# Copyright 2021 DeepMind Technologies Limited
#
# Licensed under the Apache License, Version 2.0 (the "License");
# you may not use this file except in compliance with the License.
# You may obtain a copy of the License at
#
#      http://www.apache.org/licenses/LICENSE-2.0
#
# Unless required by applicable law or agreed to in writing, software
# distributed under the License is distributed on an "AS IS" BASIS,
# WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
# See the License for the specific language governing permissions and
# limitations under the License.

"""Protein data type.
Adapted from original code by alexechu.
"""
import dataclasses
import io
from typing import Any, Mapping, Optional
from core import residue_constants
from Bio.PDB import PDBParser
import numpy as np

FeatureDict = Mapping[str, np.ndarray]
ModelOutput = Mapping[str, Any]  # Is a nested dict.

# Complete sequence of chain IDs supported by the PDB format.
PDB_CHAIN_IDS = "ABCDEFGHIJKLMNOPQRSTUVWXYZabcdefghijklmnopqrstuvwxyz0123456789"
PDB_MAX_CHAINS = len(PDB_CHAIN_IDS)  # := 62.


@dataclasses.dataclass(frozen=True)
class Protein:
    """Protein structure representation."""

    # Cartesian coordinates of atoms in angstroms. The atom types correspond to
    # residue_constants.atom_types, i.e. the first three are N, CA, CB.
    atom_positions: np.ndarray  # [num_res, num_atom_type, 3]

    # Amino-acid type for each residue represented as an integer between 0 and
    # 20, where 20 is 'X'.
    aatype: np.ndarray  # [num_res]

    # Binary float mask to indicate presence of a particular atom. 1.0 if an atom
    # is present and 0.0 if not. This should be used for loss masking.
    atom_mask: np.ndarray  # [num_res, num_atom_type]

    # Residue index as used in PDB. It is not necessarily continuous or 0-indexed.
    residue_index: np.ndarray  # [num_res]

    # 0-indexed number corresponding to the chain in the protein that this residue
    # belongs to.
    chain_index: np.ndarray  # [num_res]

    # B-factors, or temperature factors, of each residue (in sq. angstroms units),
    # representing the displacement of the residue from its ground truth mean
    # value.
    b_factors: np.ndarray  # [num_res, num_atom_type]

    def __post_init__(self):
        if len(np.unique(self.chain_index)) > PDB_MAX_CHAINS:
            raise ValueError(
                f"Cannot build an instance with more than {PDB_MAX_CHAINS} chains "
                "because these cannot be written to PDB format."
            )


def from_pdb_string(
    pdb_str: str, chain_id: Optional[str] = None, protein_only: bool = False
) -> Protein:
    """Takes a PDB string and constructs a Protein object.

    WARNING: All non-standard residue types will be converted into UNK. All
      non-standard atoms will be ignored.

    Args:
      pdb_str: The contents of the pdb file
      chain_id: If chain_id is specified (e.g. A), then only that chain
        is parsed. Otherwise all chains are parsed.

    Returns:
      A new `Protein` parsed from the pdb contents.
    """
    pdb_fh = io.StringIO(pdb_str)
    parser = PDBParser(QUIET=True)
    structure = parser.get_structure("none", pdb_fh)
    models = list(structure.get_models())
    if len(models) != 1:
        raise ValueError(
            f"Only single model PDBs are supported. Found {len(models)} models."
        )
    model = models[0]

    atom_positions = []
    aatype = []
    atom_mask = []
    residue_index = []
    chain_ids = []
    b_factors = []

