protein_name
stringlengths 6
11
| species
stringclasses 299
values | sequence
stringlengths 5
4.97k
| annotation
stringlengths 5
2.1k
⌀ |
|---|---|---|---|
IAA2_HORVU | Hordeum vulgare | MGAMWMKSMLLVLLLCMLMVTPMTGARSDNSGPWMWCDPEMGHKVSPLTRCRALVKLECVGNRVPEDVLRDCCQEVANISNEWCRCGDLGSMLRSVYAALGVGGGPEEVFPGCQKDVMKLLVAGVPALCNVPIPNEAAGTRGVCYWSASTDT | Could be involved in insect defense mechanisms. Inhibits insect-type alpha-amylase.
Subcellular locations: Secreted
Endosperm. |
IAA2_ORYSJ | Oryza sativa subsp. japonica | MAWRRGFGREEEDAAAAGESGLELCLGLPAYFSSSSSSKPSEGSTAAPAFALRSNGTNASKPSGAAAAAPVVGWPPVRSFRRNLASSSSSSSKQAPPPPSSSPQNGDKASKDGGAEKGMFVKINMDGVPIGRKVDLAAYGGYAQLSAAVDKLFRGLLAAQSAAADGEADAAAAGEMVGGGEYTLVYEDDEGDRMLVGDVPWQMFIATAKRLRVLKSSDLPPPSLMRAAGSRKRAAADS | Aux/IAA proteins are short-lived transcriptional factors that function as repressors of early auxin response genes at low auxin concentrations.
Subcellular locations: Nucleus
Highly expressed in flowers. |
IAA2_WHEAT | Triticum aestivum | MWMKTVFWGLLVFMLVATTMAVEYGARSHNSGPWSWCNPATGYKVSALTGCRAMVKLQCVGSQVPEAVLRDCCQQLADINNEWCRCGDLSSMLRSVYQELGVREGKEVLPGCRKEVMKLTAASVPEVCKVPIPNPSGDRAGVCYGDWAAYPDV | Alpha-amylase inhibitor.
Subcellular locations: Secreted
Endosperm. |
IAA30_ORYSJ | Oryza sativa subsp. japonica | MAADLAFEATELRLGLPGGGGDGDAAAAAARSSSGKRGFAETIDLKLKLEPAAAAVDDDDDKEEAAADDREKKVDIVGADNDDASPPAAAAAGGMKRSPSQSSVVTAAADPEKPRAPKAQVVGWPPVRSYRKNILAVQADKGKDAADGGGDKSGAGAAAAAFVKVSMDGAPYLRKVDLKMYKSYLELSKALEKMFSSFTIGNCGSHGVNGMNESKIADLLNGSEYVPTYEDKDGDWMLVGDVPWEMFVESCKRLRIMKGSEAIGLAPRAMEKCKNRS | Aux/IAA proteins are short-lived transcriptional factors that function as repressors of early auxin response genes at low auxin concentrations.
Subcellular locations: Nucleus
Highly expressed in etiolated seedlings. Expressed in roots and flowers. |
IAA31_ORYSJ | Oryza sativa subsp. japonica | MENLKATELRLGLPGTEEEAAPPPSTPRAGSKRALAGEPDQAKIKPAAAAKAQVVGWPPVRSYRKSCLQPTTTTTKSKPPPAAAAAETQQKEDVAGAGGLFVKVSMDGAPYLRKIDLKVYKGYRELREALEAMFLCFSGGAAADAAVNPSDFAVTYEDKDGDLMLVGDVPFEMFISTCKRLRIMKGSEARGLGATRG | Aux/IAA proteins are short-lived transcriptional factors that function as repressors of early auxin response genes at low auxin concentrations.
Subcellular locations: Nucleus
Highly expressed in etiolated seedlings. Expressed in roots. |
IAA3_ORYSJ | Oryza sativa subsp. japonica | MSPPLELDYIGLSPPPPPPSSSSAAAARADDVDLKGTELRLGLPGSESPDRRPAAIAAAAATATTLELLPAKGAKRVFPDEAALTPPTAAAGKGKAAREGEEVGAEEEDKKVAAPPQPAAKAQVVGWPPIRSYRKNTMATNQIKSNKEDVDAKQGQGFLYVKVSMDGAPYLRKVDLKTYKNYKDMSLGLEKMFIGFSTGKEGAENQKDGEYVLTYEDKDGDWMLVGDVPWEMFTDSCRRLRIMKGSDAIGLAPRAGEKSKNRN | Aux/IAA proteins are short-lived transcriptional factors that function as repressors of early auxin response genes at low auxin concentrations.
Subcellular locations: Nucleus
Highly expressed in flowers. Expressed in roots and shoots. |
IAA3_WHEAT | Triticum aestivum | SGPWMCYPGYAFKVPALPGCRPVLLLQCNGSQVPEAVLRDCCQQ | Alpha-amylase inhibitor.
Subcellular locations: Secreted
Endosperm. |
IAMT1_ORYSJ | Oryza sativa subsp. japonica | MTMAMASMKGENVTVSAAAAPRMKKLASMLCMKGGNGDGSYLNNSQAQALHARRMLHFLEETLDAMMERSSSDKLFTAADLGCSCGSNSLFIVDVIVRRVSEAYESRGRDAPEFQVFFSDLPSNDFNTLFQLLPPLLAPVAGSLEECLAAGEGAATATRPYHAAGVPGTFYGRLFPGESIDVFTSTFSLHWLSQVPEEVGDSASPAYNGGRVFVHRATEAVAAAYKRQFQADLARFLRSRAREMKRGGAMFLACLGRSSGDPADQGGAGLLFGTHFQDAWDDLVQEGVVEGEKRDSFNIPVYAPSLQEFRDVVRADGAFAIDRLELVRGGSPLVVDRPDDAAEVGRAMANSCKAVAGVLVDAHIGERRGAQLFERLERRAARHARELVEKMHFFHVVCSLSLAP | Catalyzes the methylation of the free carboxyl end of the plant hormone indole-3-acetic acid (IAA). Converts IAA to IAA methyl ester (MeIAA). Regulates IAA activities by IAA methylation. Methylation of IAA plays an important role in regulating plant development and auxin homeostasis. MeIAA seems to be an inactive form of IAA.
Expressed in roots and panicles. |
ICI1_CANLI | Canavalia lineata | STRKTSWPELVGVTAEEAEKIKEEMSGVEIQVVPPGSFVTADYKPQRVRLYVDESNKVTRTPGIG | Inhibits subtilisin-type microbial serine proteases including proteinase K, subtilisin BPN', subtilisin Carlsberg, subtilisin E, A.oryzae protease and S.griseus alkaline protease. Weakly inhibits pronase E. Does not inhibit trypsin or chymotrypsin. |
ICI1_PHAAN | Phaseolus angularis | QEQGTNPSQEQNVPLPRNYKQALETNTPTKTSWPELVGVTAEQAETKIKEEMVDVQIQVSPHDSFVTADYNPKRVRLYVDESNKVTRTPSIG | Inhibitor of subtilisin. |
ICI1_SOLLC | Solanum lycopersicum | MESKFAHIIVFFLLATSFETLMARKEIDGPEVIELLKEFDSNLMCEGKQMWPELIGVPTKLAKEIIEKENPSITNIPILLSGSPITLDYLCDRVRLFDNILGFVVQMPVVT | Subcellular locations: Secreted |
ICI1_SOLPE | Solanum peruvianum | MEAKFAHIILFFLLAFSFETLMARKESDGPEVIKLLKEFESDSRCKGKQFWPELIGVPALYAKGIIEKENPSITNIPILLNGSPVTKDFRCDRVRLFVNILGDVVQIPRVT | Subcellular locations: Secreted |
ICI1_SOLTU | Solanum tuberosum | MELKFAHIIVFFLLATSFETLMARKESDGPEVIQLLKEFQCKGKLRWPELIGVPTKLAKGIIEKENSLISNVHILLNGSPVTLDIRCDRVRLFDNILGYVVDIPVVG | null |
ICI2_CANLI | Canavalia lineata | NDVDVVMDASSKPIFPGGEYYIMPAIWGPPGGGVRLAKTRNSDCPVTVLQDYGEVIFGQPVKFTLPGRGSGLIITNTPVEEFIKKPECASSSKWSVFVDDEIEKACVGIGGHEDHPGEQVFSGTFTIQKSRTPYNSYKLVFCESDSSTCSDIGRYDNNEGGRRLILTHHNPFQVVFMDASTFDGTIRSDG | Inhibits subtilisin-type microbial serine proteases incuding proteinase K, subtilisin BPN', subtilisin Carlsberg and subtilisin E in a non-stoichiometric manner. Weakly inhibits A.oryzae protease and some metalloproteases including pronase E. Does not inhibit trypsin, chymotrypsin, S.griseus alkaline protease or A.lyticus lysyl endopeptidase. CLSI-II has a wider inhibitory specificity than CLSI-III.
Subcellular locations: Secreted |
ICI2_HORVU | Hordeum vulgare | MSSVEKKPEGVNTGAGDRHNLKTEWPELVGKSVEEAKKVILQDKPEAQIIVLPVGTIVTMEYRIDRVRLFVDKLDNIAQVPRVG | Inhibits both subtilisin and chymotrypsin. |
ICI3_HORVU | Hordeum vulgare | DCLCDCQNQKTEWPELVEKSVEEAKKVILQDKPEAQIIVLPVGTIVTMEYRIDRVRLFVDRLDNIAQVPRVG | Inhibits both subtilisin and chymotrypsin. |
ICIA_HORVU | Hordeum vulgare | MSSMEGSVLKYPEPTEGSIGASSAKTSWPEVVGMSAEKAKEIILRDKPNAQVEVIPVDAMVHLNFDPNRVFVLVAVARTPTVG | Inhibits both subtilisin and chymotrypsin. |
ICIA_SOLTU | Solanum tuberosum | KEFECDGKLQWPELIGVPTKLAKEIIEKQNSLISNVHILLNGSPVTMDFRCNRVRLFDDILGSVVQIPRVA | Inhibits both chymotrypsin and trypsin. |
ICIB_HORVU | Hordeum vulgare | MRSMEGSVPKYPEPTEGSIGASGAKRSWPEVVGMSAEKAKEIILRDKPDAQIEVIPVDAMVPLDFNPNRIFILVAVARTPTVG | Inhibits both subtilisin and chymotrypsin. |
ICIC_HORVU | Hordeum vulgare | YPEPTEGSIGASGAKTSWPEVVGMSAEKAKEIILRDKPNAQIEVIPVDAMVPLNFNPNRVFVLVHKATTVAZVSRVG | Inhibits both subtilisin and chymotrypsin. |
ICID_SOLTU | Solanum tuberosum | MESKFAHIIVFFLLATSFETLLARKESDGPEVIELQKEFECNGKQRWPELIGVPTKLAKGIIEKENSLITNVQILLNGSPVTMDYRCNRVRLFDNILGDVVQIPRVA | Inhibits both chymotrypsin and trypsin. |
ICIS_VICFA | Vicia faba | RTSWPELVGVSAEEARKIKEEMPEAEIQVVPQDSFVTADYKFQRVRLYVDESNKVVRAAPIG | Inhibits subtilisin and more weakly elastase. |
ICIW2_WHEAT | Triticum aestivum | TSIYTCYEGVGLPVDPLQGCHYYVTSQTCGFVPLLPIEVMKDRCCRELAAISSNCRCEGLRVFIDRAFPPSQSQGGGPPQPPLAPRCPTEVKRDFARTLALPGQCNLPTIHGGPYCVFP | Inhibits bovine, insect and wheat chymotrypsins. Inhibits bovine chymotrypsin with Ki of 0.6 nM. Does not inhibit human or wheat alpha-amylases, bovine pancreatic trypsin, or trypsin-like activity isolated from wheat.
Subcellular locations: Secreted |
ICIW_WHEAT | Triticum aestivum | MSSVVKKPLGGNTDTGDHHNQKTEWPELVGKSVEEAKKVILQDKSEAQIVVLPVGTIVTMEYRIDRVRLFVDSLDKIAQVPRVG | Inhibits B.lichenoformis subtilisin, B.subtilis subtilisin, bovine pancreatic alpha-chymotrypsin and porcine alpha-chymotrypsin with Ki of 3.92 nM, 5.70 nM, 7.24 nM and 9.35 nM respectively. B.lichenoformis subtilisin is inhibited with a molar ratio of 1:0.87. Also inhibits chymotrypsin-like activities from the digestive tracts of the insect larvae T.molitor, P.interpunctella and H.armigera. Does not inhibit bovine pancreatic trypsin, porcine pancreatic elastase, or human leukocyte elastase.
Subcellular locations: Secreted |
ICMT_ORYSI | Oryza sativa subsp. indica | MAARAQAWLFAAALVIFHGSEYVLAAAFHGRRNVTATSLLISKQYVLAMSFAMLEHLTEALLFPELKEYWFVSYVGLVMVIIGEVIRKLAVVTAGRSFTHVIRIHYEDQHKLITHGVYRLMRHPGYSGFLIWAVGTQVMLCNPLSTVAFTLVLWRFFSKRIPYEEFFLRQFFGREYEEYAQKVHSGLPFIE | Catalyzes the post-translational methylation of isoprenylated C-terminal cysteine residues. Carboxyl methylation is a reversible and potentially regulated step in the post-translational modification of prenylated proteins (By similarity).
Subcellular locations: Endoplasmic reticulum membrane |
ICMT_ORYSJ | Oryza sativa subsp. japonica | MAARAQAWLFAAALVIFHGSEYVLAAAFHGRRNVTATSLLISKQYVLAMSFAMLEHLTEALLFPELKEYWFVSYVGLVMVIIGEVIRKLAVVTAGRSFTHVIRIHYEDQHKLITHGVYRLMRHPGYSGFLIWAVGTQVMLCNPLSTVAFTLVLWRFFSKRIPYEEFFLRQFFGREYEEYAQKVHSGLPFIE | Catalyzes the post-translational methylation of isoprenylated C-terminal cysteine residues. Carboxyl methylation is a reversible and potentially regulated step in the post-translational modification of prenylated proteins (By similarity).
Subcellular locations: Endoplasmic reticulum membrane |
IF1C_HORVU | Hordeum vulgare | MTEKKNRREKKNPREAKVTFEGLVTEALPNGMFRVRLENDTIILGYISGKIRSSSIRILMGDRVKIEVSRYDSSKGRIIYRLPHKDSKRIEDSKDSEDLKDSEDLKDTKDSKD | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre-initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initiation complex.
