Datasets:

jglaser
/

pdb_protein_ligand_complexes

Tags:

use openfold features

28974f4 about 4 years ago

12.5 kB

#!/usr/bin/env python

# Split a protein-ligand complex into protein and ligands and assign ligand bond orders using SMILES strings from Ligand Export
# Code requires Python 3.6

import sys
from prody import *
import pandas as pd
from rdkit import Chem
from rdkit.Chem import AllChem
from io import StringIO
import requests

from mpi4py import MPI
from mpi4py.futures import MPICommExecutor
from mpi4py.futures import MPIPoolExecutor

import re
from functools import partial
import gzip
from rdkit.Chem.Descriptors import ExactMolWt
import numpy as np

import os
import random
import traceback

from openfold import data_transforms, protein
from openfold.residue_constants import aatype_to_str_sequence
import torch

# minimum molecular weight to consider sth a ligand
mol_wt_cutoff = 100

# minimum number of atoms
min_atoms = 3

# all punctuation
punctuation_regex  = r"""(\(|\)|\.|=|#|-|\+|\\|\/|:|~|@|\?|>>?|\*|\$|\%[0-9]{2}|[0-9])"""

# tokenization regex (Schwaller)
molecule_regex = r"""(\[[^\]]+]|Br?|Cl?|N|O|S|P|F|I|b|c|n|o|s|p|\(|\)|\.|=|#|-|\+|\\|\/|:|~|@|\?|>>?|\*|\$|\%[0-9]{2}|[0-9])"""

# filter out these common additives which occur in more than 75 complexes in the PDB
ubiquitous_ligands = ['PEG', 'ADP', 'FAD', 'NAD', 'ATP', 'MPD', 'NAP', 'GDP', 'MES',
       'GTP', 'FMN', 'HEC', 'TRS', 'CIT', 'PGE', 'ANP', 'SAH', 'NDP',
       'PG4', 'EPE', 'AMP', 'COA', 'MLI', 'FES', 'GNP', 'MRD', 'GSH',
       'FLC', 'AGS', 'NAI', 'SAM', 'PCW', '1PE', 'TLA', 'BOG', 'CYC',
       'UDP', 'PX4', 'NAG', 'IMP', 'POP', 'UMP', 'PLM', 'HEZ', 'TPP',
       'ACP', 'LDA', 'ACO', 'CLR', 'BGC', 'P6G', 'LMT', 'OGA', 'DTT',
       'POV', 'FBP', 'AKG', 'MLA', 'ADN', 'NHE', '7Q9', 'CMP', 'BTB',
       'PLP', 'CAC', 'SIN', 'C2E', '2AN', 'OCT', '17F', 'TAR', 'BTN',
       'XYP', 'MAN', '5GP', 'GAL', 'GLC', 'DTP', 'DGT', 'PEB', 'THP',
       'BEZ', 'CTP', 'GSP', 'HED', 'ADE', 'TYD', 'TTP', 'BNG', 'IHP',
       'FDA', 'PEP', 'ALF', 'APR', 'MTX', 'MLT', 'LU8', 'UTP', 'APC',
       'BLA', 'C8E', 'D10', 'CHT', 'BO2', '3BV', 'ORO', 'MPO', 'Y01',
       'OLC', 'B3P', 'G6P', 'PMP', 'D12', 'NDG', 'A3P', '78M', 'F6P',
       'U5P', 'PRP', 'UPG', 'THM', 'SFG', 'MYR', 'FEO', 'PG0', 'CXS',
       'AR6', 'CHD', 'WO4', 'C5P', 'UFP', 'GCP', 'HDD', 'SRT', 'STU',
       'CDP', 'TCL', '04C', 'MYA', 'URA', 'PLG', 'MTA', 'BMP', 'SAL',
       'TA1', 'UD1', 'OLA', 'BCN', 'LMR', 'BMA', 'OAA', 'TAM', 'MBO',
       'MMA', 'SPD', 'MTE', 'AP5', 'TMP', 'PGA', 'GLA', '3PG', 'FUL',
       'PQQ', '9TY', 'DUR', 'PPV', 'SPM', 'SIA', 'DUP', 'GTX', '1PG',
       'GUN', 'ETF', 'FDP', 'MFU', 'G2P', 'PC', 'DST', 'INI']

def get_protein_sequence_and_coords(receptor, pdb_str):
    chains = [chain.getChid() for chain in receptor.getHierView()]

    aatype = []
    atom_positions = []
    atom_mask = []
    for chain in chains:
        p = protein.from_pdb_string(pdb_str, chain)
        aatype.append(p.aatype)
        atom_positions.append(p.atom_positions)
        atom_mask.append(p.atom_mask)