    for chain in model:
        if chain_id is not None and chain.id != chain_id:
            continue
        for res in chain:
            if protein_only and res.id[0] != " ":
                continue
            if res.id[2] != " ":
                pass
                # raise ValueError(
                #     f"PDB contains an insertion code at chain {chain.id} and residue "
                #     f"index {res.id[1]}. These are not supported."
                # )
            res_shortname = residue_constants.restype_3to1.get(res.resname, "X")
            restype_idx = residue_constants.restype_order.get(
                res_shortname, residue_constants.restype_num
            )
            pos = np.zeros((residue_constants.atom_type_num, 3))
            mask = np.zeros((residue_constants.atom_type_num,))
            res_b_factors = np.zeros((residue_constants.atom_type_num,))
            for atom in res:
                if atom.name not in residue_constants.atom_types:
                    continue
                pos[residue_constants.atom_order[atom.name]] = atom.coord
                mask[residue_constants.atom_order[atom.name]] = 1.0
                res_b_factors[residue_constants.atom_order[atom.name]] = atom.bfactor
            if np.sum(mask) < 0.5:
                # If no known atom positions are reported for the residue then skip it.
                continue
            aatype.append(restype_idx)
            atom_positions.append(pos)
            atom_mask.append(mask)
            residue_index.append(res.id[1])
            chain_ids.append(chain.id)
            b_factors.append(res_b_factors)

    # Chain IDs are usually characters so map these to ints.
    unique_chain_ids = np.unique(chain_ids)
    chain_id_mapping = {cid: n for n, cid in enumerate(unique_chain_ids)}
    chain_index = np.array([chain_id_mapping[cid] for cid in chain_ids])

    return Protein(
        atom_positions=np.array(atom_positions),
        atom_mask=np.array(atom_mask),
        aatype=np.array(aatype),
        residue_index=np.array(residue_index),
        chain_index=chain_index,
        b_factors=np.array(b_factors),
    )


def _chain_end(atom_index, end_resname, chain_name, residue_index) -> str:
    chain_end = "TER"
    return (
        f"{chain_end:<6}{atom_index:>5}      {end_resname:>3} "
        f"{chain_name:>1}{residue_index:>4}"
    )


def are_atoms_bonded(res3name, atom1_name, atom2_name):
    lookup_table = residue_constants.standard_residue_bonds
    for bond in lookup_table[res3name]:
        if bond.atom1_name == atom1_name and bond.atom2_name == atom2_name:
            return True
        elif bond.atom1_name == atom2_name and bond.atom2_name == atom1_name:
            return True
    return False


def to_pdb(prot: Protein, conect=False) -> str:
    """Converts a `Protein` instance to a PDB string.

    Args:
      prot: The protein to convert to PDB.

    Returns:
      PDB string.
    """
    restypes = residue_constants.restypes + ["X"]
    res_1to3 = lambda r: residue_constants.restype_1to3.get(restypes[r], "UNK")
    atom_types = residue_constants.atom_types

    pdb_lines = []

    atom_mask = prot.atom_mask
    aatype = prot.aatype
    atom_positions = prot.atom_positions
    residue_index = prot.residue_index.astype(np.int32)
    chain_index = prot.chain_index.astype(np.int32)
    b_factors = prot.b_factors

    if np.any(aatype > residue_constants.restype_num):
        raise ValueError("Invalid aatypes.")

    # Construct a mapping from chain integer indices to chain ID strings.
    chain_ids = {}
    for i in np.unique(chain_index):  # np.unique gives sorted output.
        if i >= PDB_MAX_CHAINS:
            raise ValueError(
                f"The PDB format supports at most {PDB_MAX_CHAINS} chains."
            )
        chain_ids[i] = PDB_CHAIN_IDS[i]

    pdb_lines.append("MODEL     1")
    atom_index = 1
    last_chain_index = chain_index[0]
    conect_lines = []
    # Add all atom sites.
    for i in range(aatype.shape[0]):
        # Close the previous chain if in a multichain PDB.
        if last_chain_index != chain_index[i]:
            pdb_lines.append(
                _chain_end(
                    atom_index,
                    res_1to3(aatype[i - 1]),
                    chain_ids[chain_index[i - 1]],
                    residue_index[i - 1],
                )
            )
            last_chain_index = chain_index[i]
            atom_index += 1  # Atom index increases at the TER symbol.