Subcellular locations: Plastid, Chloroplast |
IF4G1_ORYSJ | Oryza sativa subsp. japonica | MEKDHQPVISLRPGGGGGGPRPGRLFSPAFAAAASGSGDLLRSHVGGASKIGDPNFEVRERVRYTRDQLLELREIVDIPEAILRINQEIDIELHGEDQIWGRPESDVQVQTQTQAQPHNRYGETDNRDWRARTVQPPAANEEKSWDNIREAKAAHASSGRQQEQVNRQDQLNHQFASKAQVGPTPALIKAEVPWSARRGNLSEKDRVLKTVKGILNKLTPEKFDLLKGQLMESGITTADILKDVISLIFEKAVFEPTFCPMYAQLCSDLNEKLPSFPSEEPGGKEITFKRVLLNNCQEAFEGAESLRAEIAKLTGPDQEMERRDKERIVKLRTLGNIRLIGELLKQKMVPEKIVHHIVQELLGSGPDKKACPEEENVEAICQFFNTIGKQLDENPKSRRINDTYFIQMKELTTNLQLAPRLRFMVRDVVDLRSNNWVPRREEIKAKTISEIHDEAMKTLGLRPGATGLTRNGRNAPGGPLSPGGFPMNRPGTGGMMPGMPGTPGMPGSRKMPGMPGLDNDNWEVPRSKSMPRGDSLRNQGPLLNKPSSINKPSSINSRLLPHGSGALIGKSALLGSGGPPSRPSSLMASLTHTPAQTAPSPKPVSAAPAVVPVTDKAAGSSHEMPAAVQKKTVSLLEEYFGIRILDEAQQCIEELQCPEYYSEIVKEAINLALDKGPNFIDPLVRLLEHLHAKKIFKTEDLKTGCLLYAALLEDIGIDLPLAPALFGEVVARLSLSCGLSFEVVEEILKAVEDTYFRKGIFDAVMKTMGGNSSGQAILSSHAVVIDACNKLLK | Plays a role in the accumulation of a sobemovirus (RYMV) during viral infection. |
IF4G1_WHEAT | Triticum aestivum | MTTDQPVISLRPGGGGGGPRGGRLFAPAFAVAASGSGDFLRPHGGGASGVSRIGDLHSESRERVRYSRDQLLDLRKITDVTEQILRLQQEIEAELNGDDQSWVRNDSNVQLQTQAQPQVQAQNRFTETDNRDWRARTEKPPAPAVQEEKSWDNIREVKEQYNASGRQQEQFNRQDQSSSQKAQVGPPPALIKADVPWSARRGNLSEKDRVLKTVKGILNKLTPEKFDLLKGQLLDSGITTADILKDVISLIFEKAVFEPTFCPMYAQLCSELNDNLPTFPSEEPGGKEITFKRVLLNNCQEAFEGADSLRVEIASLTGPDQEMEKRDKERIFKLRTLGNIRLIGELLKQKMVPEKIVHHIVKELLGSDKKACPDEEHVEAICQFFNTIGKQLDENPKSRRINDTYFVQIRELVANPQLTPRSKFMVRDLIDLRSNNWVPRRAEIKAKTISEIHTEAEKNLGLRPGATANMRNGRNAPGGPLSPGGFSVNRPGTGGMMPGMPGSRKMPGMPGLDNDNWEVQRSRSMPRGDPLRNQGPLINKVPSINKPSPINPRLLPQGTGALIGKSALLGTGGPPSRPSSLTASPTPLPAQTTASPKPSSATPASVPIPDKAASSAKVIPAGLQKKTASLLEEYFGIRILDEAQQCIEELQSPDYHPEIVKEAINLALDKGASFVDPLVKLLEHLYTKKTFKTEDLENGCLLYGSLLEDIGIDLPKAPTQFGEVVARLILSCGLRFEAAEGILKAMEDTFFRKAIFTSVTKTLGADPAGQAILSSHAAVVDACNSLSI | null |
ILVB1_ORYSJ | Oryza sativa subsp. japonica | MATTAAAAAAALSAAATAKTGRKNHQRHHVLPARGRVGAAAVRCSAVSPVTPPSPAPPATPLRPWGPAEPRKGADILVEALERCGVSDVFAYPGGASMEIHQALTRSPVITNHLFRHEQGEAFAASGYARASGRVGVCVATSGPGATNLVSALADALLDSVPMVAITGQVPRRMIGTDAFQETPIVEVTRSITKHNYLVLDVEDIPRVIQEAFFLASSGRPGPVLVDIPKDIQQQMAVPVWDTSMNLPGYIARLPKPPATELLEQVLRLVGESRRPILYVGGGCSASGDELRWFVELTGIPVTTTLMGLGNFPSDDPLSLRMLGMHGTVYANYAVDKADLLLAFGVRFDDRVTGKIEAFASRAKIVHIDIDPAEIGKNKQPHVSICADVKLALQGLNALLQQSTTKTSSDFSAWHNELDQQKREFPLGYKTFGEEIPPQYAIQVLDELTKGEAIIATGVGQHQMWAAQYYTYKRPRQWLSSAGLGAMGFGLPAAAGASVANPGVTVVDIDGDGSFLMNIQELALIRIENLPVKVMVLNNQHLGMVVQWEDRFYKANRAHTYLGNPECESEIYPDFVTIAKGFNIPAVRVTKKSEVRAAIKKMLETPGPYLLDIIVPHQEHVLPMIPSGGAFKDMILDGDGRTVY | Subcellular locations: Plastid, Chloroplast |
ILVB2_MAIZE | Zea mays | MATAATAAAALTGATTATPKSRRRAHHLATRRALAAPIRCSALSRATPTAPPATPLRPWGPNEPRKGSDILVEALERCGVRDVFAYPGGASMEIHQALTRSPVIANHLFRHEQGEAFAASAYARSSGRVGVCIATSGPGATNLVSALADALLDSVPMVAITGQVPRRMIGTDAFQETPIVEVTRSITKHNYLVLDVDDIPRVVQEAFFLASSGRPGPVLVDIPKDIQQQMAVPAWDTPMSLPGYIARLPKPPATEFLEQVLRLVGESRRPVLYVGGGCAASGEELCRFVELTGIPVTTTLMGLGNFPSDDPLSLRMLGMHGTVYANYAVDKADLLLAFGVRFDDRVTGKIEAFAGRAKIVHIDIDPAEIGKNKQPHVSICADVKLALQGMNTLLEGSTSKKSFDFGSWHDELDQQKREFPLGYKIFNEEIQPQYAIQVLDELTKGEAIIATGVGQHQMWAAQYYTYKRPRQWLSSAGLGAMGFGLPAAAGAAVANPGVTVVDIDGDGSFLMNIQELAMIRIENLPVKVFVLNNQHLGMVVQWEDRFYKANRAHTFLGNPENESEIYPDFVAIAKGFNIPAVRVTKKSEVHAAIKKMLEAPGPYLLDIIVPHQEHVLPMIPSGGAFKDMILDGDGRTVY | Subcellular locations: Plastid, Chloroplast |
ILVB2_ORYSJ | Oryza sativa subsp. japonica | MAAAAAAASLSVSDAAAKLPKPGGQVQRRRDRDRPRVDAAACTRDSRRPTRERCSTTVSLAATATATTATPVRAPVRTRAPMGQRKGADIVVEALERCGVRDVFEYPGGASMEIHQALTRSPVIRNHLLRHEQGEAFAASGYARSSGRPGVCVATSGPGATNLVSALADAHLDSVPLVAITGQAPRRMIGTDAFQETPIVEFTRSITKHNYLILDVDDIPRVINEAFFLASTGRPGPVLVDIPKDIQQQMAVPSWDAPMRLPGYISRLPKPPAANLLDEVIRLVGDAERPVLYVGGGCSASGYELRRFVELTGIPVTTTLMGIGNFPSDDPLSLRMLGMHGTVYANYAVDNADLLLALGVRFDDRVTGKVEAFASRAKIVHVDIDPSELGKNKQPHVSICADVKLALQGMNAMLEEQSAAAARKNLDFSAWRSELEKKKVEFPLGYRTFGEEIPPQYAIQVLDEVTNGEAIVATGVGQHQMWATQHYTYRRPRQWLSSAGLGAMGFGLPAAAGAAVANPGATVVDIDGDGSLLMNIQELAMVRVEDLPVKVMVLNNQHLGMVVQWEDRFYDANRAHTYLGNPAANGGGEVYPDFVTIAGGFGIPAARVTRKGEVRAAVEEMMAAPGPYLLDVVVPHQEHVLPMIPSNGAFKDIIVDGDGRSSY | Subcellular locations: Plastid, Chloroplast |
IMAP2_ORYSJ | Oryza sativa subsp. japonica | MADDSASPSPSSASPLQHHREALKSSVRNTAASRRREQAIAIGKERREALIRAKRVCRAPISGSDEAEMEEGDMVVDEEKACLEAKTAHAVEELKSALSIQGKGVQKKKIEALRDLRRLLSQPEVPLVDTAIKAGAVPLLVQYLSFGSSDEQLLEAAWCLTNIAAGEPEETKSLLPALPLLIAHLGEKSSTLVAEQCAWAIGNVAGEGAELRSTLLAQGALRPLTRLMFSSKGSTARTAAWAMSNLIKGPDPKAANELITIDGVLNAIIASLEKEDEELATEVAWVVVYLSALSDRGISLIVRSSVPQLLIGRLFSSENLQLLIPVLRGLGNLIAADDYMVDSVLTVGHNIIDQALSGLIKCLKSDNRVLRKESSWALSNIAAGSFEHKKLIFASEATPVLIRLVTSMQFDIRREAAYTLGNLCVVPTGNCELPKIIVEHLVAIVDGGALPGFIHLVRSADVDTAGLGLQFLELVMRGYPNKQGPKLVEMEDGIEAMERFQFHENEQMRNMANGLVDEYFGEDYGLDE | Binds specifically and directly to substrates containing either a simple or bipartite NLS motif. Promotes docking of import substrates to the nuclear envelope.
Subcellular locations: Cytoplasm, Perinuclear region
Expressed in root, callus, and etiolated leaf. Low expression in green leaf. |
IMA_SOLLC | Solanum lycopersicum | MSLRPNSRTEARRSRYKVAVDAEEGRRRREDNMVEIRKNKREENLLKKRREGLLQAQQFPSTAAVSHLDKKLETLPELIAGVWSDDSSLQLECTTQFRKLLSIERNPPIEEVIQSGVVPRFVEFLARDDYPQLQFEAAWALTNIASGTSENTKVVIDYGSVPIFIRLLSSPSDDVREQAVWALGNIAGDSPKYRDLVLGHGALVALLAQFNEQAKLSMLRNATWTLSNFCRGKPQPLFEQTKAALPTLGRLIHSNDEEVLTDACWALSYLSDGTNDKIQAVIEAGVCSRLVELLLHSSPSVLIPALRTVGNIVTGDDIQTQVMIDHHALPCLVNLLTQNYKKSIKKEACWTISNITAGNRNQIQIVIEAGIIAPLVYLLQNAEFEIKKEAAWAISNATSGGNHDQIKFLVSQGCIKPLCDLLVCPDPRIVTVCLEGLENILKIGEADKDLGNTEGVNVYAQLIDEAEGLEKIENLQSHDNTEIYEKAVKILETYWLEEEDVPVSLNEDQFEFGGADISLPSGGFNFS | Binds specifically and directly to substrates containing either a simple or bipartite NLS motif. Promotes docking of import substrates to the nuclear envelope. Seems to act as a cytosolic receptor for both simple and bipartite NLS motifs (By similarity).
Subcellular locations: Cytoplasm |
IPI1_ORYSJ | Oryza sativa subsp. japonica | MGAEEEEEPASAVGREGGGGGGGARAAGAGAGGDTADDDDSGESAAAVVPCSICLDAVVAGGGDRSTARLQCGHEFHLDCIGSAFNAKGVMQCPNCRQIERGNWLYANGSRPSQDVSNDDWGHDEDFYDANQPETSRSVFLPFRFQWCPIGRLAQLPSVFDEGESAPPVTFHDFMGQNFTSEHLPVSAPGATPPGPYIAYFQPLQSSASSSSSHVTERTMDGTTYHDHWNPLPGPSDGRPLATVHPIDFHHNHWTHLPNSYSQPNSNNGVAEQMAIPVVPMRVGGLDSDSQQRGSLPSVYGNGSGSRSRIPSVPPMAPQFMRPHGNINEQYQQNSSSLYAAPQRRTAVQAVQDSMNFTLFPQAPTGPNSMETEDAGGNQFYAWERDRFAPYPLMPVDSEANWWGSTPQSHGVTDHSAAPGRRLFGQWIGAGRSPPPPPPPPADNSSYRQMHIPRM | Functions as an E3 ligase that promotes polyubiquitination of SPL14/IPA1 for subsequent proteasomal degradation . Regulates plant architecture by modulating SPL14/IPA1 abundance . Promotes the degradation of SPL14/IPA1 in panicles, while it stabilizes SPL14/IPA1 in shoot apices . Ubiquitinates the SPL14/IPA1-mediated complex with 'Lys-48'-linked polyubiquitin in panicles and 'Lys-63'-linked polyubiquitin chains in the shoot apex .
Subcellular locations: Nucleus |
IRO2_ORYSI | Oryza sativa subsp. indica | MEQLFVDDPAFASSMSSLEADIFSGAGQLPSSPWLDLDLDDDVQDLSMAPTTANAVSSGYGSGGSGSHRKLSHNAYERDRRKQLNELYSSLRALLPDADHTKKLSIPTTVSRVLKYIPELQKQVENLERKKKELTTTSTTNCKPGVLGSQLMSEGMAPIVSATCINDMEIMVQVSLLSNVAGSVLPLSKCIKVLENEGLHFISSSTSSGFGNRTFYSIHLQRSEGTINEECPAFCERLEKVVRNKAKL | Transcription activator that binds to the DNA motif 5'-CACGTGG-3' in the promoter of iron (Fe) deficiency-inducible genes as well as of genes involved in iron homeostasis, thus contributing to basal tolerance to iron deficiency, iron uptake from soil and iron transport, particularly during seed maturation and germination. Promotes the accumulation of mugineic acid family phytosiderophores (MAs). Required for ethylene-mediated signaling during iron deficiency responses. Improves growth and yield, especially in calcareous soil with low iron availability. Promotes iron concentration in shoots and grain.
Subcellular locations: Nucleus |
IRO2_ORYSJ | Oryza sativa subsp. japonica | MEQLFVDDPAFASSMSSLEADIFSGAGQLPSSPWLDLDLDDDVQDLSMAPTTANAVSSGYGSGGSGSHRKLSHNAYERDRRKQLNELYSSLRALLPDADHTKLSIPTTVSRVLKYIPELQKQVENLERKKKELTTTSTTNCKPGVLGSQLMSEGMAPIVSATCINDMEIMVQVSLLSNVAGSVLPLSKCIKVLENEGLHFISSSTSSGFGNRTFYSIHLQRSEGTINEECPAFCERLEKVVRNKAKL | Transcription activator that binds to the DNA motif 5'-CACGTGG-3' in the promoter of iron (Fe) deficiency-inducible genes as well as of genes involved in iron homeostasis, thus contributing to basal tolerance to iron deficiency, iron uptake from soil and iron transport, particularly during seed maturation and germination ( , ). Promotes the accumulation of mugineic acid family phytosiderophores (MAs) . Required for ethylene-mediated signaling during iron deficiency responses . Improves growth and yield, especially in calcareous soil with low iron availability. Promotes iron concentration in shoots and grain .
Subcellular locations: Nucleus, Cytoplasm
Localized partially to the nucleus under iron deficiency conditions.
Expressed constitutively at low levels in the roots (, ). Also observed in flowers, developing seeds, embryos and vascular bundles . |
IRO3_ORYSJ | Oryza sativa subsp. japonica | MVPSERGDVATAIRPAAADKLVHGPISDKKCRKKVPRKVHKSEREKLKRGHLNDLFGELGNMLEADRQSNGKACILTDTTRILRDLLSQVKSLRQENSTLQNESNYVTMERNELQDENGALRSEISDLQNELRMRATGSPGWGHGATGSPLPVPPSPGTVFPSQQPMQPSPMTTSTVFPLQQPLPQPTVIEPSARQPLELKLFLEAPPAEDPEPSEDQEAPNNVARPQPRYPTEASSWPISLGLPRMEDEQM | Transcription factor that acts as a negative regulator of the iron deficiency response . Suppresses the induction of iron deficiency responsive genes, such as NAS1, NAS2, IRO2, IRT1, YSL15, and NRAMP1 .
Subcellular locations: Nucleus |
ITPK2_ORYSJ | Oryza sativa subsp. japonica | MRLHGEVSFDEDEEEVVMVPAAALSSSPLNGGAVPVTRLVVGYALTKKKVKSFLQPNLLLLARKKGINLVAIDDTRPLAEQGPFDVILHKITSKEWQQVLEDYHEEHPEVTVLDPPNAINHLNNRQSMLAEVSDLNLSSFYGEVCTPRQLVIMRDPSSIPTAVAMAGLTLPLVAKPLVVDGTSKSHELSLAYDEASLSMLDPPLVLQEFVNHGGILFKVYIIGETIQVVRRFSLPDVNTYDLLNNVGVYRFPRVSCAAASADHADLDPHISELPPRPLLEKLGKELRGRLGLRLFNIDMIRELGTKDRYYIIDINYFPGFGKMPGYEHIFTDFLLNLAQSKYKKCLSGG | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds (By similarity). May be involved in the negative regulation of osmotic stress signaling (, ).
