305975094438,
0.024961652234196663,
0.1735023558139801,
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-0.02868182584643364,
0.043203771114349365,
-0.21640552580356598,
0.018206410109996796
] | Probable serine/threonine-protein kinase zyg-1 | Caenorhabditis briggsae | Chromadorea | Nematoda | zyg-1 | 709 | 3 | 1 | 6,238 | 6,238 | Protein kinase that plays a central role in centrosome duplication. Paternal copy is required to regulate synthesis of daughter centrioles prior to fertilization. Maternal copy regulates centrosome duplication during later cell cycles. Functions upstream of sas-5 and sas-6, and is required for their localization to the centrosome (By similarity) | MSGGKSGTKLSSFQNLQQIGQGGFGVVYSAQRENGEKVAIKKIGNAASQTRIKEEIKTMKLLRHRNIVQFYETFFENGETYLVMELCEGGSLMDYVKQKGPLDDSTAVHILRQLIAAVKYIHDENILHRDLSAGNVFIKDATKSTITVKLGDFGLATNLGQHGTACTIVGTPGFIAPQVFGQNYDQAADVYSLGAVLYTMLTKHTPPTKGPPNLESLKKRNPSAADLVERMMHTDARRRIQLKEIVMTDYVKAKMGEATPGSREHSRDSRSQRSREPFRSSRDGISLERRPPARSSSQPVNSRRDPDGYRAAHEMPTTSRTSVEPDRARVRHRLSARGIGSSQEDDLRQQIWPIRMERLVGQRVRTPGGRYIVEMNTRCRFEVVSKGNIVLRILVVEYDPHLLIQTVYVHKMSNRVEHARNETDDLIELTRSPISYTSLSQLPKEVMNDYMRLEKMMVSTIASRVAKITHRRPSQFPDASAQLMENGDLRIRFPNSLIVRRKSNGEVHNYIDGFANNKEEVRGLQLSKVREVYACLTQLEQCLSRMNPTMKILPMVFSAGPDIVATYNNSPSSILPSTSSQASRFPFSEISSSQQLVPHSAPIPNKPLSSRTTSSLNVRNGVSSDENTAPAATRQKYKARLDPVTGRIVSVQAEDNRKLRCSTSKPDQFIFTDPSISSSEQRFMRNGRVPERASEMLHALLVYMKKKQN |
Q9GT24 | [
0.0210875254124403,
-0.05174205079674721,
-0.04999848082661629,
-0.012255086563527584,
-0.09682725369930267,
0.03845605254173279,
0.06737414002418518,
0.0063919490203261375,
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0.26280343532562256,
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0.030083362013101578,
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0.04528297111392021,
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0.21716414391994476,
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0.09625951945781708,
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0.0276749636977911,
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0.05804439261555672,
0.08088701218366623,
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0.08892392367124557,
0.05456132814288139,
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0.062020961195230484,
-0.09030312299728394,
0.013494396582245827,
0.07363653928041458,
0.014709582552313805,
0.000504279334563762,
-0.06565828621387482,
0.09402608871459961,
-0.1606769859790802,
-0.017976684495806694,
-0.08946828544139862,
0.12343592196702957,
-0.03760097175836563,
-0.059447597712278366,
0.04047420620918274,
-0.08679107576608658,
-0.005839785095304251,
-0.01253494992852211,
-0.009372700937092304,
0.030197180807590485,
0.17584241926670074,
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-0.02413731999695301,
0.03188665956258774,
-0.19563241302967072,
0.007148046977818012
] | Probable serine/threonine-protein kinase zyg-1 | Caenorhabditis elegans | Chromadorea | Nematoda | zyg-1 | 706 | 1 | 1 | 6,239 | 6,239 | Protein kinase that plays a central role in centrosome duplication, control of centrosome size, spindle formation and nuclear envelope breakdown during cell divisions (PubMed:11371350, PubMed:15232593, PubMed:15665853, PubMed:18765790, PubMed:19081077, PubMed:19109417, PubMed:22623721, PubMed:27689799). Paternal copy is required to regulate synthesis of daughter centrioles prior to fertilization (PubMed:11371350, PubMed:18765790). Maternal copy regulates centrosome duplication during later cell cycles (PubMed:11371350, PubMed:18765790). Functions upstream of sas-5 and sas-6, and is required for their localization to the centrosome (PubMed:15232593, PubMed:15665853). Its role in nuclear envelope breakdown is mediated by the spindly-like protein spdl-1 and the RZZ complex, which in turn recruits the spindle checkpoint proteins mdf-1 and mdf-2, dynein and dynactin to unattached kinetochores (PubMed:18765790, PubMed:18936247) | MSGGKSGSRLSAYSHLKEIGKGGFGVVYAAQRENGEKVAIKRIDKKVPKNRVWTEIQTMKELKKSKYVVEFYEDFVEDGYTYIVMELCEGGSLQAYVREHGALDDATAVHVLRQLISAVSFMHRVNVIHRDLSAGNVFIKDSKKKKMTVKLGDFGLATTLGRGETTCTIVGTPGFIAPQVYDQEYTQSADVYSLGAVLYTMLTARNPPPKGLPPTCGMSPNAARLVEQMMDTDAKKRIPLTQIVLSEFMYENTNENAVIFSREHSRDGRRQRSREPVRSSRDDRSRDGRALIRSSSQPAHSGRAPLSNRPIHDRMPSTSSRGFDSERGRERDRDSGRGTVPPSREDRNRSQLWPIRMDRLEGQRVCTAGGRYIVELDTRCRFEVAAQGNFVKRILIVEVDEMVQTVYVHRIPDRTVRGRNGEEELITLTNNPFVYTSYSQMPKEVQNDYMRLQKMVAVTISGRVAKVTFRRPSQFPDAQAQLMENGDLRIKLPRSVIVRKMDNGEIFNCIDGIATQKQAVSGITLTKVNEVYKYLIRFEQCLNGMDRGMVCFPIVFSAGTNMVGSSPSSLMPSGSSQTSRFPFSNLSNNQPSLVPHSAPFLTKPTSSQRASSANVQRRVSTDENSSPSVAPSKYKIKIDPTTQKVRSIQATDGRVLRCSTSKADQFIFTDPAIRPDDQRFMRTDRVPDRASEMLHTLCERMRKLHQ |