        res_name_3 = res_1to3(aatype[i])
        atoms_appended_for_res = []
        for atom_name, pos, mask, b_factor in zip(
            atom_types, atom_positions[i], atom_mask[i], b_factors[i]
        ):
            if mask < 0.5:
                continue

            record_type = "ATOM"
            name = atom_name if len(atom_name) == 4 else f" {atom_name}"
            alt_loc = ""
            insertion_code = ""
            occupancy = 1.00
            element = atom_name[0]  # Protein supports only C, N, O, S, this works.
            charge = ""
            # PDB is a columnar format, every space matters here!
            atom_line = (
                f"{record_type:<6}{atom_index:>5} {name:<4}{alt_loc:>1}"
                f"{res_name_3:>3} {chain_ids[chain_index[i]]:>1}"
                f"{residue_index[i]:>4}{insertion_code:>1}   "
                f"{pos[0]:>8.3f}{pos[1]:>8.3f}{pos[2]:>8.3f}"
                f"{occupancy:>6.2f}{b_factor:>6.2f}          "
                f"{element:>2}{charge:>2}"
            )
            pdb_lines.append(atom_line)

            for prev_atom_idx, prev_atom in atoms_appended_for_res:
                if are_atoms_bonded(res_name_3, atom_name, prev_atom):
                    conect_line = f"CONECT{prev_atom_idx:5d}{atom_index:5d}\n"
                    conect_lines.append(conect_line)
            atoms_appended_for_res.append((atom_index, atom_name))
            if atom_name == "N":
                n_atom_idx = atom_index
            if atom_name == "C":
                c_atom_idx = atom_index

            atom_index += 1

        if i > 0:
            conect_line = f"CONECT{prev_c_atom_idx:5d}{n_atom_idx:5d}\n"
            conect_lines.append(conect_line)
        prev_c_atom_idx = c_atom_idx

    # Close the final chain.
    pdb_lines.append(
        _chain_end(
            atom_index,
            res_1to3(aatype[-1]),
            chain_ids[chain_index[-1]],
            residue_index[-1],
        )
    )
    pdb_lines.append("ENDMDL")
    pdb_lines.append("END")

    # Pad all lines to 80 characters.
    pdb_lines = [line.ljust(80) for line in pdb_lines]
    pdb_str = "\n".join(pdb_lines) + "\n"  # Add terminating newline.
    if conect:
        conect_str = "".join(conect_lines) + "\n"
        return pdb_str, conect_str
    return pdb_str


def ideal_atom_mask(prot: Protein) -> np.ndarray:
    """Computes an ideal atom mask.

    `Protein.atom_mask` typically is defined according to the atoms that are
    reported in the PDB. This function computes a mask according to heavy atoms
    that should be present in the given sequence of amino acids.

    Args:
      prot: `Protein` whose fields are `numpy.ndarray` objects.

    Returns:
      An ideal atom mask.
    """
    return residue_constants.STANDARD_ATOM_MASK[prot.aatype]


def from_prediction(
    features: FeatureDict,
    result: ModelOutput,
    b_factors: Optional[np.ndarray] = None,
    remove_leading_feature_dimension: bool = True,
) -> Protein:
    """Assembles a protein from a prediction.

    Args:
      features: Dictionary holding model inputs.
      result: Dictionary holding model outputs.
      b_factors: (Optional) B-factors to use for the protein.
      remove_leading_feature_dimension: Whether to remove the leading dimension
        of the `features` values.

    Returns:
      A protein instance.
    """
    fold_output = result["structure_module"]

    def _maybe_remove_leading_dim(arr: np.ndarray) -> np.ndarray:
        return arr[0] if remove_leading_feature_dimension else arr

    if "asym_id" in features:
        chain_index = _maybe_remove_leading_dim(features["asym_id"])
    else:
        chain_index = np.zeros_like(_maybe_remove_leading_dim(features["aatype"]))

    if b_factors is None:
        b_factors = np.zeros_like(fold_output["final_atom_mask"])

    return Protein(
        aatype=_maybe_remove_leading_dim(features["aatype"]),
        atom_positions=fold_output["final_atom_positions"],
        atom_mask=fold_output["final_atom_mask"],
        residue_index=_maybe_remove_leading_dim(features["residue_index"]) + 1,
        chain_index=chain_index,
        b_factors=b_factors,
    )