    # concatenate chains
    aatype = np.concatenate(aatype)
    atom_positions = np.concatenate(atom_positions)
    atom_mask = np.concatenate(atom_mask)

    # determine torsion angles
    features = {'aatype': torch.tensor(aatype),
                'all_atom_positions': torch.tensor(atom_positions),
                'all_atom_mask': torch.tensor(atom_mask)}
    features = data_transforms.atom37_to_torsion_angles()(features)
    features = data_transforms.atom37_to_frames(features)
    features = data_transforms.make_atom14_masks(features)
    features = data_transforms.make_atom14_positions(features)
    features = {k: v.numpy() for k, v in features.items() if isinstance(v, torch.Tensor)}

    seq = aatype_to_str_sequence(aatype)

    return seq, features

def tokenize_ligand(mol):
    # convert to SMILES and map atoms
    smi = Chem.MolToSmiles(mol)

    # position of atoms in SMILES (not counting punctuation)
    atom_order = [int(s) for s in list(filter(None,re.sub(r'[\[\]]','',mol.GetProp("_smilesAtomOutputOrder")).split(',')))]

    # tokenize the SMILES
    tokens = list(filter(None, re.split(molecule_regex, smi)))

    # remove punctuation
    masked_tokens = [re.sub(punctuation_regex,'',s) for s in tokens]

    k = 0
    token_pos = []
    for i,token in enumerate(masked_tokens):
        if token != '':
            token_pos.append(tuple(mol.GetConformer().GetAtomPosition(atom_order[k])))
            k += 1
        else:
            token_pos.append((np.nan, np.nan, np.nan))

    k = 0
    conf_2d = AllChem.Compute2DCoords(mol)
    token_pos_2d = []
    atom_idx = []
    for i,token in enumerate(masked_tokens):
        if token != '':
            token_pos_2d.append(tuple(mol.GetConformer(conf_2d).GetAtomPosition(atom_order[k])))
            atom_idx.append(atom_order[k])
            k += 1
        else:
            token_pos_2d.append((0.,0.,0.))
            atom_idx.append(None)

    return smi, token_pos, token_pos_2d, atom_idx

def read_ligand_expo():
    """
    Read Ligand Expo data, try to find a file called
    Components-smiles-stereo-oe.smi in the current directory.
    If you can't find the file, grab it from the RCSB
    :return: Ligand Expo as a dictionary with ligand id as the key
    """
    file_name = "Components-smiles-stereo-oe.smi"
    try:
        df = pd.read_csv(file_name, sep=r"[\t]+",
                         header=None,
                         names=["SMILES", "ID", "Name"],
                         engine='python')
    except FileNotFoundError:
        url = f"http://ligand-expo.rcsb.org/dictionaries/{file_name}"
        print(url)
        r = requests.get(url, allow_redirects=True)
        open('Components-smiles-stereo-oe.smi', 'wb').write(r.content)
        df = pd.read_csv(file_name, sep="\t",
                         header=None,
                         names=["SMILES", "ID", "Name"],
                         na_filter=False)
    return df


def get_pdb_components(pdb_id):
    """
    Split a protein-ligand pdb into protein and ligand components
    :param pdb_id:
    :return:
    """
    with gzip.open(pdb_id,'rt') as f:
        pdb = parsePDBStream(f)

    protein = pdb.select('protein')
    ligand = pdb.select('not protein and not water')
    return protein, ligand


def process_ligand(ligand, res_name, df_expo):
    """
    Add bond orders to a pdb ligand
    1. Select the ligand component with name "res_name"
    2. Get the corresponding SMILES from the Ligand Expo dictionary
    3. Create a template molecule from the SMILES in step 2
    4. Write the PDB file to a stream
    5. Read the stream into an RDKit molecule
    6. Assign the bond orders from the template from step 3
    :param ligand: ligand as generated by prody
    :param res_name: residue name of ligand to extract
    :param df_expo: dictionary with LigandExpo
    :return: molecule with bond orders assigned
    """
    sub_smiles = df_expo[df_expo['ID'].values == res_name]['SMILES'].values[0]
    template = AllChem.MolFromSmiles(sub_smiles)