Q76N59 | [
-0.05909602344036102,
0.020622283220291138,
0.023609448224306107,
-0.10544489324092865,
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0.13565640151500702,
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0.01609601080417633,
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0.14433443546295166,
0.09245286136865616,
0.044999558478593826,
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0.04534227028489113,
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0.08050533384084702,
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] | Zygote formation protein zyg1 | Dictyostelium mucoroides | Eumycetozoa | Evosea | zyg1 | 268 | 2 | 1 | 31,287 | 31,287 | Plays an essential role in zygote formation by inducing sexual cell fusion. Overexpressing cells eventually formed many loose mounds, in which giant multinucleate cells were surrounded by normal-sized cells | MEIDSKITNFEDAGTINLNLHNFVSEKFANKPKVLNVASLASNSVDEAGDSEQKVSFRINQTGNIFYSTTTPELTLESKKLFNSVTVLFAAMTKALGEKGLNLFNYEAVASLIQKSGYFVEVQKFQKNLSIKSGSLSIDTQIIQQLIPGLTSGASLDIAKGVLGALNGEFSASSSDEKVKIAHLLFICEELFGAPSVTVRLFYATKETHKTLTSSPCHKSSSVSFELNQEASTFLFVSPDTIAEFSQKFETQPEEYKNLIEKLKGYLP |
G5EEM5 | [
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] | Zygote defective protein 9 | Caenorhabditis elegans | Chromadorea | Nematoda | zyg-9 | 1,415 | 1 | 1 | 6,239 | 6,239 | Plays a major role in organizing microtubules and spindle poles during mitosis and meiosis in one-cell stage embryos (PubMed:16971515). Required for default nucleus positioning in oocytes (PubMed:16971515) | MSNWDYLDEVDILPKLPPNFDELRESKKWQERKEALEALLKVLTDNERLSTKASYAELIGHLQMVLAKDANINCQALAAKCIGKFATGLRAKFSSFAGPLLPVIFEKMKEKKPMLREPLVDCSNEVGRTMQSLETGQEDILAALAKPNPQIKQQTALFVARQLDLVVPAKQPKGFIKAVVPVFGKLTGDADQDVREASLQGLGAVQRIIGDKNVKNLLGDASSDEGKMKKIGEYAEKSTASFAEEQAKNAPPVAPTSSTPSASAASGDPSGGTATAVVSSGAPVAEADPWDFLDAFDVLSKMPDGFDTNIESKKWQERKEALEGLLQLITANPKLDPKANYGALVERLQKVLEKDANINVAALAANCITGIANGLRTKFQPFAVSVTPIIFEKFKEKKPTLRDPLVACIDAVVATTNLEAVGEIVLAALGKPNPSIKTQTDLFLQRCFMKLNSQTMPKKTLKTLIPSLIKHSGDSDSEVREASYAAMGAMMRAIGEKPSLQLLADIASDNLKMSKIKEFHQKALDEAGPAEIAEMVKSIHKADAPPAAAPPKKTAPPKKQPEDEEVVEEEDEPLKPPPGDKKKKVPVKENEENEPPVVAPKAELLLSDNEDKKQRIKEEKQLKLVKWNFQAPTDEHISQLQTLLGNQAKVSLMSQLFHKDFKQHLAALDSLVRLADTSPRSLLSNSDLLLKWCTLRFFETNPAALIKVLELCKVIVELIRDTETPMSQEEVSAFVPYLLLKTGEAKDNMRTSVRDIVNVLSDVVGPLKMTPMLLDALKSKNARQRSECLLVIEYYITNAGISPLKSLSVEKTVAPFVGDKDVNVRNAAINVLVACFKFEGDQMWKAAGRMADKDKSLVEERIKRTGVKPGSGVVTSPPTGGPKILVPQQQGSVVRRPASRSRTREPEPEEVQSDTFTIRQDTMPPKTSSRYALRDDVFSSAMGRLDGTQVITPPQPVNGWSNNTFQMKRTNSSSSISSIDTSDQIQRSINNISSSLADVAQDAMFQVTYVLNQPEQRHLVDRRADLVFRASAAQLDLVIEEFNAGRDVSGTMDACTQMLFILMGGVETEHGLEPLNASPDTVKAIISSVLRCIIQIGNTESGYGMARSLNRLAMRLIYRVELSNLLCGLILAMTESLQMNTGITELVSKLSSKWCDELEKRRAQLRASDIVDSFNAFYVCALTELKMDISDSHILIVDNYLERVILQQGDVVLDAARRLSRPHMHLTSMINKILQMMRERKIDPIMPGTLEARMPQEDEAVVVRSGVQVSIDNILRDTSMAVKHIEQLNILIASSDRSWNEYMEYLKNNPMGELIKELVGECSRKKRIDFNLSHVVKSSMAVFKAMAATGPVQEEGRITPTDINRMDTMIVGTPLSRGDATITRARGNMIRPKRTTLSRDQMANIRHTLDRVKNH |
Q9UTC0 | [
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] | Metallothionein zym1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | Schizosaccharomycetes | Ascomycota | zym1 | 50 | 1 | 1 | 284,812 | 284,812 | Metallothionein involved in tolerance to zinc and cadmium. Binds four zinc ions | MEHTTQCKSKQGKPCDCQSKCGCQDCKESCGCKSSAVDNCKCSSCKCASK |
Q8GSP8 | [