Subcellular locations: Endoplasmic reticulum
Expressed in roots, leaves, flowers, anthers and embryos. |
ITPK2_SOYBN | Glycine max | MSESEVAGQRYRVGYALQGKKVESFIQPSLLDHAKQHSIDLVQIDPTAPLQQQGPFHCIIHKLHTQHWKNLLQQFSSKHPNTVIIDPPELVDRLHNRVSMLDAVTHLQFSLENATIGVPKQVVVNEPKSFDLHKFEEEQGLRFPVIAKPLAADGGAGSHELCLVFDEEGLHALSVPMVLQEFVNHGGVVFKIYVAGQRVNCVKRKSLGDITEEKLKVLRGSLPFSRVSSLGVEDEGGGAVEDAEMPPQSLVGELARGLREALGLNLFNVDVIRDGKEPTRYLVIDINYFPGYAKLPSYEPFITDFLLDIVRSKTA | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4, Ins(3,4,6)P3 and Ins(1,3,4)P3 . May participate in an inositol lipid-independent pathway of InsP6 synthesis . Barely able to add a beta-phosphate to InsP6 to yield 5-InsP7, thus exhibiting negligible InsP6 kinase activity . Has also Ins(1,3,4,5,6)P5 phosphatase activity . Probably involved in the regulation of drought and salinity tolerance by diverting the flux of inositol phosphate pool towards phytate biosynthesis .
Expressed in seeds (, ). Mainly expressed in seedlings, and, to a lower extent, in roots, flowers, stems and leaves (, ). |
ITPK3_ORYSI | Oryza sativa subsp. indica | MVSGGRVGGGEGEAGEAAEVAVAMVDNEEEVAQAQAPPAAAVAARELVVGYALTSKKAKSFLQPKLRGLARKKGILFVAIDQKRPLSDQGPFDIVLHKLTGREWQQLLEEYREEHPEVTVLDPPGAIEHLLNRQSMLQEVSELDLSDCHGRVGVPKQLFVNTDPSSIPAAVMRAGLSLPLVAKPLVAKSHELSLAYDPISLTKLEPPLVLQEFVNHGGVLFKVYIVGDAIRVVRRFSLPNVDVGDLSNNAGVFRFPRVSCASANADDADLDPHVAELPPRPLLEILARELRRRLGLRLFNIDMIREHGTRDRFYVIDMNYFPGYGKMPGYEHVFTDFLLSLVQKEYKRRPSYSSCEG | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds. |
ITPK3_ORYSJ | Oryza sativa subsp. japonica | MVSGGRVGGGEGEAGEAAEVAVAMVDNEEEMAQAQAPPAAAVAARELVVGYALTSKKAKSFLQPKLRGLARKKGILFVAIDQKRPLSDQGPFDIVLHKLTGREWQQLLEEYREEHPEVTVLDPPGAIEHLLNRQSMLQEVSELDLSDCHGRVGVPKQLFVNTDPSSIPAAVMRAGLSLPLVAKPLVAKSHELSLAYDPISLTKLEPPLVLQEFVNHGGVLFKVYIVGDAIRVVRRFSLPNVDVGDLSNNAGVFRFPRVSCASANADDADLDPHVAELPPRPLLEILARELRRRLGLRLFNIDMIREHGTRDRFYVIDMNYFPGYGKMPGYEHVFTDFLLSLVQKEYKRRPSYSSCEG | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds.
Expressed in roots, leaves, flowers, anthers and embryos. |
ITPK3_SOYBN | Glycine max | MRLREEVACKNDDVCEKEEVVIENDVTVAQNHWCPVVNAGFSSPKRVVVVGYALTTKKIKSFLQPKLEGLARNKGILFVAIDHNRPLSDQGPFDIVLHKLSGKEWRQVLEDYRLSHPEVTVLDPPDAIQHLRNRQYMLQAVADMNLSDSYGIVGVPRQLVIKRDALAIPELVNKAGLTLPLVAKPLVADGSAKSHELSLAYEHFSLQNLEPPLVLQEFVNHGGVLFKVYIVGDAIKVVRRFSLPDVSKWELSKDAGIYRFPRVSCAAASADDADLDPTVAELPPRPLLEKLAKELRWRLGLRLFNLDIIREYGTRNHFYVIDINYFPGYGKMPEYEHIFTDFLLSLGQGKYKKK | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4, Ins(3,4,6)P3 and Ins(1,3,4)P3 . May participate in an inositol lipid-independent pathway of InsP6 synthesis .
Seed specific. |
ITPK4_ORYSI | Oryza sativa subsp. indica | MAPELSSPSSSPRYTVGYALLPEKVSSVVRPSLVALAADRGVRLVAVDVSRPLAEQGPFDLLVHKMYDRGWRAQLEELAARHPGVPVVVDSPGAIDRLLDRATMLDVVSGLRTPVSVPPQVVVSDAAADADELLARAALRFPLIAKPLAVDGSAESHDMRLVYRRDGVLPLLRAPLVLQEFVNHGGVLFKVYVVGDRATCVRRSSLPDVPARRLLDLDAEPSVPFANISNQPLPPPDDDGGAADDDTPAAGFVDEVARGLRRGLGLHLFNFDMIRERSEEHGDRYFIIDINYFPGYAKMPGYEAALTDFFLEMLRGTRPVPEQLGPGSGLDMEARKLEPGLGIGLRELESGRAQA | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds. |
ITPK4_ORYSJ | Oryza sativa subsp. japonica | MAPELSSPSSSPRYTVGYALLPEKVSSVVRPSLVALAADRGVRLVAVDVSRPLAEQGPFDLLVHKMYDRGWRAQLEELAARHPGVTVVVDSPGAIDRLLDRATMLDVVSGLRTPVSVPPQVVVSDAAADADELLARAALRFPLIAKPLAVDGSAESHDMRLVYRRDGVLPLLRAPLVLQEFVNHGGVLFKVYVVGDRATCVRRSSLPDVPARRLLDLDAEPSVPFANISNQPLPPPDDDGGAADDDTPAAGFVDEVARGLRRGLGLHLFNFDMIRERSEEHGDRYFIIDINYFPGYAKMPGYEAALTDFFLEMLRGTRPVPEQLGPGSGLDMEARKLEPGLGIGLRELESGRAQA | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds.
Highly expressed in embryos and at lower levels in roots, leaves, flowers and anthers. |
ITPK4_SOYBN | Glycine max | MRLNGEISSGEEEEEEKQTGTTTFSSQKVVVGYALTSKKKKSFLQPSFTGLARNRGINFVAIDLNKPLPEQGPFDIILHKLSGEVWREIIEDYREKHPEVTVLDPPDAIQHLHNRQSMLQDVLDLNLSDCHGKVGVPRQLVITKEKDPSSIPYEVTKAGMKLPLVAKPLVVDGTAKSHELFLAYDEFSLSAVEPPLVLQEFVNHGGLLFKIYIVGETIKVVRRFSLPNISKRELSKVAGVFRFPRVSCAAASADDADLDPNIAEHPPRPLLERLARELRHRLGLHLFNIDMIREYGTKDVFYVIDINYFPGYGKMPGYEHVFTDFLLSLVESKCSNKKLAA | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4, Ins(3,4,6)P3 and Ins(1,3,4)P3 . May participate in an inositol lipid-independent pathway of InsP6 synthesis .
Expressed in seeds. |
ITPK5_ORYSI | Oryza sativa subsp. indica | MAGDEPLPGDGQRRRYLIGYALAPKKQQSFIQPSLVSRAAGRGMDLVPVDPSRPLPEQGPFHLLIHKLYGEEWRGQLDAFSAAHPAVPVVDPPHAIDRLHNRISMLQVVSELDVPLHAHHHHTFGIPSQVVVYDAAALSDSGLLAALRFPLIAKPLVADGTAKSHKMSLVYHREGLRKLRPPLVLQEFVNHGGVIFKVYVVGAHVTCVKRRSLPDVSSDVLQDASAEGSLSFSQVSNLPNERTAQEYYDDMRLEDAIMPPTAFINDIAAALRRALGLHLFNFDMIRDARAGDRYLVIDINYFPGYAKMPGYETVLTDFFWEMVHKDDDTPNLNPNPNDEDVK | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds. |
ITPK5_ORYSJ | Oryza sativa subsp. japonica | MAGDEPLPGDGQRRRYLIGYALAPKKQQSFIQPSLVSRAAGRGMDLVPVDPSRPLPEQGPFHLLIHKLYGEEWRGQLDAFSAAHPAVPVVDPPHAIDRLHNRISMLQVVSELDVPLHAHHHHTFGIPSQVVVYDAAALSDSGLLAALRFPLIAKPLVADGTAKSHKMSLVYHREGLRKLRPPLVLQEFVNHGGVIFKVYVVGAHVTCVKRRSLPDVSSDVLQDASAEGSLSFSQVSNLPNERTAQEYYDDMRLEDAIMPPTAFINDIAAALRRALGLHLFNFDMIRDARAGDRYLVIDINYFPGYAKMPGYETVLTDFFWEMVHKDDDTPNLNPNPNDEDVK | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds.
Expressed in roots, leaves, flowers, anthers and embryos. |
ITPK6_ORYSI | Oryza sativa subsp. indica | MPSMRVTTDTWPRRAAQEPLLLLLLRSSLMKSASLQALNPNRAMAAMGRSVRVVLDSSVLLDPSGVTAEEEEVVVALRPGAEALLRRLRYSNLRVAICHPEGLTTNESGFLEKTAKLYSFGYMPLTSPSGSNLLNELMLEWSETNFCFYVTSGVHEGLLSELQNHNWEVIAMGNEDVIKNSGVIHISMLQELLITLATSIKKEIGNSSAFVVGYVMKQSREEDFAKRGAFPIYPSKNDLIFVPLSFELPLASQLQEVDLVLHKITDEIINIDPNSSISFPKGISFSPGMSEIIRFVEEHCDFCVIDPFKNIYPLLDRIQIQEILIRLEGLSAEGRPKLRAPCFLKIESFCGSELQKQLAEAKLSFPLIVKPQVACGVADAHNMALIFKIEEFSNLSVPLPAILQEYIDHGSKIFKFYAIGDKIFHAIKNSMPNASHLKSSSGGKPLTFNSLKTLPVATKEQLLQNEVQDSKLLDINLVEEAAKLLKELLGLTIFGFDVVVQESSGDHVIVDLNYLPSFKEVPDNVAMPAFWDAIKQSYESRKQMTQT | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds. |
ITPK6_ORYSJ | Oryza sativa subsp. japonica | MPSMRVTTDTWPRRAAQEPLLLLLLRSSLMKSASLQALNPNRAMAAMGRSVRVVLDSSVLLDPSGVTAEEEEVVVALRPGAEALLRRLRYSNLRVAICHPEGLPTNESGFLEKTAKLYSFGYMPLTSPSGSNLLNELMLEWSGTNFCFYVTSGVHEGLLSELQNHNWEVIAMGNEDVIKNSGVIHISMLQELLITLATSIKKEIGNSSAFVVGYVMKQSREEDFAKRGAFPIYPSKNDLIFVPLSFELPLASQLQEVDLVLHKITDEIINIDPNSSISFPKGISFSPGMSEIIRFVEEHCDFCVIDPFKNIYPLLDRIQIQEILIRLEGLSAEGRPKLRAPCFLKIESFCGSELQKQLAEAKLSFPLIVKPQVACGVADAHNMALIFKIEEFSNLSVPLPAILQEYIDHGSKIFKFYAIGDKIFHAIKNSMPNASHLKSSSGGKPLTFNSLKTLPVATKEQLLQNEVQDSKLLDINLVEEAAKLLKELLGLTIFGFDVVVQESSGDHVIVDLNYLPSFKEVPDNVAMPAFWDAIKQSYESRKQMTQT | Kinase that can phosphorylate various inositol polyphosphate such as Ins(3,4,5,6)P4 or Ins(1,3,4)P3 and participates in phytic acid biosynthesis in developing seeds. Phytic acid is the primary storage form of phosphorus in cereal grains and other plant seeds.
Highly expressed in embryos and at lower levels in roots, leaves, flowers and anthers. |
KAD2_ORYSJ | Oryza sativa subsp. japonica | MASSMAATATLSPPVLSAERPTVRGGLFLPPSPATSRSLRLQSARRCGISPATRKPRSLPRAAKVVVAVKADPLKVMIAGAPASGKGTQCELIKSKYGLVHISAGDLLRAEIAAGSENGKRAKEFMEKGQLVPDEIVVNMVKERLLQPDAQEKGWLLDGYPRSYSQAMALETLNIRPDIFILLDVPDELLVERVVGRRLDPVTGKIYHLKYSPPENEEIASRLTQRFDDTEEKVKLRLQTHYQNVESLLSIYEDVIVEVKGDALVDDVFAEIDKQLTSSLDKKTEMVASA | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism.
Subcellular locations: Plastid, Chloroplast |
KASC1_HORVU | Hordeum vulgare | MHAHAAHALGLRVPPPAFPRRRARPRRRPAAAVLATSAAPQRETDPRKRVVITGMGLASVFGSDVDTFYDRLLAGESGVGPIDRFDASSFPTRFAGQIRGFSSEGYIDGKNDRRLDDCIRYCILSGKKALESAGLGAGSDAHVKLDVGRAGVLVGTGMGGLSVFSDGVQNLIEKGYRKISPFFIPYAITNMGSALLAIDVGFMGPNYSISTACATSNYCFYAAANHIRRGEADIIVAGGTEAAIIPIGLGGFVACRALSQRNDDPITACRPWDKERDGFVMGEGAGVLVMESLEHAMKRDAPIIAEYLGGAVNCDAYHMTDPRADGLGVSSCITMSLRDAGVAPEEVNYINAHATSTLAGDLAEVRAIKQVFKNPSEIKINSTKSMIGHCLGAAGGLEAIATIKSITTGWVHPTINQFNPEPEVDFDTVANEKKQHEVNVGISNSFGFGGHNSVVVFAPFKP | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Specific for elongation from C-10 to unsaturated C-16 and C-18 fatty acids.
Subcellular locations: Plastid, Chloroplast |
KN5A_ORYSJ | Oryza sativa subsp. japonica | MDRRIGLTSPSPKSTEKSGRDLRSGGDANGGANTNSNSIPRGDKEKGVNVQVILRCRPMSDEETKSNTPVVISCNERRREVAATQIIANKQIDRTFAFDKVFGPASKQKDLFEQSISPIVNEVLEGYNCTIFAYGQTGTGKTYTMEGGGTRKTKNGELPTDAGVIPRAVRQIFDILEAQCAEYSMKVTFLELYNEEITDLLAPEEPKFPIVPEDKTKKPIALMEDGKGGVFVRGLEEEVVYSAGEIYKILDKGSAKRRTAETLLNKQSSRSHSIFSITIHIKELTHEGEEMIKIGKLNLVDLAGSENISRSGARDGRAREAGEINKSLLTLGRVINALVEHSGHVPYRDSKLTRLLRDSLGGKTKTCIIATISPSVYCLEETLSTLDYAHRAKNIKNKPEVNQRMMKSAVIKDLYSEIDRLKQEVFAAREKNGIYIPRERYLQEEAEKKAMTEKIERLGADLEARDKQLVELKELYDAEQLLSAELSEKLGKTQKDLEDTKNVLHDLEEKYNEAESTIKEKEYVIFNLLKSEKSLVDCAYNLRAELENAAADVSGLFSKIERKDKIEDGNRSLVQRFRSQLTNQLDTLHKTVSTSVMQQENHLKEMEDDMQSFVSSKDEAAQGLRESIQKLKLLHGSGITALDSLAGEIDMNSQSTFERLNSQVQSHTSSLEQCFGGIASEADNLLNELQCSLSKQEERLTQFAKKQREGHLRAVEASRSISKITAGFFSSLDVHASKLTSILEETQSVQDQQLLDLEKKFEECAANEEKQLLEKVAEMLASSHARKKKLVQTAVGNLRESAVNRTSHLQNEISTAQDFTSSVREKWGFYMEETEKNYIEDTTAVDSGRSCLAEVLVECKAKTTMGAQQWKNAEDSLFSLGKGNVESADSIVRTGTEANQSLRSKLSSAVSTTLEEIDIANKALLSSIDSSLKLDHDACANIGSIIKPCHEEISELKGGHYHRVVEITENAGKCLEEEYLVDEPSCSTPRRRQIDLPSMESIEQLRTPDYDELLKSFRESRASLKQANGDMKHFLEVQEATPPSITDPRAPLIARN | Responsible for microtubule translocation. May be important for the organization of phragmoplast-specific arrays of microtubules (By similarity). Plays an essential role in stabilizing the mitotic spindle. Required during mitotic cytokinesis (By similarity).