    allres = ligand.select(f"resname {res_name}")
    res = np.unique(allres.getResindices())
    mols = []
    for i in res:
        sub_mol = ligand.select(f"resname {res_name} and resindex {i}")
        output = StringIO()
        writePDBStream(output, sub_mol)
        pdb_string = output.getvalue()
        rd_mol = AllChem.MolFromPDBBlock(pdb_string)
        mols.append(AllChem.AssignBondOrdersFromTemplate(template, rd_mol))
    return mols, template

def rot_from_two_vecs(e0_unnormalized, e1_unnormalized):
    """Create rotation matrices from unnormalized vectors for the x and y-axes.
    This creates a rotation matrix from two vectors using Gram-Schmidt
    orthogonalization.
    Args:
    e0_unnormalized: vectors lying along x-axis of resulting rotation
    e1_unnormalized: vectors lying in xy-plane of resulting rotation
    Returns:
    Rotations resulting from Gram-Schmidt procedure.
    """
    # Normalize the unit vector for the x-axis, e0.
    e0 = e0_unnormalized / np.linalg.norm(e0_unnormalized)

    # make e1 perpendicular to e0.
    c = np.dot(e1_unnormalized, e0)
    e1 = e1_unnormalized - c * e0
    e1 = e1 / np.linalg.norm(e1)

    # Compute e2 as cross product of e0 and e1.
    e2 = np.cross(e0, e1)

    # local to space frame
    return np.stack([e0,e1,e2]).T

def process_entry(df, pdb_fn):
    try:
        """
        Slit pdb into protein and ligands,
        parse protein sequence and ligand tokens
        :param df: ligand expo data
        :param pdb_fn: pdb entry file name
        :return:
        """
        protein, ligand = get_pdb_components(pdb_fn)

        pdb_name = os.path.basename(pdb_fn).split('.')[-3][3:]

        ligand_mols = []
        ligand_names = []
        ligand_bonds = []
        if ligand is not None:
            # filter ligands by molecular weight
            res_name_list = list(set(ligand.getResnames()))
            for res in res_name_list:
                if res in ubiquitous_ligands:
                    continue
                mols, template = process_ligand(ligand, res, df)

                mol_wt = ExactMolWt(template)
                natoms = template.GetNumAtoms()

                if mol_wt >= mol_wt_cutoff and natoms >= min_atoms:
                    # only use first copy of ligand
                    mols = mols[:1]
                    ligand_mols += mols
                    ligand_names += [res]*len(mols)

                    bonds = []
                    for b in template.GetBonds():
                        bonds.append((b.GetBeginAtomIdx(), b.GetEndAtomIdx()))
                    ligand_bonds.append(bonds)


        ligand_smiles = []
        ligand_xyz = []
        ligand_xyz_2d = []
        ligand_token_bonds = []
        for mol, name, bonds in zip(ligand_mols, ligand_names, ligand_bonds):
            print('Processing {} and {}'.format(pdb_name, name))
            smi, xyz, xyz_2d, atom_idx = tokenize_ligand(mol)
            ligand_smiles.append(smi)
            ligand_xyz.append(xyz)
            ligand_xyz_2d.append(xyz_2d)

            ligand_token_bonds.append([ (atom_idx.index(b[0]), atom_idx.index(b[1])) for b in bonds ])

        pdb_str = StringIO()
        writePDBStream(pdb_str, protein)

        seq, features = get_protein_sequence_and_coords(protein, pdb_str.getvalue())
        features = { 'rigidgroups_gt_frames': features['rigidgroups_gt_frames'],
                    'torsion_angles_sin_cos': features['torsion_angles_sin_cos']}
        return pdb_name, seq, features, ligand_names, ligand_smiles, ligand_xyz, ligand_xyz_2d, ligand_token_bonds
    except Exception as e:
        print(traceback.format_exc())
        print(repr(e))