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] | Zygote-specific protein 3 | Chlamydomonas reinhardtii | Chlorophyceae | Chlorophyta | ZYS3 | 371 | 2 | 1 | 3,055 | 3,055 | May have a role in the remodeling of the endoplasmic reticulum upon zygote formation | MLRSAGRVAAVALLALFALGCVSAAAKPSTDRLVAAIKSKNLSAVVDALSVKGLDVNTPDSTRRLPLVEAARSRDARLVGALLDQGALARVSDGTTTPLHLSMQGGSAAIVKLLLAHGADPNAKDKTGASARSTAAAVKELADLLKQWDARGAMAFEDEPGAWIREERDGQSYYWKPANGESRWAVPPSCAWQRVTVQGHPIKYINSLTGQETTRVPPALAWARVTAADGSALWLNWASRVASAAATAPAELPAELAAELAMHPNRRWYNTATREYVYTDPAYATPWRELVDEASGAPFFFNVETGDTTWELPAALAWTEVIESSSGADGESGSGSEAGPRYFHNTVSGEVAWSAPEGSRHVFVEASAADL |
Q9U3F4 | [
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] | Zyxin | Caenorhabditis elegans | Chromadorea | Nematoda | zyx-1 | 603 | 1 | 1 | 6,239 | 6,239 | Functions both as a mechanical stabilizer (via LIM domains) of focal adhesions, and as a sensor component for muscle cell damage (via N-terminus) (PubMed:23427270). Regulates, stabilizes and maintains posterior lateral mechanosensory (PLM) synaptic branch extension and new synapse formation and growth during larval development (PubMed:25252943) | MGPPPPPPPPPLLPSGEILPSRKWKTEDAPRRNNHPAPAPPKPSRPTVDASALQHAAARLRKTGYNEPVRGDVENLSDGRLDRPHQQLPDGDRTYRANLQQLAQPKTRAEIPSPPTYSNQPRPLGDFHRDPNALSQFQQSREALLSSTSPTSNYSPINKFSSSTLTQYANKSPSPPSFGNSNSEATYVSPYSSKHSYPTNFRSYHKDDDYFNNTATTATTTTSSNSLNENNNSNKYGNKETVLQWSEPYDPSKIRRSQSPIRNAREMIHEYSTTNYVTEVQQPPPPPPDLYQRMTQARTFLQNSLAKQLRDEGLTESQKAANRNQTGALSASSSIPFDASQIVKNSYNGDEVDHLVHQMRTKLNQPADTSPSIVQYPRRQAPDSSRANYSATTSTSFSSSTTRKIMNINICVGCGKEITGDQPGCNAMNQIFHVDCFKCGQCSKTLAGASFYNIDDKPTCEGCYQNSLEKCTACNRAISDKLLRACGGVYHVNCFVCFSCKKSLDGIPFTLDKDNNVHCVPCFHDKFAPRCALCSKPIVPQDGEKESVRVVAMDKSFHVDCYKCEDCGMQLSSKLEGQGCYPIDNHLLCKTCNGNRLRVVSST |
Q04584 | [
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] | Zyxin | Gallus gallus | Aves | Chordata | ZYX | 542 | 1 | 1 | 9,031 | 9,031 | Adhesion plaque protein. Binds alpha-actinin and the CRP protein. May be a component of a signal transduction pathway that mediates adhesion-stimulated changes in gene expression | MASPGTPGTRMTTTVSINISTPSFYNPQKKFAPVVAPKPKVNPFKTGGTSESSQPQPPGTGAQRAQIGRVGEIPVSVTAEELPLPPPPPPGEELSFSSNCAFPPPPPPFEEPFPPAPDEAFPSPPPPPPPMFDEGPALQIPPGSTGSVEKPLAPKAHVEISSAPRDPTPPFPSKFTPKPSGTLSSKPPGLDSTPAPAPWAAPQQRKEPLASVPPPPSLPSQPTAKFTPPPVASSPGSKPGATVPMAPSNSTRYPTSLQTQFTAPSPSGPLSRPQPPNFTYAQQWERPQVQEKPVPTEKSAAVKDMRRPTADPPKGNSPLTMKEVEELELLTQKLMKDMDHPPPVEAATSELCGFCRKPLSRTQPAVRALDCLFHVECFTCFKCEKQLQGQQFYNVDEKPFCEDCYAGTLEKCSVCKQTITDRMLKATGNSYHPQCFTCVMCHTPLEGASFIVDQANQPHCVDDYHRKYAPRCSVCSEPIMPEPGKDETVRVVALEKNFHMKCYKCEDCGRPLSIEADENGCFPLDGHVLCMKCHTVRAKTAC |
Q15942 | [
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] | Zyxin | Homo sapiens | Mammalia | Chordata | ZYX | 572 | 1 | 1 | 9,606 | 9,606 | Adhesion plaque protein. Binds alpha-actinin and the CRP protein. Important for targeting TES and ENA/VASP family members to focal adhesions and for the formation of actin-rich structures. May be a component of a signal transduction pathway that mediates adhesion-stimulated changes in gene expression (By similarity) | MAAPRPSPAISVSVSAPAFYAPQKKFGPVVAPKPKVNPFRPGDSEPPPAPGAQRAQMGRVGEIPPPPPEDFPLPPPPLAGDGDDAEGALGGAFPPPPPPIEESFPPAPLEEEIFPSPPPPPEEEGGPEAPIPPPPQPREKVSSIDLEIDSLSSLLDDMTKNDPFKARVSSGYVPPPVATPFSSKSSTKPAAGGTAPLPPWKSPSSSQPLPQVPAPAQSQTQFHVQPQPQPKPQVQLHVQSQTQPVSLANTQPRGPPASSPAPAPKFSPVTPKFTPVASKFSPGAPGGSGSQPNQKLGHPEALSAGTGSPQPPSFTYAQQREKPRVQEKQHPVPPPAQNQNQVRSPGAPGPLTLKEVEELEQLTQQLMQDMEHPQRQNVAVNELCGRCHQPLARAQPAVRALGQLFHIACFTCHQCAQQLQGQQFYSLEGAPYCEGCYTDTLEKCNTCGEPITDRMLRATGKAYHPHCFTCVVCARPLEGTSFIVDQANRPHCVPDYHKQYAPRCSVCSEPIMPEPGRDETVRVVALDKNFHMKCYKCEDCGKPLSIEADDNGCFPLDGHVLCRKCHTARAQT |
Q62523 | [
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] | Zyxin | Mus musculus | Mammalia | Chordata | Zyx | 564 | 1 | 2 | 10,090 | 10,090 | Adhesion plaque protein. Binds alpha-actinin and the CRP protein. Important for targeting TES and ENA/VASP family members to focal adhesions and for the formation of actin-rich structures. May be a component of a signal transduction pathway that mediates adhesion-stimulated changes in gene expression (By similarity) | MAAPRPPPAISVSVSAPAFYAPQKKFAPVVAPKPKVNPFRPGDSEPPVAAGAQRAQMGRVGEIPPPPPEDFPLPPPPLIGEGDDSEGALGGAFPPPPPPMIEEPFPPAPLEEDIFPSPPPPLEEEGGPEAPTQLPPQPREKVCSIDLEIDSLSSLLDDMTKNDPFKARVSSGYVPPPVATPFVPKPSTKPAPGGTAPLPPWKTPSSSQPPPQPQAKPQVQLHVQPQAKPHVQPQPVSSANTQPRGPLSQAPTPAPKFAPVAPKFTPVVSKFSPGAPSGPGPQPNQKMVPPDAPSSVSTGSPQPPSFTYAQQKEKPLVQEKQHPQPPPAQNQNQVRSPGGPGPLTLKEVEELEQLTQQLMQDMEHPQRQSVAVNESCGKCNQPLARAQPAVRALGQLFHITCFTCHQCQQQLQGQQFYSLEGAPYCEGCYTDTLEKCNTCGQPITDRMLRATGKAYHPQCFTCVVCACPLEGTSFIVDQANQPHCVPDYHKQYAPRCSVCSEPIMPEPGRDETVRVVALDKNFHMKCYKCEDCGKPLSIEADDNGCFPLDGHVLCRKCHSARAQT |