Subcellular locations: Cytoplasm, Cytoskeleton, Cytoplasm, Cytoskeleton, Spindle
Microtubule-associated. |
KN5B_ORYSJ | Oryza sativa subsp. japonica | MAQTPNPSRRSLVGPPPHPFLTPRPERRQLELRWADGGSQSSARRSGVGLTGGGGGGGGGSEMKDCEANVQVVLRCRPLSEEEQRANVQSAISCDDLKREVTVLHSLFKQADKTFTFDKVFGPKAQQRSIYDRAVKPIVKDVLEGYNCTVFAFGQTGTGKTYTMEGEMRQKASELSATAGVIPRAVRDIFDILEERKADYSMKVTFLELYNEEITDLLALEDQSRFPEDRQKRAISLMEDRKGGAVIRGLEEVVVYSASEIYNLLEHGSARRRTADTALNKQSSRSHSVFSIYIHVKETTVGNQELLKCGRLNLVDLAGSENIARSGAREGRAREAGEMNKSLLTLGRVITALVEHSVHVPYRDSKLTRLLRESLGGKAKTCIIATVSPSIHCLEETVVTLDYAYRAKSIKNKPEANQKVCKSVILKDLYQEMERMKQDVKAAREKNGIYIPQERFALEEAEKKTMRDKIEYLETQNKELKMNIESCKKEYLDLEEAHSRANISLKEKEFIISNLLHAEQSIVERAKDIRGALENASGDISALVDKLGRQSNTEAENKGLLFDFRSQLDHGLDLLHDTVVGCVCEQRQFLESMNEQNKIYFSAKSESTSQLERRIAKAKDIYASGVQCMNQLANTLHQRSIAHSEQMGLNILSHATRAANFLAVMVSEAEQVSNDVFKSISELKELLAFSADQQEVMFKRDLVSAQVMSKTSIDFFEDIRGHASRLIEHMEQSQAESSSQLLKFEEDFKELSVREEQAALDKIAGILAGLTAKKSTMVLDCVGQLNGKCREEQKHLKLQISNLQKVSDSGGKEAAAYAAKVESQFSEDKLSHCKIKDQMEDILQQSLKKTVHSVSYWSHTETSLEHLNKISVVEADDFIEETRKENESILQKMLIVSTQNDAKFAAITSDMLTAVKDSHLRDSESRMRIETVFATSSDHLEMLDTKHSQGTESIRSMTAKCLERDYKANSPVRRRPGELMTNAYSLESIEQLRTPVPDLVVKFRSENNLDEVDKGKRYVDQGTRTPRSPLMPVNHYNK | Responsible for microtubule translocation. May be important for the organization of phragmoplast-specific arrays of microtubules (By similarity). Plays an essential role in stabilizing the mitotic spindle. Required during mitotic cytokinesis (By similarity).
Subcellular locations: Cytoplasm, Cytoskeleton, Cytoplasm, Cytoskeleton, Spindle
Microtubule-associated. |
KN5C_ORYSJ | Oryza sativa subsp. japonica | MSSRQDKEKSVNVQVLLRCRPFSDDEVRSNAPQVITCNDYQREVAVTQTIAGKQIDRVFTFDKVFGPTAKQRDLYDQAIIPIVNEVLEGFNCTIFAYGQTGTGKTYTMEGECRRAKSGPKGQLPADAGVIPRAVKQIFDTLESQNTEYSVKVTFLELYNEEITDLLAPEEISKAALEERQKKPLPLMEDGKGGVLVRGLEEEIVTNASEIFSLLERGSAKRRTAETLLNKQSSRSHSLFSITIHIKEATPEGEELIKCGKLNLVDLAGSENISRSGAREGRAREAGEINKSLLTLGRVITALVEHLGHVPYRDSKLTRLLRDSLGGRTKTCIIATVSPSVHCLEETLSTLDYAHRAKSIKNRPEVNQKMMKSTLIKDLYGEIDRLKAEVYAAREKVGVYIPKDRYQQEENERKAMADQIEQMTTSLEANQKQINDLQEKYDSELQHSADLSKKLEATEKCLDHTSNLLSTTKEDLKQAQYNLKEKDYIISEQRKAENALIQQACLLRSDLEKSNRENAALYSKIARGDKLNAANRSVVNSFQADLASKLDILSTTLATSIDQQNKHLKSVENLCKSCVDSHDTATSEIKKKILASKALYMSHMEAFQNVVLLHKANSNSTLEDISSLSAASCCSLDQLLACVEGEAQKIFGDIQNLLADHRSEVAHFTQELRESFRISLDRTKDMSSFILGLFDKYVEETSKLQSHSNHTHEAQVKSLEDFQKAYEEQSKSEEQKLLADITSLVSKHVTRQRELVGGRLNSLGDAARGNKAFLDEHTSAMEVVTKDAKRKWEMFAEQAENDCKVGSNFSAAKHCRMETILQECACTVDTAAQQWKASHATVNDLCRKQIAEVEALVRSAIETNEQHEAEIASSRATAEEHASNSSKDLLQDVDNMLQEARNSSSRVVSTVEAHLGESQHLQESHSSHTAGINTHADNAFQSSYKDYEPTGETPVRSEPEVPSKDAIESLRAMPMESLMDEFRENHPYEPSKDRRPSLIPRSPLATINN | Responsible for microtubule translocation. May be important for the organization of phragmoplast-specific arrays of microtubules (By similarity). Plays an essential role in stabilizing the mitotic spindle. Required during mitotic cytokinesis (By similarity).
Subcellular locations: Cytoplasm, Cytoskeleton, Cytoplasm, Cytoskeleton, Spindle
Microtubule-associated. |
KN6_ORYSJ | Oryza sativa subsp. japonica | MVRLSTKPPNPKVEMNLKEPPITGAGAGAAASPPAPSTLRRNPPRSARPPPTPLPNSKPSQISRLLEEAAERLKVFLRIRPLPLPERKGKAKSPTNPKQVCLVANSPNSVALTVPHSKLLDPKRGRTEVFDGFSSVFSPDSSQHDVFSQVMNPLVDDLLLGGKSGLLVAMGPTGSGKTHTVFGSPRNPGLVPLTLRRIFSPTTHEPFSKLRSFCFSMFEILSEGKGERILDLLSDATDLVLQQSTIKGLKEVSVENFADAEALLFSGMLKRTTAATNANSKSSRSQCIITIRAVHKSSDAESENSLNNAVLTIADLAGAERERRTGNQGTRLLESNFINNTSMVFGLCLRSLLEHQKNKKKPLEKHFKNSMLTRYLRDYLEGRKKMTLILNVKPGDDDYLDTSFLLRQASPYMKIKYTNLEDSSGLVSQKRSSASLICQENTKKRKIHKVAGKDDIDKDDGVTISEKDESQYKLLNSELRRVSRNEEIMTNFARALWTVLKQYKQKLLESENAVESTRELLRSKDIKIMELEKKLKVLSCSCKKFPAVEDTFVEQNNDVSSGQVAQSFVSLSSQTDLVSIDSALNKSLAVEEVSEESTGHGPERSSDYDDKTGTGGSDVCDTSIIKLIAEEELCSGDCKPEKASSSDAFIPEHDVEKENIGIVVQVLDKKLDRSESCSDGGGVTHSSSSLDHPSDQSFTDTCLQNESANLSPQFIGASKKSPIEQSEEEREEIHNITTEGIQQNVHTRGVKHHSTPSCSQEVNSGSLHVSSSQLQGMGALQQDPQSERCKPTVEITIVEYGCAQPPHVVDDHGGMYPCTLNGKSSPRKAPISPTKDNQAEKLTDKIEDLSASKPCNRKNTRRRLQPVSAMMLKEFTGPDIFVDTRKEEKVKSSRDAMGRSDKLIRLLTDHPPRARGRAQ | null |
KN7A_ORYSJ | Oryza sativa subsp. japonica | MGVSRPPSTPASKIERTPMSTPTPGGSTRVKEEKIFVTVRVRPLSKKELALKDQVAWECDDNQTILYKGPPQDRAAPTSYTFDKVFGPASQTEVVYEEGAKDVAMSALTGINATIFAYGQTSSGKTFTMRGVTESAVNDIYRHIENTPERDFIIKISAMEIYNEIVKDLLRPESTNLRLLDDPEKGTIVEKLEEEIAKDSQHLRHLISICEEQRQVGETALNDTSSRSHQIIRLTVESRLREVSGCVKSFVANLNFVDLAGSERAAQTHAVGARLKEGCHINRSLLTLTTVIRKLSSDKRSGHIPYRDSKLTRILQLSLGGNARTAIICTMSPAQTHVEQSRNTLFFATCAKEVTNNAKVNMVVSDKQLVKHLQMEVARLEAELRTPDRASSSEIIIMERDRKIRQMEKEMEELKKQRDNAQLKLEELQKKMGDNQPGWNPFDSPQRTRKCLTYSGSLQPSNKMKIRSSIRQSATAPFMLKHEIRKLEQLQQQLEVEANRAIEVLHKEVECHKHGNQDAAETIAKLQAEIRGMQSVRSDRDVDMITDEGNGSDLKEEISRLHMQDNDIAKLEAKLENVQRSIDRLVMSLPNVGTQCNETTPKSNRAKKKKRMLLPLGVSNINRPNLIRAPCSPLSSSRPLEPEVENRAPEGDTVSHEGSERATPTKSEDTGDVSSRDETPRYRRSSSVNMKKMQKMFQNAAEENVRNIRAYVTELKERVAKLQYQKQLLVCQVLELESNEGKTNDMEEDSEENAGSLQDGPDSWDRLFKEQMQHIIQLWDLCHVSIIHRTQFYLLFRGDRADQIYIEVEVRRLTWLQQHFAEVGDASPAAGDDSTISLASSIKALRNEREFLARRMGSRLTEEERERLFIKWQVPLEAKQRKLQLVNRLWTDPNDQAHIDESADIVARLVGFCEGGNISKEMFELNFAVPASRKPWLMGWQPISNMIREKTQLW | May be essential to promote the progression of cytokinesis during node-internode differentiation.
Ubiquitous with a preferential expression in the shoot apical meristem (SAM). |
KN7B_ORYSJ | Oryza sativa subsp. japonica | MRAIQKKSLCHTSIISCWRRREYSIPPQANFGETFLNEKSSRSHQILRLTVESSAREFLGKDKSTTLVASANFVDLAGSERASQALSAGTRLKEGCHINRSLLALGTVIRKLSMGSNAHIPYRDSKLTRILQPSLGGNARTAIICTLSPATSHIEQSRNTLLFGSCAKEVVTNAQVNVVMSDKALVKHLQKELARLESELRHPVQSSSLETLLKEKDNQIRKMEKEIKELKSQRDLAQSRLQDLLQSVGDHDLNRQVQGKHSVRSPPSVGMPPSVSRDDSSQVSHDDSDLYKEVRCIESNRTGGNDQLDLSAGESSSPQDSNMNSGLHGNDSNASVNSRHSRPSGEAPITLEEHLENIRRPFVSLAKDLGSSTRNSSNLRVIGRSRSCRSLTGSTMFDDMEMDDCTPLNRSLVEFPGRPVESHRRGSALHYDAETDTLSRAGSMSSEISTFKDAKTNGSVACDTEFTGIGEFVAELKEMAQVHYQKQLGDQNANGKSIGLDPIEGVSQSPSRWPLEFEKKQQEIIELWQACSISLVHRTYFFLLFKGEAADSIYMEVELRRLSFLRDTYSRGSTPSNAIVGSLSTSPVASAKKLQREREMLARQMQKRLSTEEREHTYTKWGVSLDSKRRKLQVARRLWTETKDLEHVRESASLVAKLIGLQEPGQVLKEMFGLSFAPQQQPTRRRSSNGWRYGIPSFA | null |
KN7C_ORYSJ | Oryza sativa subsp. japonica | MGAIGGDELVQWDKMGAAEAVNGGCGGAGKMDRIQVLVRLRPLSEKEVARREPAEWECINDSTVMFRSTFPDRPTAPTAYTFDRVFHSDCSTKEVYEEGVKEVALSVVSGINSSIFAYGQTSSGKTYTMTGVTEYTVADIYDYINKHEERAFVLKFSAIEIYNEVIRDLLSAENTPLRLWDDAEKGTYVENLTEVVLRDWNHLKGLISVCEAQRRTGETFLNEKSSRSHQILRLTVESSAREFLGKDKSTTLVASANFVDLAGSERASQALSAGTRLKEGCHINRSLLALGTVIRKLSMGSNAHIPYRDSKLTRILQPSLGGNARTAIICTLSPATSHIEQSRNTLLFGSCAKEVVTNAQVNVVMSDKALVKHLQKELARLESELRHPVQSSSLETLLKEKDNQIRKMEKEIKELKSQRDLAQSRLQDLLQSVGDHDLNRQVQGKHSVRSPPSVGMPPSVSRDDSSQVSHDDSDLYKEVRCIESNRTGGNDQLDLSAGESSSPQDSNMNSGLHGNDSNASVNSRHSRPSGEAPITLEEHLENIRRPFVSLAKDLGSSTRNSSNLRVIGRSRSCRSLTGSTMFDDMEMDDCTPLNRSLVEFPGRPVESHRRGSALHYDAETDTLSRAGSMSSEISTFKDAKTNGSVACDTEFTGIGEFVAELKEMAQVHYQKQLGDQNANGKSIGLDPIEGVSQSPSRWPLEFEKKQQEIIELWQACSISLVHRTYFFLLFKGEAADSIYMEVELRRLSFLRDTYSRGSTPSNAIVGSLSTSPVASAKKLQREREMLARQMQKRLSTEEREHTYTKWGVSLDSKRRKLQVARRLWTETKDLEHVRESASLVAKLIGLQEPGQVLKEMFGLSFAPQQQPTRRRSSNGWRYGIPSFA | null |
KN7D_ORYSJ | Oryza sativa subsp. japonica | MATRPASRQRRASSAAAAVAVVRSSPQPQQQQQQQLPIPQSGSPTSTTTTTTSSSRLTPELSLDGPASPLFAGLDEDPAPKENVTVTVRFRPLSPREIRQGEEVAWYADGDTVVRSEQNPSVAYAYDRVFAPTTTTRQVYDVAAQHVVSGAMEGVNGTIFAYGVTSSGKTHTMHGDQRSPGIIPLAVKDAFSIIQETPNREFLLRVSYLEIYNEVVNDLLNPAGQNLRIREDPQGTFVEGIKEEVVLSPAHALSLIAAGEEHRHVGSTNFNLLSSRSHTIFTLTVESSPCGESNEGEAVTFSQLNLIDLAGSESSRAETTGVRRKEGSYINKSLLTLGTVISKLTDGKATHIPFRDSKLTRLLQSSLSGQGRVSLICTVTPASSNSEETHNTLKFAHRAKRIEVQASQNKIIDEKSLIKKYQNEIRRLKEELEQLKMGIITGTPVKDAGEDNIILWKQKLEDGNVKLQSRLEQEEEAKAALLARIQRLTKLILVSTKATQTSRFSPHPGPRRRHSFGEEELAYLPYKRRDIVLDNESNELLSPVEGLGMTLEDSKEEKKNRKGILNWFKLRKREGGASILTSSEGDKSSLTKSTAPSTPIGESVNFPSEPRISNSLVGESASVDLFSIGHGEFATDSLHGEETPLASRKTIDHVDLLREQLKILSGEVALHTSVLKRLTEEAGRSPNNEKIQMEMKKVNDEIKGKKHQIASLERQIPHSISNNQGMADKLELTPSYAELLEQLNEKSFDLEVKAADNRVIQDQLNEKTTECMELQEEVAHLKEQLYQTLQAKDSLSNSIMMQKNAGINHETDNHADQELSVPREVPGETSPKEPQSVEIDELKQKVCELIEVKAQLETRNQKLLEESTYAKGLASAAGVELKALSEEVTKLMNQNEKLASELASVRSPTPRRANSGLRGTRRDSISRRHEPAPRRDNNAGYEREKALEAVLMEKEQKEAELQRRIEESKQKEAFLESELANMWVLVAKLKKSQGHDLEDFDTKYIGS | Probable minus end-directed motor protein with a microtubule-enhanced ATPase activity. Binds ATP/ADP in vitro. Retains total enzymatic activity even after the removal of the ADP bound in the active site.