def write_result(fn, data):
    # expand sequences and ligands
    pdb_id = [r[0] for r in data if r is not None for ligand in r[3]]
    seq = [r[1] for r in data if r is not None for ligand in r[3]]
    receptor_features = [r[2] for r in data if r is not None for ligand in r[3]]
    lig_id = [l for r in data if r is not None for l in r[3]]
    lig_smiles = [s for r in data if r is not None for s in r[4]]
    lig_xyz = [xyz for r in data if r is not None for xyz in r[5]]
    lig_xyz_2d = [xyz for r in data if r is not None for xyz in r[6]]
    lig_bonds = [b for r in data if r is not None for b in r[7]]

    import pandas as pd
    df = pd.DataFrame({
        'pdb_id': pdb_id,
        'lig_id': lig_id,
        'seq': seq,
        'smiles': lig_smiles,
        'receptor_features': receptor_features,
        'ligand_xyz': lig_xyz,
        'ligand_xyz_2d': lig_xyz_2d,
        'ligand_bonds': lig_bonds})
    df.to_pickle(fn)

if __name__ == '__main__':
    import glob

    filenames = glob.glob('pdb/*/*.gz')
    filenames = sorted(filenames)

    random.seed(42)
    random.shuffle(filenames)

    split_idx = int(0.9*len(filenames))
    train = filenames[:split_idx]
    test = filenames[split_idx:]

    comm = MPI.COMM_WORLD
    with MPICommExecutor(comm, root=0) as executor:
#    with MPIPoolExecutor() as executor:
        if executor is not None:
            # read ligand table
            df = read_ligand_expo()

            result = executor.map(partial(process_entry, df), train, chunksize=128)
            result = list(result)

            write_result('data/pdb_train.p', result)

            result = executor.map(partial(process_entry, df), test, chunksize=128)
            result = list(result)

            write_result('data/pdb_test.p', result)

	#!/usr/bin/env python

	# Split a protein-ligand complex into protein and ligands and assign ligand bond orders using SMILES strings from Ligand Export
	# Code requires Python 3.6

	import sys
	from prody import *
	import pandas as pd
	from rdkit import Chem
	from rdkit.Chem import AllChem
	from io import StringIO
	import requests

	from mpi4py import MPI
	from mpi4py.futures import MPICommExecutor
	from mpi4py.futures import MPIPoolExecutor

	import re
	from functools import partial
	import gzip
	from rdkit.Chem.Descriptors import ExactMolWt
	import numpy as np

	import os
	import random
	import traceback

	from openfold import data_transforms, protein
	from openfold.residue_constants import aatype_to_str_sequence
	import torch

	# minimum molecular weight to consider sth a ligand
	mol_wt_cutoff = 100

	# minimum number of atoms
	min_atoms = 3

	# all punctuation
	punctuation_regex = r"""(\(\|\)\|\.\|=\|#\|-\|\+\|\\\|\/\|:\|~\|@\|\?\|>>?\|\*\|\$\|\%[0-9]{2}\|[0-9])"""

	# tokenization regex (Schwaller)
	molecule_regex = r"""(\[[^\]]+]\|Br?\|Cl?\|N\|O\|S\|P\|F\|I\|b\|c\|n\|o\|s\|p\|\(\|\)\|\.\|=\|#\|-\|\+\|\\\|\/\|:\|~\|@\|\?\|>>?\|\*\|\$\|\%[0-9]{2}\|[0-9])"""