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] | Zyxin | Xenopus laevis | Amphibia | Chordata | zyx | 663 | 1 | 1 | 8,355 | 8,355 | Adhesion plaque protein. May be a component of a signal transduction pathway that mediates adhesion-stimulated changes in gene expression (By similarity). Suppresses the transcription-repressing activity of hesx1/anf1 | MDPAAPATRMTSSFTINISTPSFYNPPKKFAPVVPPKPKINPFKAPEEPQSLVPQENSAGPGLHQAFVGKVGEMPPGVDHDDFVLPPPPPSEESISPPSSSFPPPPPSFGDEGLGSPSGGSFPPPPPPEFSEPFPPPIEEFFPSPPPLEECVSDTQDLPVPVPPPPPPPLPSPPAAPPPKPSAPCEAPKPAPVFPKSSPPPAFPKPEPPSVAPKAASSIFIPKPSAPMAVAPKPLAPPPVAAKPSGPVSFAPPSPAPHTFSPDPSAPAHTFSPKTVTFSPKSAPHTFMPKPSAPVTYPQKTTEPPAEASQSSPKVTPAAKHEAPPPTVPSGGRAPGFSFAQQRERPRVLEKPRANLQGSEPEHEPTVEVQVERTRSLGPQTESGRSPGAQSTGGKDMKPLPEGLRSQKPMSDGIHRTGGQHSGHKVTGQQDQTLGSQGLNMKEVEELEMLTQQLMREMDKPPTAEAHSMELCGFCGRGLSRTETVVRAGEHLYHVACFTCSRCDQQLQGQQYYESAGKPLCDECYQDTLECCAVCDKKITERLLKAIGKSYHPSCFTCAVCKCSLQGEPFIVDDNKLPHCVNDYHRRYAPRCCVCGDPIAPEPGRDETVRVVALEKNFHMMCYKCEDCGCPLSIEADDAGCFPLDGHVLCKKCHTVRARAALG |
Q0VA45 | [
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] | Zyxin | Xenopus tropicalis | Amphibia | Chordata | zyx | 674 | 2 | 1 | 8,364 | 8,364 | Adhesion plaque protein. May be a component of a signal transduction pathway that mediates adhesion-stimulated changes in gene expression. Suppresses the transcription-repressing activity of hesx1/anf1 (By similarity) | MDPAAPAARMTSSFTINISTPSFYNPPKKFAPVVPPKPKVNPFRAAEEPVPQENSAGPGLRRAFVGKVGQIPSMAPPGGDPEDFVLPPPPPNEEPMSPPGSSFPPPPPSFGDDGPGSPLGLFPPPPPPEFSEPFPPPIEESFPSPPPLEEAAGLSDTQDPPASVPPPPPPLPSPPEPAPPVLCEAPKPAPVLPKPPPPSAFPKPEPPQSVAPKAQSSIFIPKPSPPSAVAPKPVAPPPVAAKPSGPGPFVGPSAAPPTHTPAPPAPAHTFSPKPVAGPTFAPKSASHTFMAKPSAPVFSPKAATEPPTEAPQERFPASQSSPKLTPAAKHEAPPPAAKHEAPPPASATRAPGFSFAQQRDKPRVLEKPRANVRDLVPEPPVETRGERTLGPQAEGGRSFGAQPIGGKDTKPLPEGLRNQTPDGTHRVGGQPGTHRPTPHQDQTSGSQGLNMKEVEELEMLTQQLMQEMDKPTPAAEAHTMELCGFCGRGLSRTETVVRAGEHLYHVTCFTCSKCEQQLQGQQYYESAGKPLCEECYQDTLECCAVCEKKITERLLRAIGQAYHPSCFTCAVCKCSLQGEPFIVDDNKLPHCVSDYHRRYAPRCTVCGDPIAPEPGRDETVRVVALEKNFHMMCYKCEDCGCPLSIEADDGGCFPLDGHVLCKKCHTVRARAALG |
O43149 | [
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] | Zinc finger ZZ-type and EF-hand domain-containing protein 1 | Homo sapiens | Mammalia | Chordata | ZZEF1 | 2,961 | 1 | 6 | 9,606 | 9,606 | Histone H3 reader which may act as a transcriptional coactivator for KLF6 and KLF9 transcription factors | MGNAPSHSSEDEAAAAGGEGWGPHQDWAAVSGTTPGPGVAAPALPPAAALLEPARLREAAAALLPTPPCESLVSRHRGALFRWLEERLGRGEESVTLEQFRELLEARGAGCSSEQFEEAFAQFDAEGDGTVDAENMLEALKNSSGANLQGELSHIIRQLQACSLVPGFTDIFSESKEGLDIHSSMILRFLHRNRLSSAVMPYPMLEHCNNMCTMRSSVLKESLDQLVQKEKESPGDLTRSPEMDKLKSVAKCYAYIETSSNSADIDKMTNGETSSYWQSDGSACSHWIRLKMKPDVVLRHLSIAVAATDQSYMPQQVTVAVGRNASDLQEVRDVHIPSNVTGYVTLLENANVSQLYVQINIKRCLSDGCDTRIHGLRAVGFQRVKKSGVSVSDASAIWYWSLLTSLVTASMETNPAFVQTVLHNTQKALRHMPPLSLSPGSTDFSTFLSPNVLEEVDSFLIRITSCCSTPEVELTLLAFALARGSVAKVMSSLCTITDHLDTQYDASSLILSMASVRQNLLLKYGKPLQLTLQACDVKGKEDKSGPENLLVEPWTRDGFLTETGKTRASTIFSTGTESAFQVTQIRIMVRRGGIGAQCGLVFAYNSSSDKFCAEEHFKRFEKYDKWKLQELRQFVKSRIGCSSDDLGEDDPIGWFELEEEWDEADVKLQQCRVAKYLMVKFLCTRQESAERLGVQGLTISGYLRPARAEAEQSVTCAHCRKDTEESVCGATLLLRTLQFIQQLAHDLVQQKESGLKYKSFLDFAGLDLQIFWNFYSKLKQNPREECVSAQTLLLQLLQSCFSVLQGDVLAASEEEKAPIQSPKGVEAAKELYTHLCDVVDKVDGDSVPMEILKQEVRNTLLNGAAIFFPNRQTRRNHLFTMMNVTEQEHKQSLQLTFRSLCTYFSDKDPGGLLLLPEKNDLAKMNISEVLAVMDTLVSVAARECELLMLSGAPGEVGSVLFSLFWSVQGSLLSWCYLQLKSTDSGAKDLAVDLIEKYVGQFLASMRAILESLFSQYSGKTIVERLCNSVFSMAARQLVIFLLDFCTLDIPHCVLLREFSVLTELLKKLCSGPEGGLRKLDVETWQQEQPVVLHTWTKESAHNYENNCHEVSVFVSPGATYFEVEFDDRCETEKRYDYLEFTDARGRKTRYDTKVGTDKWPKKVTFKAGPRLQFLFHSDSSHNEWGYKFTVTACGLPDVAVSWGLDLQLLVSRLMGRLASQCMALKSVRQLGSNMVVPQAKMALVLSSPLWKPVFRHQVCPELELEASWPTHPHRNSKEVKNIPDDPCRHFLLDFAQSEPAQNFCGPYSELFKGFIQACRKQAPKTDIVAGSTIDQAVNATFAALVYRTPDLYEKLQKYVNSGGKIALSEEFAQVYSLADGIRIWMLEMKQKSLMSLGNEAEEKHSSEATEVNPESLAKECIEKSLLLLKFLPTGISSKESCEKLETADETSHLQPLNKRQRTSSVVEEHFQASVSPTEAAPPATGDQSPGLGTQPKLPSSSGLPAADVSPATAEEPLSPSTPTRRPPFTRGRLRLLSFRSMEEARLVPTVKEKYPVLKDVMDFIKDQSLSHRSVVKVLSLRKAQAQSILEVLKITQHCAESLGQPHCFHPPFILFLLELLTCQKDFTNYFGHLEGCGADLHKEIRDTYYQLVLFLVKAVKGFSSLNDRSLLPALSCVQTALLHLLDMGWEPNDLAFFVDIQLPDLLMKMSQENISVHDSVISQWSEEDELADAKQNSEWMDECQDGMFEAWYEKIAQEDPEKQRKMHMFIARYCDLLNVDISCDGCDEIAPWHRYRCLQCSDMDLCKTCFLGGVKPEGHGDDHEMVNMEFTCDHCQGLIIGRRMNCNVCDDFDLCYGCYAAKKYSYGHLPTHSITAHPMVTIRISDRQRLIQPYIHNYSWLLFAALALYSAHLASAEDVDGEKLDPQTRSSATTLRSQCMQLVGDCLMKAHQGKGLKALALLGVLPDGDSSLEDQALPVTVPTGASEEQLEKKAVQGAELSEAGNGKRAVHEEIRPVDFKQRNKADKGVSLSKDPSCQTQISDSPADASPPTGLPDAEDSEVSSQKPIEEKAVTPSPEQVFAECSQKRILGLLAAMLPPLKSGPTVPLIDLEHVLPLMFQVVISNAGHLNETYHLTLGLLGQLIIRLLPAEVDAAVIKVLSAKHNLFAAGDSSIVPDGWKTTHLLFSLGAVCLDSRVGLDWACSMAEILRSLNSAPLWRDVIATFTDHCIKQLPFQLKHTNIFTLLVLVGFPQVLCVGTRCVYMDNANEPHNVIILKHFTEKNRAVIVDVKTRKRKTVKDYQLVQKGGGQECGDSRAQLSQYSQHFAFIASHLLQSSMDSHCPEAVEATWVLSLALKGLYKTLKAHGFEEIRATFLQTDLLKLLVKKCSKGTGFSKTWLLRDLEILSIMLYSSKKEINALAEHGDLELDERGDREEEVERPVSSPGDPEQKKLDPLEGLDEPTRICFLMAHDALNAPLHILRAIYELQMKKTDYFFLEVQKRFDGDELTTDERIRSLAQRWQPSKSLRLEEQSAKAVDTDMIILPCLSRPARCDQATAESNPVTQKLISSTESELQQSYAKQRRSKSAALLHKELNCKSKRAVRDYLFRVNEATAVLYARHVLASLLAEWPSHVPVSEDILELSGPAHMTYILDMFMQLEEKHEWEKILQKVLQGCREDMLGTMALAACQFMEEPGMEVQVRESKHPYNNNTNFEDKVHIPGAIYLSIKFDSQCNTEEGCDELAMSSSSDFQQDRHSFSGSQQKWKDFELPGDTLYYRFTSDMSNTEWGYRFTVTAGHLGRFQTGFEILKQMLSEERVVPHLPLAKIWEWLVGVACRQTGHQRLKAIHLLLRIVRCCGHSDLCDLALLKPLWQLFTHMEYGLFEDVTQPGILLPLHRALTELFFVTENRAQELGVLQDYLLALTTDDHLLRCAAQALQNIAAISLAINYPNKATRLWNVEC |
Q5SSH7 | [
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0.16542932391166687,
0.1425153911113739,
0.003204491687938571,
-0.015905864536762238,
-0.043772898614406586,
-0.01102130115032196
] | Zinc finger ZZ-type and EF-hand domain-containing protein 1 | Mus musculus | Mammalia | Chordata | Zzef1 | 2,924 | 1 | 2 | 10,090 | 10,090 | Histone H3 reader which may act as a transcriptional coactivator for KLF6 and KLF9 transcription factors | MGNAPSNSSEDEAAAAGGEGWSPHQDWAADSGTTPGPGPAAAVLPSAAALLEPARLREAAAALRPAPPCESLVSRHHGALLRWLEERLGRGEESVTLEQFRELLEARGAGCSGEQFEEAFAQFDAEGDGTVDAENMLEALKNSSGANLQGELSHVIRQLQACSLVPGFIDIFSESKEGLGIHSSMILRFLHRNRISSMVIPYPMLDHCNNMCTMRSSVLKESLDQLVQKEKESPGDLARSPEMDKLKSVTKCYAYIETSSNPADIYRMTNGETSSYWQSDGSARSHWIRLKMKPDVVLRHLSIAVAATDQSYMPQQVTVAVGRSASDLQEVRDVHIPSNVTGYVTLLENANISQLYVQINIKRCLSDGCDTRIHGLRAVGFQRVKKSGVSVSDASAIWYWSLLTSLVTASMETNPAFVQTVLHNTQKALQHMPPLSLSPGSTDFSTFLSPNVLEEVDSFLIRITSCCSTPEVELTLLAFALARGSIAKVMSSLCTITDHLDTQYDASSLISSMASVRQNLLLKYGKPLQLTLQACDVKGKEDKSGPENLLVEPWTRDGFLTETGKTRASTIFSTGSDSAFQVTQIRIMVRRGGIGAQCGLVFAYNSPSNKFHAEEHFKRFEKYDKWKLQELRQFVKSRIGCSSDDLGEDDPIGWFELEEEWDEADVKLQQCRVAKFLMVKFLCTRQESAERLGVQGLSISGYLRPARAEAEQSILYAHCRRDTENIHGATLLLRTLQFIQQLSHDLMQQKESGLKHKSFLDFAGLDLQIFWKFYSKLKQNRREECICAQTLLLKLLQSCFSVLQGDPQAASEEEKPTAQRSEGIQAAKELYTHLCNVVDKPNGNSMPMEILKQEVRNTLLNGAAIFFPDRQTRRSQLFTMMKSVTEHERKQSLQLTFHSLCTYFSDKDPGGLLLLPEKSDLATMNTSEVLAVMNTLLSVAARECELLMLNRSHGAVGSVLFSLFWSVQGSLLSWCFLQLKSTDAAAKELAMDLIEKYVGQFLASMRVILESLLSQYSGKTIVEKLCNSVFSMAARQLVIFLLDFCTLDVSHCTLLREFSTLTELLKKLCSDPEGGLSKLDVETWQQEQPVVLHTWTKESTHNYENNCHEVSVFISPGATYFEVEFDERCETEKRYDYLEFTDSRGGKTRYDTKVGTYKWPKKVTFKDGPRLQFLFHSDSSNNEWGYKFTVTAYGLPDVAVSWGLDLQLLVSRLMGRLASQCMALKSVHQLGSNMAVSQAKLTSVLNSPLWKPVFRHQICPELELEASWPTHPHKDGKEVKNIPDDPCRHFLLDFAQSEPAQNFCGPYSELFKGFIQACRKQAPKTDIVAGSTIDQAVNATFAALVYRTPDLYEKLQKYVNSGGKIALTEEFSQVYSLADGIRIWMLEMKQKSLLSLGNDSEEKRGLEAAEVNPESLAKECIQKSLLLLKFLPMSKSSKENCDKLETVDETDHLQPLDRRQRTSSVVEEHFQGSASPTEAATPAAGDRSPALEIQPKLLPSSGPCVAEVSTAEEPSPPSTPTRRPPFTRGRLRLLSFRSMEETRPVPTVKEKYPVLKDVMDFIKDQSLSHESVVKVLSLRKAQGQSILEVLRIIQYCTESLGQPHCFHPPYILFLLELLTCQKDFTNYFGHLEGCGADLHREIRDTYYQLVLFLVKAIKRFSSINDRSLLPALSCVQTALLHLLDMGWEPSDLAFFVDIQLPDLLMNMSQENISVHDSVISQWSEEDELADAKQNSEWMDECQDGMFEAWYEKIAQEDPEKQRKMHMFIARYCDLLNVDISCDGCDEIAPWHRYRCLQCSDMDLCKTCFLGGVKPEGHGDDHEMVNMEFTCDHCQGLIIGRRMNCNVCDDFDLCYGCYTAKKYSYGHLPTHSITAHPMVTIRISDRQRLIQPYIHNYSWLLFAALALYSAHLTSTEQVDGEQLDPQARTNAATLRSQCMQLVGDCLMKAHQGKGLKALALLGVLPDGDSTSENQALPVTVSFQASEEQADAGLLVPCNGKRAADTEVRPLDYKQKKKAGEDLSIVKDPSCQTQVSDAPASAHVPPGLPDAEHPEVSAQVLVEEKAITPNPEQVFAECSQKRILGLLAAMLPPIKSGPTVPLIDLEHVLPLMFQVVISNAGHLNETYHLTLGLLGQLIIRLQPAEVDAAVMKVLSAKHNLRVGLDWACSMAEILRSLNNAPLWRDVIATFTDHCIKQLPFQLKHTNIFTLLVLVGFPQVLCVGTRCVYMDNANEPHNVIILKHFTEKNRAVIVDVKTRKRKTVKDYQLVQKGGGQECGTSQSQLSQYSQHFAFIASHLLQTSMDSHCPEAVEATWVLSLALKGLYKTLKAHGFEETHATFLQTDLLKLLVKKCSKGTGFSKTWLLRDLEILSIMLYSSKKEINTLAEHGDLELDERGDQEEELDRPVSSPGEAEQKKLDPLENLDEPTRICFLMAHDALNAPLHILRAIYELQMKKTDSFFLEVQKRFDGDELTTDERIRSLAQRWQPSRSLRLEEQSAKAVDTDMIILPCLSRPARSDQATPESNPVTQKLISSTESELQQSYAKQRRSKSAALLHKELNCKSKRAIRDYLFRVNEATSVLYARHVLASLLAEWPGHVPVSEDILELSGPAHMTYILDMFMQLEEKHQWEKILQKVLQGCRENMLGTMALAACQFMEEPGMEVQVRESKHSYNNNTSFEDKVHIPGAIYLSIKFDPQRNTEEGCDELAMSSSSDFQQDRHNFSGSQQKWKDFELPGDTLYYRFTSDMSNTEWGYRFTVTAGHLGRFQTGFEILKQMLSEERVVPHLALGKIWEWLVGVACRQTGHQRLKAIHLLLRIVQCCSHSDLCDLGLLKPLWQLFTHMEYGLFEDVTQPGILLPLHRALTELFFVTENRAQELGLLQEYLLALTTEDHLLRCAAQALQNIAAISLAINYPNKATRLWNVEC |
Q8IYH5 | [
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] | ZZ-type zinc finger-containing protein 3 | Homo sapiens | Mammalia | Chordata | ZZZ3 | 903 | 1 | 1 | 9,606 | 9,606 | Histone H3 reader that is required for the ATAC complex-mediated maintenance of histone acetylation and gene activation (PubMed:30217978). Component of the ATAC complex, a complex with histone acetyltransferase activity on histones H3 and H4 (PubMed:19103755) | MAASRSTRVTRSTVGLNGLDESFCGRTLRNRSIAHPEEISSNSQVRSRSPKKRPEPVPIQKGNNNGRTTDLKQQSTRESWVSPRKRGLSSSEKDNIERQAIENCERRQTEPVSPVLKRIKRCLRSEAPNSSEEDSPIKSDKESVEQRSTVVDNDADFQGTKRACRCLILDDCEKREIKKVNVSEEGPLNSAVVEEITGYLAVNGVDDSDSAVINCDDCQPDGNTKQNSIGSYVLQEKSVAENGDTDTQTSMFLDSRKEDSYIDHKVPCTDSQVQVKLEDHKIVTACLPVEHVNQLTTEPATGPFSETQSSLRDSEEEVDVVGDSSASKEQCKENTNNELDTSLESMPASGEPEPSPVLDCVSAQMMSLSEPQEHRYTLRTSPRRAAPTRGSPTKNSSPYRENGQFEENNLSPNETNATVSDNVSQSPTNPGEISQNEKGICCDSQNNGSEGVSKPPSEARLNIGHLPSAKESASQHITEEEDDDPDVYYFESDHVALKHNKDYQRLLQTIAVLEAQRSQAVQDLESLGRHQREALKNPIGFVEKLQKKADIGLPYPQRVVQLPEIVWDQYTHSLGNFEREFKNRKRHTRRVKLVFDKVGLPARPKSPLDPKKDGESLSYSMLPLSDGPEGSSSRPQMIRGRLCDDTKPETFNQLWTVEEQKKLEQLLIKYPPEEVESRRWQKIADELGNRTAKQVASRVQKYFIKLTKAGIPVPGRTPNLYIYSKKSSTSRRQHPLNKHLFKPSTFMTSHEPPVYMDEDDDRSCFHSHMNTAVEDASDDESIPIMYRNLPEYKELLQFKKLKKQKLQQMQAESGFVQHVGFKCDNCGIEPIQGVRWHCQDCPPEMSLDFCDSCSDCLHETDIHKEDHQLEPIYRSETFLDRDYCVSQGTSYNYLDPNYFPANR |
Q6KAQ7 | [
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] | ZZ-type zinc finger-containing protein 3 | Mus musculus | Mammalia | Chordata | Zzz3 | 910 | 1 | 2 | 10,090 | 10,090 | Histone H3 reader that is required for the ATAC complex-mediated maintenance of histone acetylation and gene activation (By similarity). Component of the ATAC complex, a complex with histone acetyltransferase activity on histones H3 and H4 (By similarity) | MVGTCHSMAASRSTRVTRSTVGLNGLDESFCGRTLRNRSIAHPEEISSHSQVRSRSPKKRAEPVPTQKGTNNGRTSDVRQQSARDSWVSPRKRRLSSSEKDDLERQALESCERRQAEPAPPVFKNIKRCLRAEATNSSEEDSPVKPDKEPGEHRRIVVDHDADFQGAKRACRCLILDDCEKREVKKVNVSEEGPLNAAVVEEITGYLTVNGVDDSDSAVINCDDCQPDGNTKQNNPGSCVLQEESVAGDGDSETQTSVFCGSRKEDSCIDHFVPCTKSDVQVKLEDHKLVTACLPVERRNQLTAESASGPVSEIQSSLRDSEEEVDVVGDSSASKEQCNENSSNPLDTGSERMPVSGEPELSSILDCVSAQMTSLSEPQEHRYTLRTSPRRAALARSSPTKTTSPYRENGQLEETNLSPQETNTTVSDHVSESPTDPAEVPQDGKVLCCDSENYGSEGLSKPPSEARVNIGHLPSAKESASQHTAEEEDDDPDVYYFESDHVALKHNKDYQRLLQTIAVLEAQRSQAVQDLESLGKHQREALKNPIGFVEKLQKKADIGLPYPQRVVQLPEIMWDQYTNSLGNFEREFKHRKRHTRRVKLVFDKVGLPARPKSPLDPKKDGESLSYSMLPLSDGPEGSHNRPQMIRGRLCDDSKPETFNQLWTVEEQKKLEQLLLKYPPEEVESRRWQKIADELGNRTAKQVASRVQKYFIKLTKAGIPVPGRTPNLYIYSRKSSTSRRQHPLNKHLFKPSTFMTSHEPPVYMDEDDDRSCLHSHMSTAAEEASDEESIPIIYRSLPEYKELLQFKKLKKQKLQQMQAESGFVQHVGFKCDNCGVEPIQGVRWHCQDCPPEMSLDFCDSCSDCPHETDIHKEDHQLEPVYKSETFLDRDYCVSQGTSYSYLDPNYFPANR |
B0BLK0 | [
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] | RING finger protein Z | Allpahuayo mammarenavirus (isolate Rat/Peru/CLHP-2472/1997) | Ellioviricetes | Negarnaviricota | Z | 95 | 3 | 1 | 144,752 | 144,752 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGLRYSKEVRDRHGDKDIEGRVPMTLNLPQGLYGRFNCKSCWFVNKGLIACGDHYLCLGCLTRMLSRTDFCEICSKPLPKKIIFEDSPSAPPYEP |
A0PJ23 | [
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] | RING finger protein Z | Bear Canyon mammarenavirus (isolate Mouse/United States/AV A0070039/2000) | Ellioviricetes | Negarnaviricota | Z | 95 | 3 | 1 | 3,052,298 | 192,848 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGLRYSREVKQRYGEKELEGRIPITLDMPQTLYGRYNCKSCWFANKGLIKCSNHYLCLKCLTAMLSRSDYCGICGGILPKKLVFETTPSAPPYTP |
Q9G058 | [