Subcellular locations: Plastid, Chloroplast |
KSL10_ORYSJ | Oryza sativa subsp. japonica | MLPSSICSMGQIPRTSPHYYGMLPKQMSKGHPPMVTRAVGGVEKGEVGGNVRSLQVMHSKELQAKIRKQLQRVELSPSLYDTAWVAMVPERSSSQAPCYPQCIEWILQNQHDDGSWGINSSSLSVNKDILLSTLACVVALKKWNAGSYHIKRGLNFVGRNFSVAMDVQNIAPVGFNVTFSGLITLASGMGLQLPVWQTDIDEIFHLRKIELERDSGGTISARKAFMAYVAEGFGSLQDWDQVMAYQRKNGSLFNSPSTTAAAAIHTFNDRTLNYLDSLTNKFGGPVPAMYPQNIYSQLCTVDALERTGISQKFAREIRDILDTTYRSWLHNEEEVMLDIPTCAMAFRLLRTHGYDITSDEMAHFSEQSSFDDSIHGYLNDTKTLLELFKTSQIRFSCEDLVLENIGTWSAKLLKQQLLSNKLSTSAQSEVEYVLKFPLHSTLDRLEHRRNIEQFKVEGSKVLKSGYCGSHSNEEILALAVDYFHSSQSVYQQELKYFESWVKQCRLDELKFARVMPLIVHFSSAATIFAPELADARMVLSQTCMLITVYDDFFDCPEISREEKENYIALIEKWDNHAEIGFCSKNVEIVFYAVYNTYKQIGEKAALKQNRSIMDQLVEDLVSSAKAMMVEADWTATKYIPATMEEYMSNAEVSGAFASFVCPPLYFLGLKLSEEDVKSHEYTQLLKLTNVIGRLQNDSQTYRKEILAGKVNSVLLRALTDSGNTSPESIEAAKEIVNRDAESSMVEMRSLVFSEGGPIPRPCKDRFWEMCKIVFYFYSEDDAYRTPKETMSSARAVILDPLRLIPPPSCPETLSS | Involved in the biosynthesis of oryzalexin A-F phytoalexins. Catalyzes the conversion of ent-copalyl diphosphate to the phytoalexin precursor ent-sandaracopimaradiene.
Subcellular locations: Plastid, Chloroplast |
KSL11_ORYSI | Oryza sativa subsp. indica | MMLLSSSYSGGQFPGVSPLGTRPKRSTTVVPLPVVTRATAGGVRNNLEVVGNAGTLQGMDIDELRVIVRKQLQGVELSPSSYDTAWVAMVPVQGSPQSPCFPQCVEWILQNQQEDGSWGHSAGPSGEVNKDILLSTLACVLALNTWNVGQDHIRRGLSFIGRNFSVAIDGQCAAPVGFNITFSGMLHLAIGMGLKFPVMETDIDSIFRLREVEFERDAGGTASARKAFMAYVSEGLGREQDWDHVMAYQRKNGSLFNSPSTTAASAIHSCNDRALDYLVSLTSKLGGPVPAIHPDKVYSQLCMVDTLEKMGISSDFACDIRDILDMTYSCWMQDEEEIMLDMATCAKAFRLLRMHGYDVSSEGMARFAERSSFDDSIHAYLNDTKPLLELYKSSQLHFLEEDLILENISSWSAKLLKQQLSSNKIMKSLMPEVEYALKYPLYSTVDALEHRGNIERFNVNGFQRPKSGYCGSGADKEILALAVDKFHYNQSVYQQELRYLESWVAEFGLDELKFARVIPLQSLLSALVPLFPAELSDARIAFSQNCMLTTMVDDFFDGGGSMEEMVNFVALIDEWDNHGEIGFCSNNVEIMFNAIYNTTKRNCAKAALVQNRCVMDHIAKQWQVMVRAMKTEAEWAASRHIPATMEEYMSVGEPSFALGPIVPLSAYLLGEELPEEAVRSPEYGQLLRHASAVGRLLNDVMTYEKEVLTWTPNSVLLQALAAARGGGESPTPPSPACAEAARGEVRRAIQASWRDLHRLVFRDDDGSSIVPRACRELFWGTAKVANVFYQEVDGYTPKAMRGMANAVILDPLHLQQ | Catalyzes the conversion of syn-copalyl diphosphate to stemodene. |
KSL2_ORYSJ | Oryza sativa subsp. japonica | MVPALRRGGGGPRFPQCVAWIQRNQRGDGSWRHAAAAHQQLGSSPEIVTERDLSSTLACVLALARWDAGSEHVRRGLQFIGRNMSVAMDDQTAAPASGSVVSFAAMLRMAMEMGLEVPAVSQADVRDRDAGVICHGGRTEYTAYVSEGLGNIQNWNEVMKFQRKNGSLFNSPYTTAAALVHNYDAKALQYLDMLLDKFGSAVPAAYPANIQSQLYMVDVLEKMGISRHFVGEIKSILDMTYSCWKQRDEEIVLDMQTCGMAFRMLRMNGYDVSSDELSHFSEPSSFHNSLQGYLNDTRSLLELHKASKVSIAEKEVILDNIGSWTGCLLKEQLLSSAMKRNPLSEEVEYALEFPFYTILDRLDHKRNIEHFDITSSQMLETAYLPCHSNEEIMALGVRDFSSSQFIFQEELQQLNSWVKESRLDQLQFARQKLDYFYFSAAATIFTPELSDVRILWAKNGVLTTVVDDFFDVGGSKEELENLVALVEKWDKNDKTEYYSEQVEIVFSAIYTSTNQLGSMASVVQGRDVTKHLVEIWQELLRSMMTEVEWRQSRYVPTAEEYMENAVVTFALGPVVLPALYLVGPKMPDSVIRSQECSELFRLMSKCGRLLNDVQSYEREGSQGKLNSVSLLALHSGGSVSMEEAVKQIQRPIEKCRRELLKLVVSRGGAVPRPCRELFWSMCKVCHFFYSGGDGFSSPTAKAGALDAIPICFVECDEKKKNEEERIVIFWAEKKEKEKEKERVNNKKMVLLLFTWVTGDDGGGAAEVAGATGGLGHLPVAVEGVGGVGEHDPGVLGVKPGVDDAGGLGSNDGGVKPPMGGSGGGWSSGANGVEAKGGVGVGVVVGVEDDGGAFGGLTQYGELEPSPVASARLAASPSGFAGEGDEEGSCIGSTVLMKLSLYSAFSSVFLLLRLIRALASAPSTTTTTTQSNAHQKPN | Expressed in roots. |
KSL3_ORYSJ | Oryza sativa subsp. japonica | MFQLELVNVVMHQRKAIEDTMRKKKKQQLHKFEMLPSPYDTAWVAMVPLPGSSSQLPCFPQCVEWILQNQQSNGSWDLNQLDSITKDALLSTLACVLALRRGLLFIGRNFSIAMDEQLAAPIGFNITFPGMLSSVIEMGLEVPIGQTDVERVLHLQETELKREYEENYRGRNTYMAYVSEGLGNAQDWNEVMNFQRKNGSLFNSLSITAAVLVHNYDAKAHRYLNLLLNKFGTAVYTKNIHRQLSMLDALENMGISRHFDGEIKSILDMTYSCWLQRDEEVMLDITTCAMAFRILRMNGYDVSSDDLCHIAEVSDFHSSHQGYLSDTRTLLELYKASEVSVADNEFILDRIGSWSGRLLKEQLSSGALQRTSSIFEEVEHALDCPFYATLDRLVHKRNIEHFAAMSYISYAQNNIPDELERIDSWVKENRLHELKFARQKSAYFYLSAAGTVFDPEMSDARIWWAINGVLTTVVDDFFDVGGSREELENLISLVEMWDEHHKEELYSEQVEIVFFAIFNSVNQLGAKVSAVQGRDVTKHLIEIWLDLLRSMMTEVEWRISNYVPTPEEYMENAAMTFALGPIVLPALYLVGPKIPESVVRDSEYNELFRLMSTCGRLLNDVQTYEREDGEGKVNSVSLLVIQSGGSVSIEEARREIMKPIERCRRELLGLVLRRGSAVPGPCKELFWKMCKVCYFFYSRGDGFSSPTAKSAAVDAVIRDPLDLAAVVASQEPIYIIPAS | Expressed in roots and stems. |
KSL4_MAIZE | Zea mays | MASLSFASSHASLFCCQQSSSAIILRPAGALLRLSRRQPSSHTISTTDQLFPRRSRMPRNVDTHAAAERNSPSTMSSLEAVDELETNGDSAVVVVREQQQQQHLLMGATDDGLPPSPYDTAWVAMVPAPGNPLVPRFPQCVDWILQNQRSDGSWGPDGGSGDHPSSPLGKDALMSTLACVLALKTWDAGEEHVRKGLSFVGNNSPSCVMTGDERDAPVGFSVIFPGMLARAIDMGLDIPMMTQANVDAFIRLRDTELNRMAATTGSKAFMSYVAEGLGDVLDWDEAAMVYQRQNGSFFNSPATTAAAAIHGNNDRALRYLDSLVNMFGSSVPTVYPRSTYSRLHMVDTLQKMGLSRSFVSEINEMLDMTYRSWLANDDEEMMLDMSTCAMAFRLLRMHGYDVSSDGLAQFSSESSFRDSVHGQANDTEALLELYKASQIQITEDELVLVDIRSWSAKLLKEQLGSDKVSRSVDAQEVQQVLKFPFYTTLDRLEHRRHIEQFKAGGFHMLKSAYRFCKEDEELVSLAVQGFHSSQALYQQELQFLTRWAKEARLHDLEFARIMPMNTFFPNAALMYAPELSEARILCTKNCMLATAVDDLFDVGGSREEMENLVRLIDMWDEHEEVGFCSERVEILFRAIYDTSKELAAKAMAVQNRSVINHVAELWADLVRAMMTEAEWSMRGHVPSSMEEYMQVAETSFALGPIVLMPLYLIGPELPEAVVRCPEYKQLFHHMNVCGRLLNDLQSYEREAKQGKINSVLLVAPRHGGSIEAAKSEVRRAIEASRRELLRMLVAEADATVPRPFRQEFWNMCKMVHLFYMEDDCYSSPKELVHAANMVVFDPLRVREL | Involved in the production of antifungal dolabralexin phytoalexins in response to biotic and abiotic stresses . In response to fungal infection and in associtation with AN2, is involved in the production dolabradiene, a type of antifungal phytoalexin . Converts ent-copalyl disphosphate (ent-CPP) to dolabradiene .
Subcellular locations: Plastid, Chloroplast |
KSL4_ORYSI | Oryza sativa subsp. indica | MASPMEAVARSSLVLAPRRRRALGLLPAAAAPFVLDCRRRHNGGMRRPHVSFACSAELDTGRRQLPSTGTRAVMSSCPGYVEGRMVGENTSQINMGREARIRRHLENPEFLPSSYDIAWVAMVPLPGTDHLQAPCFPECVEWILQNQHSNGSWGVNEFDSSASKDILLSTLACIIALEKWNVGSEQIRRGLHFIAKNFSIVIDDQIAAPIGFNLTFPAMVNLAIKMGLEFPASEISIDQILHLRDMELKRLSGEESLGKEAYFAYIAEGLEESMVDWSEVMKFQGKNGSLFNSPAATAAALVHRYDDKALGYLYSVVNKFGGEVPTVYPLNIFSQLSMVDTLVNIGISRHFSSDIKRILDKTYILWSQRDEEVMLDLPTCAMAFRLLRMNGYGVSSDDLSHVAEASTFHNSVEGYLDDTKSLLELYKASKVSLSENEPILEKMGCWSGSLLKEKLCSDDIRGTPILGEVEYALKFPFYATLEPLDHKWNIENFDARAYQKIKTKNMPCHVNEDLLALAAEDFSFCQSTYQNEIQHLESWEKENKLDQLEFTRKNLINSYLSAAATISPYELSDARIACAKSIALTLVADDFFDVGSSKEEQENLISLVEKWDQYHKVEFYSENVKAVFFALYSTVNQLGAMASAVQNRDVTKYNVESWLDYLRSLATDAEWQRSKYVPTMEEYMKNSIVTFALGPTILIALYFMGQNLWEDIVKNAEYDELFRLMNTCGRLQNDIQSFERECKDGKLNSVSLLVLDSKDVMSVEEAKEAINESISSCRRELLRLVVREDGVIPKSCKEMFWNLYKTSHVFYSQADGFSSPKEMMGAMNGVIFEPLKTRGN | Involved in the biosynthesis of momilactone A and B phytoalexins. Catalyzes the conversion of syn-copalyl diphosphate to the phytoalexin precursor syn-pimara-7,15-diene.
Subcellular locations: Plastid, Chloroplast |
KSL4_ORYSJ | Oryza sativa subsp. japonica | MASPMEAVARSSLVLAPRRRRALGLLPAAAAAAPFVLDCRRRHNGGMRRPHVSFACSAELDTGRRQLPSTGTRAVMSSCPGYVEGRMVGENTSQINMGWEARILRHLENPEFLPSSYDIAWVAMVPLPGTDHLQAPCFPECVEWILQNQHSNGSWGVNEFDSSASKDILLSTLACIIALEKWNVGSEQIRRGLHFIAKNFSIVIDDQIAAPIGFNLTFPAMVNLAIKMGLEFPASEISIDQILHLRDMELKRLAGDESLGKEAYFAYIAEGLEESMVDWSEVMKFQGKNGSLFNSPAATAAALVHRYDDKALGYLYSVVNKFGGEVPTVYPLNIFSQLSMVDTLVNIGISRHFSSDIKRILDKTYILWSQRDEEVMLDLPTCAMAFRLLRMNGYGVSSDDLSHVAEASTFHNSVEGYLDDTKSLLELYKASKVSLSENEPILEKMGCWSGSLLKEKLCSDDIRGTPILREVEYALKFPFYATLEPLDHKWNIENFDARAYQKIKTKNMPCHVNEDLLALAAEDFSFCQSTYQNEIQHLESWEKENKLDQLEFTRKNLINSYLSAAATISPYELSDARIACAKSIALTLVADDFFDVGSSKEEQENLISLVEKWDQYHKVEFYSENVKAVFFALYSTVNQLGAMASAVQNRDVTKYNVESWLDYLRSLATDAEWQRSKYVPTMEEYMKNSIVTFALGPTILIALYFMGQNLWEDIVKNAEYDELFRLMNTCGRLQNDIQSFERECKDGKLNSVSLLVLDSKDVMSVEEAKEAINESISSCRRELLRLVVREDGVIPKSCKEMFWNLYKTSHVFYSQADGFSSPKEMMGAMNGVIFEPLKTRGN | Involved in the biosynthesis of momilactone A and B phytoalexins. Catalyzes the conversion of syn-copalyl diphosphate to the phytoalexin precursor syn-pimara-7,15-diene.