	# filter out these common additives which occur in more than 75 complexes in the PDB
	ubiquitous_ligands = ['PEG', 'ADP', 'FAD', 'NAD', 'ATP', 'MPD', 'NAP', 'GDP', 'MES',
	'GTP', 'FMN', 'HEC', 'TRS', 'CIT', 'PGE', 'ANP', 'SAH', 'NDP',
	'PG4', 'EPE', 'AMP', 'COA', 'MLI', 'FES', 'GNP', 'MRD', 'GSH',
	'FLC', 'AGS', 'NAI', 'SAM', 'PCW', '1PE', 'TLA', 'BOG', 'CYC',
	'UDP', 'PX4', 'NAG', 'IMP', 'POP', 'UMP', 'PLM', 'HEZ', 'TPP',
	'ACP', 'LDA', 'ACO', 'CLR', 'BGC', 'P6G', 'LMT', 'OGA', 'DTT',
	'POV', 'FBP', 'AKG', 'MLA', 'ADN', 'NHE', '7Q9', 'CMP', 'BTB',
	'PLP', 'CAC', 'SIN', 'C2E', '2AN', 'OCT', '17F', 'TAR', 'BTN',
	'XYP', 'MAN', '5GP', 'GAL', 'GLC', 'DTP', 'DGT', 'PEB', 'THP',
	'BEZ', 'CTP', 'GSP', 'HED', 'ADE', 'TYD', 'TTP', 'BNG', 'IHP',
	'FDA', 'PEP', 'ALF', 'APR', 'MTX', 'MLT', 'LU8', 'UTP', 'APC',
	'BLA', 'C8E', 'D10', 'CHT', 'BO2', '3BV', 'ORO', 'MPO', 'Y01',
	'OLC', 'B3P', 'G6P', 'PMP', 'D12', 'NDG', 'A3P', '78M', 'F6P',
	'U5P', 'PRP', 'UPG', 'THM', 'SFG', 'MYR', 'FEO', 'PG0', 'CXS',
	'AR6', 'CHD', 'WO4', 'C5P', 'UFP', 'GCP', 'HDD', 'SRT', 'STU',
	'CDP', 'TCL', '04C', 'MYA', 'URA', 'PLG', 'MTA', 'BMP', 'SAL',
	'TA1', 'UD1', 'OLA', 'BCN', 'LMR', 'BMA', 'OAA', 'TAM', 'MBO',
	'MMA', 'SPD', 'MTE', 'AP5', 'TMP', 'PGA', 'GLA', '3PG', 'FUL',
	'PQQ', '9TY', 'DUR', 'PPV', 'SPM', 'SIA', 'DUP', 'GTX', '1PG',
	'GUN', 'ETF', 'FDP', 'MFU', 'G2P', 'PC', 'DST', 'INI']

	def get_protein_sequence_and_coords(receptor, pdb_str):
	chains = [chain.getChid() for chain in receptor.getHierView()]

	aatype = []
	atom_positions = []
	atom_mask = []
	for chain in chains:
	p = protein.from_pdb_string(pdb_str, chain)
	aatype.append(p.aatype)
	atom_positions.append(p.atom_positions)
	atom_mask.append(p.atom_mask)

	# concatenate chains
	aatype = np.concatenate(aatype)
	atom_positions = np.concatenate(atom_positions)
	atom_mask = np.concatenate(atom_mask)

	# determine torsion angles
	features = {'aatype': torch.tensor(aatype),
	'all_atom_positions': torch.tensor(atom_positions),
	'all_atom_mask': torch.tensor(atom_mask)}
	features = data_transforms.atom37_to_torsion_angles()(features)
	features = data_transforms.atom37_to_frames(features)
	features = data_transforms.make_atom14_masks(features)
	features = data_transforms.make_atom14_positions(features)
	features = {k: v.numpy() for k, v in features.items() if isinstance(v, torch.Tensor)}

	seq = aatype_to_str_sequence(aatype)

	return seq, features

	def tokenize_ligand(mol):
	# convert to SMILES and map atoms
	smi = Chem.MolToSmiles(mol)

	# position of atoms in SMILES (not counting punctuation)
	atom_order = [int(s) for s in list(filter(None,re.sub(r'[\[\]]','',mol.GetProp("_smilesAtomOutputOrder")).split(',')))]

	# tokenize the SMILES
	tokens = list(filter(None, re.split(molecule_regex, smi)))

	# remove punctuation
	masked_tokens = [re.sub(punctuation_regex,'',s) for s in tokens]

	k = 0
	token_pos = []
	for i,token in enumerate(masked_tokens):
	if token != '':
	token_pos.append(tuple(mol.GetConformer().GetAtomPosition(atom_order[k])))
	k += 1
	else:
	token_pos.append((np.nan, np.nan, np.nan))

	k = 0
	conf_2d = AllChem.Compute2DCoords(mol)
	token_pos_2d = []
	atom_idx = []
	for i,token in enumerate(masked_tokens):
	if token != '':
	token_pos_2d.append(tuple(mol.GetConformer(conf_2d).GetAtomPosition(atom_order[k])))
	atom_idx.append(atom_order[k])
	k += 1
	else:
	token_pos_2d.append((0.,0.,0.))
	atom_idx.append(None)