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] | Uncharacterized protein Z | Bdellovibrio phage phiMH2K | Malgrandaviricetes | Phixviricota | ORFZ | 64 | 4 | 1 | 145,579 | 145,579 | null | MGQLGKIQRSTRQPIGLNGLFDPNNHSTRWWLRKHVHLRSLRNSDTSCKSRDKCSTFQSLQSYL |
B2C4J2 | [
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] | RING finger protein Z | Chapare mammarenavirus (isolate Human/Bolivia/810419/2003) | Ellioviricetes | Negarnaviricota | Z | 98 | 3 | 1 | 3,052,302 | 499,556 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNTKTKDRQYQSNSSQPTNTSAPVLLRRQAEPSLYGRHNCRCCWFADTNLVNCSNHYLCLKCLNTMLRRSNLCDICGEELPTTIIVPVEPSAPLPGQ |
B0BLK9 | [
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] | RING finger protein Z | Cupixi mammarenavirus (isolate Rat/Brasil/BeAn 119303/1970) | Ellioviricetes | Negarnaviricota | Z | 96 | 3 | 1 | 3,052,304 | 208,899 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNCRSKQESHPICPNTQTPEPTEAEFRRAAVNSLYGRYNCKCCWFADRNLINCSDHYLCLRCLNVMLRTSNLCNICWKPLPTRISVPTEPTAPSE |
Q6UY71 | [
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] | RING finger protein Z | Guanarito mammarenavirus (isolate Human/Venezuela/NH-95551/1990) | Ellioviricetes | Negarnaviricota | Z | 95 | 1 | 1 | 3,052,307 | 45,219 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNSKSKSNPSSSSESQKGAPTVTEFRRTAIHSLYGRYNCKCCWFADKNLIKCSDHYLCLRCLNVMLKNSDLCNICWEQLPTCITVPEEPSAPPE |
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] | RING finger protein Z | Ippy mammarenavirus (isolate Rat/Central African Republic/Dak An B 188 d/1970) | Ellioviricetes | Negarnaviricota | Z | 101 | 3 | 1 | 3,052,308 | 55,096 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGQNQSRDKQKAIQNQPKDTGNRADIIPDATGMGPEFCKSCWFERRSLVACNNHYLCMNCLTLLLSVSERCPICKLPLPQKLKLTSSPSAPPSPSPPPYSP |
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] | RING finger protein Z | Junin mammarenavirus | Ellioviricetes | Negarnaviricota | Z | 94 | 1 | 1 | 2,169,991 | 2,169,991 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNCNGASKSNQPDSSRVTQPAAEFRRVAHSSLYGRYNCKCCWFADTNLITCNDHYLCLRCHQVMLRNSDLCNICWKPLPTTITVPVEPTAPPP |
O73557 | [
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] | RING finger protein Z | Lassa virus (strain Mouse/Sierra Leone/Josiah/1976) | Ellioviricetes | Negarnaviricota | Z | 99 | 1 | 4 | 11,622 | 11,622 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNKQAKAPESKDSPRASLIPDATHLGPQFCKSCWFENKGLVECNNHYLCLNCLTLLLSVSNRCPICKMPLPTKLRPSAAPTAPPTGAADSIRPPPYSP |
A9JR44 | [
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] | RING finger protein Z | Latino mammarenavirus (isolate Rat/Bolivia/MARU 1924/1965) | Ellioviricetes | Negarnaviricota | Z | 91 | 3 | 1 | 3,052,311 | 45,221 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGSKQSAPPKPLQLPQPRVSLLREAKPSLYGRYNCKCCWFQDKNLVECSDHYLCLKCISSMLKRGKNCEICGKAIPTYIEVGITPTAPQLN |
P18541 | [
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] | RING finger protein Z | Lymphocytic choriomeningitis virus (strain Armstrong) | Ellioviricetes | Negarnaviricota | Z | 90 | 1 | 3 | 11,624 | 11,624 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host EIF4E (PubMed:10708446, PubMed:11575918) | MGQGKSREEKGTNSTNRAEILPDTTYLGPLSCKSCWQKFDSLVRCHDHYLCRHCLNLLLSVSDRCPLCKYPLPTRLKISTAPSSPPPYEE |
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] | RING finger protein Z (Fragment) | Lymphocytic choriomeningitis virus (strain Pasteur) | Ellioviricetes | Negarnaviricota | Z | 51 | 3 | 1 | 11,625 | 11,625 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z (By similarity) | PDTTYLGPLNCKSCWQKFDSLVRCHDHYLCRHCLNLLLTSSDRCPLCKYPL |
P19325 | [
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] | RING finger protein Z (Fragment) | Lymphocytic choriomeningitis virus (strain Traub) | Ellioviricetes | Negarnaviricota | Z | 72 | 3 | 3 | 11,626 | 11,626 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z (By similarity) | MGQSKSKEEKGISGTSRAEILPDTTYLGPLNCKSCWQKFDSFSKCHDHYLCRHCLNLLLTSSDRCPLCKYPL |
Q6IUF9 | [
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] | RING finger protein Z | Machupo virus | Ellioviricetes | Negarnaviricota | Z | 94 | 1 | 1 | 3,052,317 | 11,628 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNCNKPPKRPPNTQTSAAQPSAEFRRTALPSLYGRYNCKCCWFADTNLITCNDHYLCLRCHQTMLRNSELCHICWKPLPTSITVPVEPSAPPP |