Subcellular locations: Plastid, Chloroplast
Expressed in roots. |
KSL5_ORYSI | Oryza sativa subsp. indica | MILPMSSACLGQFLRASPRGMIEQFNRAPPLRVSIRGAAGVEKSLGLGRNAGSQQGMQKNQLQDKIRKQLREVQLSPSSYDTAWVAMVPVQGSHQTPRFPQCIEWIMQNQHDDGSWGTNLPGSVVNKDILLCTLACVVALKRWNTGRDHISRGLNFIGKNFWVAMDEQTIAPVGFNITFSGLLNLATGTGLEFPVMQTDIDGIFHMRKIELERDAYGTASSRRAFMAYVSEGLDSLQDWDQVMAYQRKNRSIFNSPSATAATVIHGHNDSALCYLDSLVSKLHGPVPVMYPQNAYSQLCMVDTLEKMGISNNFSCEISDILDMIYRLWIHNEEELMLEMGTCAMAFRLLRMHGYDISSDGMAQFVEQSSFDDSIHGYLNDTKALLELYRSSQIRCLEDDLILQDIGSWSARVLQEKISSKMTHKSEMLGVEYALKFPVYATLERLEQKRNIEQFKTKEQLKIEGFKLLKSGYRGAITHDEILALAVDEFHSSQSVYQQELQDLNSWVAHTRLDELKFARLMPSITYFSAAATMFPSELSEARIAWTQNCILTTTVDDFFDGDGSKEEMENLVKLIKKWDGHGEIGFSSECVEILFYAIYNTSKQIAEKAVPLQKRNVVDHIAESWWFTVRGMLTEAEWRMDKYVPTTVEEYMSAAVDSFAVGPIITSAALFVGPELSEEVFRSEEYIHLMNLANTIGRLLNDMQTYEKEIKMGKVNSIMLHALSHSGGGRGSPEASMEEAKREMRRVLQGSRCDLLRLVTRDGGVVPPPCRKLFWFMSKVLHFVYMEKDGYFTADGMMASANAVILDPLQVTLLPSGLGTL | Involved in the biosynthesis of ent-kaurene diterpenoids natural products . Catalyzes the conversion of ent-copalyl diphosphate to the phytoalexin precursor ent-isokaur-15-ene . |
KTI12_ORYSI | Oryza sativa subsp. indica | MALVVICGQPCSGKSAAAACLAAALCSSTSDLTVRIIDESSLHLGRNDSYKDMVVEKNLRGVLRSEVDRSVSRDSIIVVDSLNNIKGYRYELWCLARASGIRYCVLFCDTEVDHCREWNTKRQEKGEPTYDNNIFDDLVSRFEKPDRRNRWDSPLFELFPSRDGVMESSPVIAEAVSYLTKKVDSKTRDVKVLQPTIATQTARTTEANSLYEMDKATQEVINAIVEAQSCGLGLPVNKISLGPDLPTICLQRSVGLPELRSLRRTFIKLAGQYSLSGPPPPADADSATRMFVDYLNREISS | Elongator complex-associated factor that is not a structural subunit but rather transiently contacts the complex (By similarity). Regulates both meristem activity and organ growth; acts as a positive regulator of adaxial leaf patterning. Required for an early step in synthesis of 5-carbamoylmethyl (ncm5) groups present on uridines (ncm5U) at the wobble position in tRNA (By similarity).
Subcellular locations: Cytoplasm, Nucleus |
KTI12_ORYSJ | Oryza sativa subsp. japonica | MALVVICGQPCSGKSAAAACLAAALCSSTSDLTVRIIDESSLHLGRNDSYKDMVVEKNLRGVLRSEVDRSVSRDSIIVVDSLNNIKGYRYELWCLARASGIRYCVLFCDTEVDHCREWNTKRQEKGEPTYDNNIFDDLVSRFEKPDRRNRWDSPLFELFPSRDGVMESSPVIAEAVSYLTKKVDSKTRDVKVLQPTIATQTARTTEANSLYEMDKATQEVINAIVEAQSCGLGLPVNKISLGPDLPTICLQRSVGLPELRSLRRTFIKLAGQYSLSGPPPPADADSATRMFVDYLNREISS | Elongator complex-associated factor that is not a structural subunit but rather transiently contacts the complex . Regulates both meristem activity and organ growth; acts as a positive regulator of adaxial leaf patterning. Required for an early step in synthesis of 5-carbamoylmethyl (ncm5) groups present on uridines (ncm5U) at the wobble position in tRNA (By similarity).
Subcellular locations: Cytoplasm, Nucleus |
LAC12_ORYSJ | Oryza sativa subsp. japonica | MAAASSVLRCCLLVAALMTLSAMGAEAITRQYLFDVQTTSVTRLCSTKSIVTVNGQYPGPTLFAREGDHVEVTVVNHSPYNMSIHWHGIRQLLSGWADGPSYITQCPIQPGGSYVYRFTITGQRGTLWWHAHISWLRATVHGPMVILPPAGVGYPFPAPHEEVPIMFGEWWNNDTEAVISQALQTGGGPNISDAYTLNGLPGPLYNCSAQDTFKLKVKPGKTYMLRLINAALNDELFFSIANHTLTVVDVDALYVKPFTVDTLIIAPGQTSNVLLTAKPTYPGASYYMLARPYTTTQGTFDNTTVAGVLEYDDPCPTTAAGKIVPIFSPTLPQINDTNAVSNFTAKLRSLASAGYPAAVPQQVDHRFFFTVGLGTHPCAVNGTCQGPNGSRFAASINNVSFVLPATALLQSHFAGKSKGVYASNFPYYPLNPFNYTGTPPNNTNVMNGTKVLVLPYGANVELVMQDTSILGAESHPLHLHGFNFFVVGQGFGNFDPINDPAKFNLYDPVERNTVGVPAGGWVAIRFHADNPGVWFMHCHLEVHMSWGLKMAWLVLDGSRPDQKLPPPPLDLPKC | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC13_ORYSJ | Oryza sativa subsp. japonica | MAAASSVLRCCLLVAALMTLSAMGAEAITRQYLFDVQTTSVTRLCSTKSIVTVNGQYPGPTLFAREGDHVEVTVVNHSPYNMSIHWHGIRQLLSGWADGPSYITQCPIQPGGSYVYRFTITGQRGTLWWHAHISWLRATVHGPMVILPPAGVGYPFPAPHEEVPIMFGEWWNNDTEAVISQALQTGGGPNISDAYTLNGLPGPLYNCSAQDTFKLKVKPGKTYMLRLINAALNDELFFSIANHTLTVVDVDALYVKPFTVDTLIIAPGQTSNVLLTAKPTYPGASYYMLARPYTTTQGTFDNTTVAGVLEYDDPCPTTAAGKIVPIFSPTLPQINDTNAVSNFTAKLRSLASAGYPAAVPQQVDHRFFFTVGLGTHPCAVNGTCQGPNGSRFAASINNVSFVLPATALLQSHFAGKSKGVYASNFPYYPLNPFNYTGTPPNNTNVMNGTKVLVLPYGANVELVMQDTSILGAESHPLHLHGFNFFVVGQGFGNFDPINDPAKFNLYDPVERNTVGVPAGGWVAIRFHADNPGVWFMHCHLEVHMSWGLKMAWLVLDGSRPDQKLPPPPLDLPKC | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC14_ORYSJ | Oryza sativa subsp. japonica | MAPSLGSGSTRILLIVSLLLCLRQQAVVDAAIVEHTFHVGNLTVERLGQRQVITAVNGQFPGPKVEARNGDTLLVRVVNNSPYNITIHWHGVLQRLSAWADGPAMVTQCPILPGSGAGSSYTYRFNVTGQEGTLWWHAHVSFLRATVYGALLIRPRPGVPYPFPAPHAEHTLLLGEWWNASATLVDVERQAFLTGGQPANSVALTINGMPGLSHAHKEMHHLRVARGNTYLLRLVNAALNYQLFFKVAAHNFTVVAVDACYTDPYHTDVIVIAPGQTVDALMHAGAAPGRRYYVAAQVYQSIANATYSATARALLRYDDDAKDAAKTIIMSPRMPVLNDSATAQRFYGSLTGLLRDGKPTVPQRVDTRMVVTYGLAIAPCLPAQTLCNRTRGSLAASMNNVSFQLPATMSLLEASRSRSSGVYTRDFPDRPPVMFDFTNAAAVNRNMSLMVTSKGTRVKALRYNETVEVVLQNTAVLGTENHPLHLHGFNFYVLAQGTGNYYYLIRKKKIRKNLVNPQQRNTIAVPPGGWAVIRFTADNPGVWLMHCHLEAHLPFGLAMAFDVQDGPTPDAMLPPPPNDYPPC | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC15_ORYSJ | Oryza sativa subsp. japonica | MKRCQSSRPTAAVAAVVAAVSMIIVLVSGTAIPSAAAAAAVEHTFVVSQVNMTHLCKEMAFTVVNGQLPGPTIEVTEGDSVTVHVVNKSPYNLTIHWHGVYQLLNCWNDGVPMITQRPIQPNHNFTYRFNVAGQEGTLWWHAHDAFLRGTVHGALIIRPRHGAASYPFPRPHREVPIIIGEWWEKDLPQVDRNMTNGYFDDYSSGSTINGKLGDLFNCSGVLEDGYVLDVEPGKTYLLRIINAALFSEYFLKIAGHRFTVVASDANYLTPYSTDVVVIAPGETLDAIVVADAPPSGRYYIAAQPIQAPPPDTQTPEYATRGTLQYSSNSRNSSAAAMPEMPHQHDTMRSFYFRGNLTAGARLHRHGRRRVPARADESLFVTLGLGSVCRHGGASCKRGGNLKESIVVANVNNVSFHIPAAAATPILEAHYYHRLHAGAGEEEEELAERPPRAYNYTDQALTPFGPEEMRLEATSRAVVTRRFRHGATVDVVFQSTAMLQGDSNPMHLHGHDVFLLAQGIGIYDAARDEGKFNLVNPPRKNTVLVPNLGWAAVRFVADNPGAWLMHCHFEFHLSMGMAAVFIVEDGPTVDTSLPPPPEDF | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC16_ORYSJ | Oryza sativa subsp. japonica | MDRKGIVLGSKLAVFSMILLWHRHGVDQPRNPWSDGPEFITQCPIRPCGNFTYQVILFEEEGTLWWHAHSDFDRATVHGAIVIHPKHGTTFPFNKPDKEIPIILSEWWNDDVENVLDEAKRTGGDQGNTYLLRVINTGLTNDMFFAVAGHCLTVVSIDARYTKPLTVDYIMIAPGQTMDVLLEANRTLGSNSRYYMAARAFITLPVDTIPFNNSTATAIVEYTDSPTARPPGPPEFPLLLPAIKDEDAAMAFVDERMLIDIDVNFLPCDTTNATNKLCKGPQGNQFAASLNNVSFESPAIDVLDAYYYGSGRGVYEEDFPNKPVNAFVNPTGDNGGRPLLTKRGTKVKVVEYGTVVEVVFQDLSSENHPMHLHGFAFYVVGRGSGTFDERRDPATYNLVDPPFQNTVSVPKSSWAAIRFRADNPGVWFMHCHFDRHVVWGMDTVFIVKDGKTPQAQMLPRPPNMPEC | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC17_ORYSJ | Oryza sativa subsp. japonica | MPSRGCSCWLLSLALLCSLAAAKEQYHEFVIRETTVKRLCKSHNIMTVNGQFPGPTLEINEGDSLIINLINRGRYNMTLHWHGVRQMRTGWSDGPEYVTQCPVRPGQSYRYRFTVAAQEGTLWWHAHSSWLRATVYGALLIRPRDGTSYPFDVQPTRELAPILLGEWWDMNPVDVVRAATRTGAAPNISDALTVNAQPGDLYSCSSHDTAVFPVTSGETNLLRFINAALNTELFVSLAGHNMTVVAADASYTKPYTTSLLLLAPGQTTDVLVTFDQPPGRYYLAARAYASAQGVPFDNTTTTAIFDYGAANNASSAAIAMPTLPAYNDTTAATAFTTNLRGLRKAELPSRVDESLFFTVGVGLFNCTNATAQQCGGPNGTRFAASINNVSFVLPSSTSILQAHHHGAPGGVFTADFPANPPVQFDYTAQNVSRALWQPVAGTKVYKLKYGSAVQVVLQGTNIFAGENHPIHLHGYDFYILAEGLGNFDAGADTGKFNVEDPPMRNTVGVPVNGWAVIRFVADNPGVWLMHCHLDVHITWGLAMAFLVDDGVGELQSLEAPPPDLPLC | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC18_ORYSI | Oryza sativa subsp. indica | MEKLSTAASLFGVVVAATALAMAVVGGEAAVVEQTFMVHEMNVTHLCNTTKIYVVNGRFPGPTVDVTEGDTVVVHVINRLPHGLTIHWHGVRQMRSCWADGAGYVTECPIHPGGEKTYRFNVTGQVGTLWWHAHVTCLRATINGAFIIRPRDGKYPFPTPAKDVPIIIGEWWELDLIELDRRMLDGNFDDNPLSATINGKLGDLSNCSGTVEESFVLDVKRGESYLLRVINTALFSEYYFKVAGHTFTVVGADGNYLTPYKTDMVTVAPGEAIDVLMFADAPPAYYHMVALANQPPPPDLQIPQLTSRGLVRYTGAAMDSNNLPMPMPVMPDQHNTMPSYYFRRNLTGLALPEQQQRHRVPAHVDERLLITLGLGSICRGGNTTTCKRGRSPETVVVATMNNVSFHHTNATALLEHYYDGTPEGVYTEDFPVRPPRPFNYTDRELIPAGPLEAALEPTAKAMRLRRFRYNASVEIVFQSTTLLQSDSNPMHLHGYDVFVLAQGLGNFDPKRDVEKFNYHNPQLRNTVQVPRGGWAAVRFLTDNPGMWYLHCHFEFHIIMGMATAFIVEDGPTPETSLPPPPPEFKRCGTNGLSQP | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC18_ORYSJ | Oryza sativa subsp. japonica | MEKLSTAASLFCVVVAATALAMAVVGGEAAVVEQTFMVHEMNVTHLCNTTKIYVVNGRFPGPTVDVTEGDTVVVHVINRLPHGLTIHWHGVRQMRSCWADGAGYVTECPIHPGGEKTYRFNVTGQVGTLWWHAHVTCLRATINGAFIIRPRNGKYPFLTPAKDVPIIIGEWWELDLIELDRRMLDGNFDDNPLSATINGKLGDLSNCSSTVEESFVLDVKRGESYLLRVINTALFSEYYFKVAGHTFTVVGADGNYLTPYKTDMVTVAPGEAIDVLMFTDAPPAYYHMVALANQPPPPDLQIPQLTSRGLIRYAGAAMDSNNLPMPMPVMPDQHNTMPSYYFRRNLTGLALPEQQQRHRVPAHVDERLLITLGLGSICRGGNTTTCKRGRSPETVVVATMNNVSFHHTNATALLEHYYDGRPEGVYTEDFPVRPPRPFNYTDRELIPAGPLEAALEPTAKAMRLRRFRYNASVEIVFQSTTLLQSDSNPMHLHGYDVFVLAQGLGNFDPKRDVEKFNYHNPQLRNTVQVPRGGWAAVRFLADNPGMWYLHCHFEFHIIMGMATAFIVEDGPTPETSLPPPPPEFKRCGTNGLSQP | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC19_ORYSI | Oryza sativa subsp. indica | MEKLSMVTSLLCAITVAVLAVAVVSGEAAVVEHTFVVHEMNATHLCNTTKIYVVNGQFPGPTVDVMEGDTVVVHVINKLPFGLTIHWHGVRQMRSCWADGAGFVTECPIPPGNEHTYRFNVTGQVGTLWWHAHVTCLRATINGAFIVRPRDGKYPFPTPAKDVPIIIGEWWELDLIELDRRMMDGNFDDNPLSATINGKLGDLSNCSRMVEESFILDVKHGESYLLRVINTALFSEYYFRVAGHTFTVVGADGNYLTPFKTDMVTVAPGEAIDVIMVADAPPAHYHMIALANQPPEPDPQIPVFTSRGLVRYAGATANNNGLPVPMPIMPNQHNTMPSYYFHANLTGLAHPERHRVPMHVDERLFVTLGLGSICRGQNTTCKRRRSPETIVVATMNNVSFAHPKTTALLERYYDGTSKGVYTEDFPIRPPRPFNYTNRDLIPPGPLEEALEPTFKATKLKRFKYNTSVEIIFQSTTLMQSDSNPMHLHGYDVFLLAQGLGNFNAKRDVRKFNYHNPQLRNTVQVPRGGWAAIRFVTDNPGMWYLHCHFEFHIIMGMATAFIVEDGPTPETSLPPPPPEFKRCGNNGLSQP | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAC19_ORYSJ | Oryza sativa subsp. japonica | MEKLSMVTSLLCAITVAVLAVAVVSGEAAVVEHTFVVHEMNATHLCNTTKIYVVNGQFPGPTVDVTEGDTVVVHVINKLPFGLTIHWHGVRQMRSCWADGAGFVTECPIPPGNEHTYRFNVTGQVGTLWWHAHVTCLRATINGAFIVRPRDGKYPFPTPAKDVPIIIGEWWELDLIELDRRMMDGNFDDNPLSATINGKLGDLSNCSRMVEESFILDVKHGESYLLRVINTALFSEYYFRVAGHTFTVVGADGNYLTPFKTDMVTVAPGEAIDVIMVADAPPAHYHMIALANQPPEPDPQIPVFTSRGLVRYAGTTANNNGLPVPMPIMPNQHNTMPSYYFHANLTGLAHPERHRVPMHVDERLFVTLGLGSICRGQNTTCKRRRSPETIVVATMNNVSFAHPKTTALLERYYDGTSKGVYTEDFPIRPPRPFNYTNRDLIPPGPLEEALEPTFKATKLKRFKYNTSVEIIFQSTTLMQSDSNPMHLHGYDVFLLAQGLGNFNAKRDVRKFNYHNPQLRNTVQVPRGGWAAIRFVTDNPGMWYLHCHFEFHIIMGMATAFIVEDGPTPETSLPPPPPEFKRCGNNGLSQP | Lignin degradation and detoxification of lignin-derived products.
Subcellular locations: Secreted, Extracellular space, Apoplast |
LAR_DESUN | Desmodium uncinatum | MTVSGAIPSMTKNRTLVVGGTGFIGQFITKASLGFGYPTFLLVRPGPVSPSKAVIIKTFQDKGAKVIYGVINDKECMEKILKEYEIDVVISLVGGARLLDQLTLLEAIKSVKTIKRFLPSEFGHDVDRTDPVEPGLTMYKEKRLVRRAVEEYGIPFTNICCNSIASWPYYDNCHPSQVPPPMDQFQIYGDGNTKAYFIDGNDIGKFTMKTIDDIRTLNKNVHFRPSSNCYSINELASLWEKKIGRTLPRFTVTADKLLAHAAENIIPESIVSSFTHDIFINGCQVNFSIDEHSDVEIDTLYPDEKFRSLDDCYEDFVPMVHDKIHAGKSGEIKIKDGKPLVQTGTIEEINKDIKTLVETQPNEEIKKDMKALVEAVPISAMG | Catalyzes the synthesis of catechin from 3,4-cis-leucocyanidin. Also synthesizes afzelechin and gallocatechin. |
LDL1_ORYSJ | Oryza sativa subsp. japonica | MEEGSEAQPPLQPEAVSAEASEPPPPVPMDQDEGQAAAAEAMEGEAEGAAAAAGTIEGEAGYAAADADPMEDEAADEAGAAEPMEDDPPTSSAPSATAAVDDSTIARKRRRRKKQFPGMIPTAGVRVLRAAASAPSAAHLNGVPRRRGRPPTSSSLRLARELDAEALIALAAGFPADSLSEDEVAAAVLPRIGGVDQTNYLVVRNHVLALWRSNPLSPVASNAALASIRAEHAHLVAAAHSFLSDHAYINFGLAPSVISLPPCPPPSLPPPSVLIVGAGFAGLAAARHLMSLGFKVAIVEGRLRPGGRVFTKSMRSTAAEYPDIAAAADLGGSVLTGINGNPLGVIARQLGFPLHKVRDKCPLYLPDGRPVDPDMDARVEAAFNQLLDKVCQLRQVVADSIPHGVDVSLGMALEAFRAAHGVAAEREERMLLDWHLANLEYANAAPLVDLSMAFWDQDDPYEMGGDHCFIPGGNSRFVRALADGIPIFYGQNVRRIQYGCDGAMVYTDKQTFRGDMVLCTVPLGVLKKGNIQFVPELPAQKREAIERLGFGLLNKVVLLFPYDFWDGRIDTFGHLTEDSGQRGEFFLFYSYSSVSGGPLLIALVAGESAIEFEKTSPAENVEKVLETLRKIFSPKGIEVPKPLQAICTRWGTDKFTYGSYSYVAIGSSGDDYDILAESVCDRVFFAGEATNRRYPATMHGALLSGYREAANIVRAARRRAKKVDSPKKMDVNNEVKYEVKVDNIDLDDLFRTPDAAFGGFSVLHDPSTSEPDSISLLRVGIGARKLGSGSLFLYGLIMRKNVANLAAMEGDEQRLSTLYRDFGTKLVGLDGLGDSGSSLISRIKAAARK | Probable histone demethylase. |
LDL2_ORYSJ | Oryza sativa subsp. japonica | MSSSSRRPARRAALTARSSYDESLVDAELESYLGNARSRRISRLRRLSADERQRETETEALIALSLGFPIDELLPAERPLLPAPVAAAPNDYIVVRNHILASWRADPRVPLPRSRVQETVAASYDNLVAVAHGFLAREGHINFGVSAAFPASPPPDAPQRLAASVLVVGAGLAGLAAARQLLRFGLRVLVLEGRARPGGRVYTTHLGGDQAAVELGGSVITGIHTNPLGVLARQLGIPLHKVRDSCPLYHHDGRTVDMKLDRSMDLVFNTLLEHATRLREYLKKAAEGISLGEGIERLRRFYKVAKSVEEREVLDWHLANLEFSNAGCLSELSLAHWDQDDQYEMGGDHCFLAGGNARLVHALCDGVPVLYEKTVKRIEHGEDGVSITVEGGQVFKADMALCTAPLGVLKSRSIIFEPELPERKLEAIQRLGFGLLNKVAMVFPHVFWDEEIDTFGCLNKERSKRGEFFLFYSYHTVSGGAVLIALVAGEAALEFEKVDPAVALHRVLGILKGIYGPKGVTVPDPIQSCCTRWGSDPLCSGSYSHIRVGSSGTDYDILAESVNDRLFFAGEATNRAYPATMHGALLSGLREASKILHASESRLNSDYKKYALQKSIRLINNVLDDLFMEPDLECGRFSFVFSYITPEEEQAPGLARITLEKPLLLPSKKRKVKGNQKDQDPVAEKIDQEVFYLYATVSQEQATELLECDNDKSRIAVLCKDLGVKLMGYDSTYDVCSHLISSISRAQKARKRLQGPKSLKTGL | Probable histone demethylase. |
LDL3_ORYSI | Oryza sativa subsp. indica | MSDQPPPYTPLPLLSSFPPNPYPDQTPDPASTPTLVLPNPAFPNKRKRTGFRRKLPSGSPAAPVAVAASPSAQPPPRASAADDIIVINREPTAEAVTALTAGFPADSLTDEEIEAGVVSDVGGIEQVNYILIRNHLLTRWRETFNSWLAKESFATLIPPHCDHLLNAAYSFLVSHGHINFGVAPAIKERIPKEPTRHNTVIVVGAGLAGLAAARQLVAFGFKVVVLEGRKRCGGRVYTKKMEGGGRSAAGDLGGSVLTGTFGNPLGIVAKQLGLPMHKIRDKCPLYRPDGSPVDPEVDKKVEGTFNKLLDKSSLLRASMGDVAMDVSLGAALETLRQTDGDLSTDQEMNLFNWHLANLEYANAGLLSKLSLAFWDQDDPYDMGGDHCFLPGGNGRLVQALAENVPIVYERTVHTIRNGGDGVQVVVNGGQVYEGDMALCTVPLGVLKNGGVKFVPELPQRKLDSIKRLGFGLLNKVAMLFPHVFWSTDLDTFGHLTEDPSHRGEFFLFYSYATVAGGPLLMALVAGEAAHNFETTPPTDAVSSVLKILRGIYEPQGIEVPDPLQSVCTRWGTDSFSLGSYSHVAVGASGDDYDILAESVGDGRLFFAGEATTRRYPATMHGAFISGLREAANITLHANARAAKSKVEKGPSTNTQACAALLMDLFRQPDLEFGSFSVIFGGQASDPKSPAILKVELGGPRKKGATEGGKADQHHSNKLLFQQLQSHFNQQQQLYVYTLLSRQQAMELREVRGGDEMRLHYLCEKLGVKLVGRKGLGPGADAVIASIKAERNSSRTKTRPSKLKIGIPKSKS | Probable histone demethylase. |
LDL3_ORYSJ | Oryza sativa subsp. japonica | MSDQPPPYTPLPLLSSFPPNPYPDQTPDPASTPTLVLPNPAFPNKRKRTGFRRKLPSGSPAAPVAVAASPSAQPPPRASAADDIIVINREPTAEAVTALTAGFPADSLTDEEIEAGVVSDVGGIEQVNYILIRNHLLTRWRETFNSWLAKESFATLIPPHCDHLLNAAYSFLVSHGHINFGVAPAIKERIPKEPTRHNTVIVVGAGLAGLAAARQLVAFGFKVVVLEGRKRCGGRVYTKKMEGGGRSAAGDLGGSVLTGTFGNPLGIVAKQLGLPMHKIRDKCPLYRPDGSPVDPEVDKKVEGTFNKLLDKSSLLRASMGDVAMDVSLGAALETLRQTDGDLSTDQEMNLFNWHLANLEYANAGLLSKLSLAFWDQDDPYDMVGDHCFLPGGNGRLVQSLAENVPIVYERTVHTIRYGGDGVQVVVNGGQVYEGDMALCTVPLGVLKNGGVKFVPELPQRKLDSIKRLGFGLLNKVAMLFPHVFWSTDLDTFGHLTEDPSHRGEFFLFYSYATVAGGPLLMALVAGEAAHNFETTPPTDAVSSVLKILRGIYEPQGIEVPDPLQSVCTRWGTDSFSLGSYSHVAVGASGDDYDILAESVGDGRLFFAGEATTRRYPATMHGAFISGLREAANITLHANARAAKSKVEKGPSTNTQACAALLMDLFRQPDLEFGSFSVIFGGQASDPKSPAILKVELGGPRKKGATEGGKADQHHSNKLLFQQLQSHFNQQQQLYVYTLLSRQQAMELREVRGGDEMRLHYLCEKLGVKLVGRKGLGPGADAVIASIKAERNSSRTKTRPSKLKIGIPKSKS | Probable histone demethylase. |
LEGRE_SOYBN | Glycine max | MAMANLARRKGYAVVLSSRSSLCLTRWRGFASGSDENDVVVIGGGPGGYVAAIKAAQLGLKTTCIEKRGTLGGTCLNVGCIPSKALLHSSHMYHEAKHAFANHGVKFSSVEVALPAMMGQKDKAVSNLTQGIDGLFQKNKVTYVKGYGKLVSPSEISVDTTEGENTVVKGKHIIIATGSDVKSLPGVTIDEKKIVSSTGALALSEIPKKLVVIGAGYIGLEMGSVWGRIGSEVTVVEFASEIVPTMDADIRKQFQRSLEKQGMKFKLKTKVVGVDTSGDGVKLTVEPSAGGEQTIIEADVVLVSAGRTPFTSGLNLDKIGVETDKLGRILVNERFSTNVSGVYAIGDVIPGPMLAHKAEEDGVACVEYLTGKVGHVDYDKVPGVVYTNPEVASVGKTEEQVKETGVEYRVGKFPFLANSRAKAIDNAEGLVKIIAEKETDKILGVHIMAPNAGELIHEAAIALQYDASSEDIARVCHAHPTMSEAVKEAAMATYDKPHSHLKSWLLLSSLVFIFVQEFTMTWR | Reduces ferric leghemoglobin (Lb) to ferrous Lb.
Subcellular locations: Mitochondrion
Widely expressed. Expressed at higher level in leaf and nodules. |
LEGRE_VIGUN | Vigna unguiculata | MAMASLARRKAYAVVSSSRSSVFLTSLRGFASGSDENDVVVIGGGPGGYVAAIKASQLGLKTTCIEKRGTLGGTCLNVGCIPSKALLHSSHMYHEAKHSFANHGIKLSSVEVDLAGMMAQKDKAVSNLTKGIEGLFKKNKVNYVKGYGKFVSPSEVSVDTIDGGNTVVKGKHIIIATGSDVKSLPGVTIDEKKIVSSTGALALTEIPKKLVVIGAGYIGLEMGSVWGRLGSEVTVVEFASDIVPTMDAEVRKQFQRSLEKQGMKFQLKTKVVGVDTSGDGVKLTLEPAAGGDQTILETDVVLVSAGRTPFTAGLGLDKIGVETDKIRRILVNERFTTNVSGVYAIGDVIPGPMLAHKAEEDGVACVEFIAGKVGHVDYDKVPGVVYTTPEVAYVGKTEEQVKALGVEYRVGKFPFMANSRAKAIDNAEGLVKILAEKETDKILGVHIMAPNAGELIHEAAIALQYDASSEDIARVCHAHPTMSEAVKEAAMATYDKPHSHMKSWLLLHSLLFIFVQQFTMTWR | Reduces ferric leghemoglobin (Lb) to ferrous Lb.