Q27YE6 | [
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] | RING finger protein Z | Mobala mammarenavirus (isolate Rat/Central African Republic/Acar 3080/1983) | Ellioviricetes | Negarnaviricota | Z | 99 | 3 | 1 | 3,052,325 | 55,097 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGQKPSKPKAPPTTYESPRSSLTPDATGFGPEFCKSCWFERKGLIKCQNHYLCMTCLTLLLTVSNRCPVCKYPLPTKLRLEKSPTAPPPEATNPPPYSP |
B0BLK7 | [
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] | RING finger protein Z | Oliveros mammarenavirus (isolate Mouse/Argentina/RIID 3229/1990) | Ellioviricetes | Negarnaviricota | Z | 99 | 3 | 1 | 3,052,322 | 42,764 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGSKSSKSSGFENVPSLGLSHTNQPRVSLIREARPSLYGRYNCKCCWFQNKNLVECSDHYLCLKCISSMLRRGQNCEICGKPIPTHIAVTTAPTAPPEP |
B2MW50 | [
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] | RING finger protein Z | Parana mammarenavirus (isolate Rat/Paraguay/12056/1965) | Ellioviricetes | Negarnaviricota | Z | 95 | 3 | 1 | 3,052,323 | 2,169,994 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGLRYSKAVKDKYGDREIEGRATMTLNLPQGLYGRFNCKRCWFATKGLIACSDHYLCLNCLTIMLSDGNFCEVCGKTLPKKIVFEESPSAPPYDG |
Q6RSS3 | [
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] | RING finger protein Z | Pirital mammarenavirus (isolate Rat/Venezuela/VAV-488/1995) | Ellioviricetes | Negarnaviricota | Z | 95 | 3 | 1 | 3,052,324 | 49,891 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGLRYSKEVRERHGDKDLEGRVPMTLNLPQGLYGRFNCKSCWFANRGLIACSDHYLCLNCLTRLRSQSQFCGICGKPLPTKIRFEESPSAPPYEP |
Q6UY62 | [
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] | RING finger protein Z | Sabia mammarenavirus (isolate Human/Brasil/SPH114202/1990) | Ellioviricetes | Negarnaviricota | Z | 100 | 1 | 1 | 3,052,299 | 2,169,992 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNSKSKSKLSANQYEQQTVNSTKQVAILKRQAEPSLYGRHNCRCCWFANTNLIKCSDHYICLKCLNIMLGKSSFCDICGEELPTSIVVPIEPSAPPPED |
P08105 | [
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] | Putative uncharacterized protein Z | Ovis aries | Mammalia | Chordata | null | 79 | 4 | 1 | 9,940 | 9,940 | null | MSSSLEITSFYSFIWTPHIGPLLFGIGLWFSMFKEPSHFCPCQHPHFVEVVIPCDSLSRSLRLRVIVLFLAIFFPLLNI |
Q88470 | [
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] | RING finger protein Z | Tacaribe virus (strain Franze-Fernandez) | Ellioviricetes | Negarnaviricota | Z | 95 | 1 | 3 | 928,313 | 928,313 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGNCNRTQKPSSSSNNLEKPPQAAEFRRTAEPSLYGRYNCKCCWFADKNLITCSDHYLCLRCHQIMLRNSELCNICWKPLPTSIRVPLEASAPDL |
A9JR22 | [
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] | RING finger protein Z | Tamiami mammarenavirus (isolate Rat/United States/W 10777/1964) | Ellioviricetes | Negarnaviricota | Z | 95 | 3 | 1 | 3,052,329 | 45,223 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGLRYSKEVRDRHGDKDPEGRIPITQTMPQTLYGRYNCKSCWFANKGLIKCSNHYICLRCLTSMLNRTDYCEICGEVLPKRLTFETTPTAPPYTP |
B2ZDY1 | [
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] | RING finger protein Z | Whitewater Arroyo mammarenavirus (isolate Rat/United States/AV 9310135/1995) | Ellioviricetes | Negarnaviricota | Z | 95 | 3 | 1 | 3,052,331 | 46,919 | Plays a crucial role in virion assembly and budding. Expressed late in the virus life cycle, it acts as an inhibitor of viral transcription and RNA synthesis by interacting with the viral polymerase L. Presumably recruits the NP encapsidated genome to cellular membranes at budding sites via direct interaction with NP. Plays critical roles in the final steps of viral release by interacting with host TSG101, a member of the vacuolar protein-sorting pathway and using other cellular host proteins involved in vesicle formation pathway. The budding of the virus progeny occurs after association of protein Z with the viral glycoprotein complex SSP-GP1-GP2 at the cell periphery, step that requires myristoylation of protein Z. Also selectively represses protein production by associating with host eIF4E | MGLRYSKDVKDRYGDREPEGRIPITLNMPQSLYGRYNCKSCWFANKGLLKCSNHYLCLKCLTLMLRRSDYCGICGEVLPKKLVFENSPSAPPYEA |