Subcellular locations: Mitochondrion |
LEGU_CANEN | Canavalia ensiformis | MVMMLVMLSLHGTAARLNRREWDSVIQLPTEPVDDEVGTRWAVLVAGSNGYGNYRHQADVCHAYQLLIKGGVKEENIVVFMYDDIAYNAMNPRPGVIINHPQGPDVYAGVPKDYTGEDVTPENLYAVILGDKSKVKGGSGKVINSNPEDRIFIFYSDHGGPGVLGMPNAPFVYAMDFIDVLKKKHASGGYKEMVIYIEACESGSIFEGIMPKDLNIYVTTASNAQENSFGTYCPGMNPPPPEEYVTCLGDLYSVSWMEDSETHNLKRETVQQQYQSVRKRTSNSNSYRFGSHVMQYGDTNITAEKLYLYHGFDPATVNFPPHNGNLEAKMEVVNQRDAELLFMWQMYQRSNHQPEKKTHILEQITETVKHRNHLDGSVELIGVLLYGPGKSSSVLHSVRAPGLPLVDDWTCLKSMVRVFETHCGSLTQYGMKHMRAFGNVCNSGVSKASMEEACKAACGGYDAGLLYPSNTGYSA | Asparaginyl endopeptidase able to cleave almost all peptide bonds on the carboxyl side of Asn residues, except at the NH2 terminus or second position or with N-glycosylated Asn . Responsible for the maturation (circular permutation) of concanavalin A from its precursor, by performing both cleavage and cleavage-coupled transpeptidation to form conA (, ). |
LEG_CICAR | Cicer arietinum | MAKLLALSLSFCFLLFGTCFALRDQPQQNECQLEHLNALKPDNRIKSEGGLIETWNPSNKQFACAGVALSRATLQPNSLLQTFLHQRSPEIFIQQGNGYFGMVFPGCVETFEEPRESEQGEGSKFSDSHQKVNRFREGDIIAVPTGVVFWMFNDQDTPVIAVSLIDTSSFQNQLDQMPRRFYLAGNHEQEFLRYQQEGSEEEENEGGNIFSGFKRDFLEDALNVNRRIVNKLQGRNEDEEKGAIVKVKGGLSITTPPEKEPRQKRGSRQEEDEDEDEKRQPHRHSRQDEDEDEKRQPHHHSRGGSKSQRDNGFEETICTARLHQNIGSSSSPDIYNPQAGRIKTVTSFDLQALRFLKLSAEFGSLHKNAMFVPHYNLNANSILYALKGRARLLYALNCKGNSVFDGELEAGRALIVPQNFAIAAKSLSDRFSYVAFKTNDRALINVCQKKLLQLLSIWKEMRPGSSSSTAPFHFLFHPAVTQTTKQQLDLVPNQYE | Seed storage protein (By similarity). Alpha-amylase inhibitor. |
LEU1_SOYBN | Glycine max | MPTKTSTPSSQSPKLSHLRPQYIPNHIPDSSYVRILDTTLRDGEQSPGATMTAKEKLDIARQLVKLGVDIIQPGFPSASNSDFMAVKMIAQEVGNAVDDDGYVPVIAGFCRCVEKDISTAWEAVKYAKRPRLCTSIATSPIHMEHKLRKSKDQVIQIARDMVKFARSLGCNDIQFGAEDATRSDREFLYEILGVVIEAGATTVNIADTVGIVMPLELGKLIVDIKDNTPGIANVIISTHCHNDLGLATANTIEGARTGARQLEVTINGIGERAGNASLEEVVMALASKGDHALNGLYTRINTRHILETSKMVEEYSGMHLQPHKPLVGANAFVHASGIHQDGMLKHKGTYETISPEEIGHKRTTRIGIVLGKLSGSQALRKRLEELGYDLKEDEVDSVFWQFKAMAEKKKVVTDVDLKALVSYKAFHAESIWKLGDLQVTCGTIGLSTATVKLVNIDGSTHVACSIGIGAVDSTYKAINLIVKEPTKLLDYSLNSVTEGIGVNVTARVVICRENNHTSTYAFTEDANYPTFSGIAAEMDVVVSTVKAYLVALNKLLRWKESFRCA | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity). May play an important role in symbiotic nitrogen fixation (Probable).
Exclusively expressed in mature nodules. |
LFL1_ORYSJ | Oryza sativa subsp. japonica | MRGEERWQEQPALASHPSRATLRPRGWPRLGLAPTGVGSSCPPAPASELARHLARRAPVSASPPVLPPIKDQGARPPTLAASAAAASSPPPPPPPPIPPLPPSTSTSAARPTDMAGVTSKRRSSSASTSSSSGDGAAVSDRPRGVTRKRRSGGRCPRPAASLRPAAPRPSSHHTAGLRVILQKELRYSDVSQLGRIVLPKKEAEAYLPILTSKDGKKSLCMHDLQNAQLWTFKYRYWPNNKSRMYVLENTGDYVRTHDLQLGDSIVIYKDDENNRFVIGAKKAGDQQAATVPQVDEHISTLFPIFPIAQVDDYLSPMAPQVDISAFVPHADENHEIFDGILNSLPEIPVANVRYSDFFDPFDDGMDMANTLNANANQSASLHVTDDKSGHSLIPNPKSGPHM | Transcription repressor involved in flowering time regulation. Represses the flowering activator EHD1 by binding specifically to the DNA sequence 5'-CATGCATG-3 of its promoter.
Subcellular locations: Nucleus
Expressed in anthers, pollen grains and young developing embryos. |
LFR_ORYSJ | Oryza sativa subsp. japonica | MSHVRSAPAGKSGGGGGSTPAKRGRPFGSTTGSGAAAAAAAAAIGDAAAPAALVGPSLQVLTALSDQNNKRIVLALQSGLKSEILWALNALTVLSFKEKDDLRRDTTPLAKVPGLLDALLQVIDDWRDIAMPKDHTKPPRVRTLGVNTTLSGFGHENVEKVYSDTTTPSDDQTKTADSTVTKKRSAGFLFDEEGLFNVDDEGRTEKQQCAVAASNIIRNFSFMPENETVMVQHRHCLETVFQCLEDQNTEDDELITNMLETLVNLAPVLDLRIFSSSKPSFIKITEKRAVQAIMGMLASSIRVWHCAAAELIGRLIINPDNEPFLLPAIPQIYKRLVDLLSVPAVDAQAAAISALYNVAEVNMDFRLKLASERWAVDRLLKVVKTPHPVPEVCRKASMIVESLVSEPQNRMHLLVHENTFAEILTSEGKYSDTFARILYELTARPSNKVTAGQAIWGNIN | Plays critical roles in both embryo and endosperm development . Required for free nuclei division and cellularization in early endosperm development, by preventing premature cell death in the endosperm . Involved in the regulation of pattern formation and organ differentiation during embryogenesis, by regulating genes involved in the early stages of seed development .
Subcellular locations: Nucleus
Expressed at low levels in coleoptiles, leaf tongues, mature leaves and nodes during the vegetative phase . Highly expressed in reproductive tissues such as young panicles, early developing seeds, embryos and endosperms . |
LIAS1_PEA | Pisum sativum | MMYSRFRTVAGNLNCAAKRLSSSSTTTTTTSAPSELQQNLAALRARLAMESPSLSDFISLKSDNAYSVEVGTKKKPLPKPKWMKESIPGGEKYVQIKKKLRELKLHTVCEEAKCPNLGECWSGGETGTATATIMILGDTCTRGCRFCNVKTSRTPPPPDPDEPTNVAEAIASWGLDYVVITSVDRDDLPDQGSGHFTETVQKLKALKPSTLIEALVPDFRGNAECVEKVSKSGLDVFAHNIETVEELQSAVRDHRANFKQSLDVLMMAKEYAPAGTLTKTSIMLGCGETPDQIVKTMEKVRAAGVDVMTFGQYMRPSKRHMPVSEYITPEAFEKYQTLGMEMGFRYVASGPMVRSSYKAGEFYIKSMIDSDRAASS | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives.
Subcellular locations: Mitochondrion |
LIAS2_PEA | Pisum sativum | MMYSRFRTVAGNLNCAAKRLSSSSTTTTTTSAPSELQQNLAALRARLAMESPSLSDFISLKSDNAYSVEVGTKKKPLPKPKWMKESIPGGEKYVQIKKKLRELKLHTVCEEAKCPNLGECWSGGETGTATATIMILGDTCTRGCRFCNVKTSRTPPPPDPDEPTNVAEAIASWGLDYVVITSVDRDDLPDQGSGHFTETVQKLKALKPSMLIEALVPDFRGNAECVEKVSKSGLDVFAHNIETVEELQSAVRDHRANFKQSLDVLMMAKEYAPAGTLTKTSIMLGCGETPDQIVKTMEKVRAAGVDVMTFGQHMRPSKRHMPVSEYITPEAFEKYQTLGMEMGFRYVASGPMVRSSYKAGEFYIKSMIDSDRAASS | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives.
Subcellular locations: Mitochondrion |
LO917_ORYSI | Oryza sativa subsp. indica | MEKSPPETAAAAAEVAARFRSLVDTGDIGAIRQTQHLILGRLQDSNAVLTHFNEYSEQCFAEVSNDFASKTRLLKSMKDDLDHIFLKLRSMKSRLAATYPDAFPDGAMAKTMDQRPDLESPLD | Contributes, together with ILI5/BUL1 and BC1, to the promotion of leaf inclination and grain size by modulating cell elongation.
Subcellular locations: Nucleus, Cytoplasm |
LO917_ORYSJ | Oryza sativa subsp. japonica | MEKSPPETAAAAAEVAARFRSLVDTGDIGAIRQTQHLILGRLQDSNAVLTHFNEYSEQCFAEVSNDFASKTRLLKSMKDDLDHIFLKLRSMKSRLAATYPDAFPDGAMAKTMDQRPDLESPLD | Contributes, together with ILI5/BUL1 and BC1, to the promotion of leaf inclination and grain size by modulating cell elongation.
Subcellular locations: Nucleus, Cytoplasm
Mostly expressed in leaves blades and leaves sheaths and, to a lower extent, in seedings, roots, collars and panicles. |
LONM_ORYSI | Oryza sativa subsp. indica | MLRAAAAAAAVFPSRFAAAPAVAAVEEVRSPLLRVLGALRGGRVSTLGRRARFCSNSAGSDSEAAAAEAKAEDAVAAEGEADGKASSAIVPTVLRPEDCLSVIALPLPHRPLFPGFYMPIYVKDQKLLQALVENRKRSIPYAGAFLVKDEEGTDPNIVTSSDSDKSIDDLKGKELLQRLNEVGTLAQITSIQGDQVVLLGHRRLKITEMVQEDPLTVKVDHLKEKPYDKDDDVIKATSFEVISTLREVLKASSLWKDHVQTYTQHMGDFNYPRLADFGAAISGANKFLCQEVLEELDVYKRLKLTLELVKKEMEISKLQQSIAKAIEEKISGDQRRYLLNEQLKAIKKELGLETDDKTALSAKFRERIEAKKEKCPAHVLQVIEEELTKLQLLEASSSEFNVTRNYLDWLTVLPWGNYSDENFDVHHAQQILDEDHYGLSDVKERILEFIAVGKLRGTSQGKIICLSGPPGVGKTSIGRSIARALNRKFYRFSVGGLADVAEIKGHRRTYVGAMPGKMVQCLKSVGTANPLVLIDEIDKLGRGHSGDPASALLELLDPEQNVNFLDHYLDVPIDLSKVLFVCTANVIEMIPNPLLDRMEIIAIAGYITDEKMHIARDYLEKNTREACGIKPEQAEVTDAALLALIESYCREAGVRNLQKQIEKIYRKIALQLVRQGVSNEPTQEAAIVTASEEPNGGDSANKLKDETMEDPATENAAMTNADTASKEASELDLLKRTVDHDVHPAETPKEAVLTDSALSTDKLCTPEGNKDMEGAKEESADKAVEKVVIDSSNLGDYVGKPVFQAERIYEQTPVGVVMGLAWTAMGGSTLYIETTKVEEGDGKGALVLTGQLGDVMKESAQIAHTVGRAILLDKEPENLFFANSKVHLHVPAGSTPKDGPSAGCTMITSMLSLAMGKPVKKDLAMTGEVTLTGRILPIGGVKEKTIAARRSAVKTIVFPAANKRDFDELAPNVKEGLEVHFVDTYNEIFDIAFQSETQTETS | ATP-dependent serine protease that mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides as well as certain short-lived regulatory proteins in the mitochondrial matrix. May also have a chaperone function in the assembly of inner membrane protein complexes. Participates in the regulation of mitochondrial gene expression and in the maintenance of the integrity of the mitochondrial genome. Binds to mitochondrial DNA in a site-specific manner.
Subcellular locations: Mitochondrion matrix |
LONM_ORYSJ | Oryza sativa subsp. japonica | MLRAAAAAAAVFPSRFAAAPAVAAVEEVRSPLLRVLGALRGGRVSTLGRRARFCSNSAGSDSEAAAAEAKAEDAVAAEGEADGKASSAIVPTVLRPEDCLSVIALPLPHRPLFPGFYMPIYVKDQKLLQALVENRKRSIPYAGAFLVKDEEGTDPNIVTSSDSDKSIDDLKGKELLQRLNEVGTLAQITSIQGDQVVLLGHRRLKITEMVQEDPLTVKVDHLKEKPYDKDDDVIKATSFEVISTLREVLKASSLWKDHVQTYTQHMGDFNYPRLADFGAAISGANKFLCQEVLEELDVYKRLKLTLELVKKEMEISKLQQSIAKAIEEKISGDQRRYLLNEQLKAIKKELGLETDDKTALSAKFRERIEAKKEKCPAHVLQVIEEELTKLQLLEASSSEFNVTRNYLDWLTVLPWGNYSDENFDVHHAQQILDEDHYGLSDVKERILEFIAVGKLRGTSQGKIICLSGPPGVGKTSIGRSIARALNRKFYRFSVGGLADVAEIKGHRRTYVGAMPGKMVQCLKSVGTANPLVLIDEIDKLGRGHSGDPASALLELLDPEQNVNFLDHYLDVPIDLSKVLFVCTANVIEMIPNPLLDRMEIIAIAGYITDEKMHIARDYLEKNTREACGIKPEQAEVTDAALLALIESYCREAGVRNLQKQIEKIYRKIALQLVRQGVSNEPTQEAAIVTASEEPNGGDSANKLKDETMEDPATENAAMTNADTASKEASELDLLNRTVDHDVHPAETPKEAVLTDSALSTDKLCTPEGNKDMEGAKEESADKAVEKVVIDSSNLGDYVGKPVFQAERIYEQTPVGVVMGLAWTAMGGSTLYIETTKVEEGDGKGALVMTGQLGDVMKESAQIAHTVGRAILLDKEPENLFFANSKVHLHVPAGSTPKDGPSAGCTMITSMLSLAMGKPVKKDLAMTGEVTLTGRILPIGGVKEKTIAARRSAVKTIVFPAANKRDFDELAPNVKEGLEVHFVDTYNEIFDIAFQSETQTETS | ATP-dependent serine protease that mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides as well as certain short-lived regulatory proteins in the mitochondrial matrix. May also have a chaperone function in the assembly of inner membrane protein complexes. Participates in the regulation of mitochondrial gene expression and in the maintenance of the integrity of the mitochondrial genome. Binds to mitochondrial DNA in a site-specific manner.
Subcellular locations: Mitochondrion matrix |
LPAT_MAIZE | Zea mays | MAIPLVLVVLPLGLLFLLSGLIVNAIQAVLFVTIRPFSKSFYRRINRFLAELLWLQLVWVVDWWAGVKVQLHADEETYRSMGKEHALIISNHRSDIDWLIGWILAQRSGCLGSTLAVMKKSSKFLPVIGWSMWFAEYLFLERSWAKDEKTLKWGLQRLKDFPRPFWLALFVEGTRFTPAKLLAAQEYAASQGLPAPRNVLIPRTKGFVSAVSIMRDFVPAIYDTTVIVPKDSPQPTMLRILKGQSSVIHVRMKRHAMSEMPKSDEDVSKWCKDIFVAKDALLDKHLATGTFDEEIRPIGRPVKSLLVTLFWSCLLLFGAIEFFKWTQLLSTWRGVAFTAAGMALVTGVMHVFIMFSQAERSSSARAARNRVKKE | Converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating acyl moiety at the 2 position.
Subcellular locations: Membrane |
LT01_HORVU | Hordeum vulgare | MGSATVLEVILAIILPPVGVFLRYKLGVEFWICLLLTILGYIPGIIYAVYVLVV | Subcellular locations: Membrane
Expressed in shoot meristems, mature leaves and roots. |