	return smi, token_pos, token_pos_2d, atom_idx

	def read_ligand_expo():
	"""
	Read Ligand Expo data, try to find a file called
	Components-smiles-stereo-oe.smi in the current directory.
	If you can't find the file, grab it from the RCSB
	:return: Ligand Expo as a dictionary with ligand id as the key
	"""
	file_name = "Components-smiles-stereo-oe.smi"
	try:
	df = pd.read_csv(file_name, sep=r"[\t]+",
	header=None,
	names=["SMILES", "ID", "Name"],
	engine='python')
	except FileNotFoundError:
	url = f"http://ligand-expo.rcsb.org/dictionaries/{file_name}"
	print(url)
	r = requests.get(url, allow_redirects=True)
	open('Components-smiles-stereo-oe.smi', 'wb').write(r.content)
	df = pd.read_csv(file_name, sep="\t",
	header=None,
	names=["SMILES", "ID", "Name"],
	na_filter=False)
	return df


	def get_pdb_components(pdb_id):
	"""
	Split a protein-ligand pdb into protein and ligand components
	:param pdb_id:
	:return:
	"""
	with gzip.open(pdb_id,'rt') as f:
	pdb = parsePDBStream(f)

	protein = pdb.select('protein')
	ligand = pdb.select('not protein and not water')
	return protein, ligand


	def process_ligand(ligand, res_name, df_expo):
	"""
	Add bond orders to a pdb ligand
	1. Select the ligand component with name "res_name"
	2. Get the corresponding SMILES from the Ligand Expo dictionary
	3. Create a template molecule from the SMILES in step 2
	4. Write the PDB file to a stream
	5. Read the stream into an RDKit molecule
	6. Assign the bond orders from the template from step 3
	:param ligand: ligand as generated by prody
	:param res_name: residue name of ligand to extract
	:param df_expo: dictionary with LigandExpo
	:return: molecule with bond orders assigned
	"""
	sub_smiles = df_expo[df_expo['ID'].values == res_name]['SMILES'].values[0]
	template = AllChem.MolFromSmiles(sub_smiles)

	allres = ligand.select(f"resname {res_name}")
	res = np.unique(allres.getResindices())
	mols = []
	for i in res:
	sub_mol = ligand.select(f"resname {res_name} and resindex {i}")
	output = StringIO()
	writePDBStream(output, sub_mol)
	pdb_string = output.getvalue()
	rd_mol = AllChem.MolFromPDBBlock(pdb_string)
	mols.append(AllChem.AssignBondOrdersFromTemplate(template, rd_mol))
	return mols, template

	def rot_from_two_vecs(e0_unnormalized, e1_unnormalized):
	"""Create rotation matrices from unnormalized vectors for the x and y-axes.
	This creates a rotation matrix from two vectors using Gram-Schmidt
	orthogonalization.
	Args:
	e0_unnormalized: vectors lying along x-axis of resulting rotation
	e1_unnormalized: vectors lying in xy-plane of resulting rotation
	Returns:
	Rotations resulting from Gram-Schmidt procedure.
	"""
	# Normalize the unit vector for the x-axis, e0.
	e0 = e0_unnormalized / np.linalg.norm(e0_unnormalized)

	# make e1 perpendicular to e0.
	c = np.dot(e1_unnormalized, e0)
	e1 = e1_unnormalized - c * e0
	e1 = e1 / np.linalg.norm(e1)

	# Compute e2 as cross product of e0 and e1.
	e2 = np.cross(e0, e1)

	# local to space frame
	return np.stack([e0,e1,e2]).T

	def process_entry(df, pdb_fn):
	try:
	"""
	Slit pdb into protein and ligands,
	parse protein sequence and ligand tokens
	:param df: ligand expo data
	:param pdb_fn: pdb entry file name
	:return:
	"""
	protein, ligand = get_pdb_components(pdb_fn)

	pdb_name = os.path.basename(pdb_fn).split('.')[-3][3:]

	ligand_mols = []
	ligand_names = []
	ligand_bonds = []
	if ligand is not None:
	# filter ligands by molecular weight
	res_name_list = list(set(ligand.getResnames()))
	for res in res_name_list:
	if res in ubiquitous_ligands:
	continue
	mols, template = process_ligand(ligand, res, df)

	mol_wt = ExactMolWt(template)
	natoms = template.GetNumAtoms()

	if mol_wt >= mol_wt_cutoff and natoms >= min_atoms:
	# only use first copy of ligand
	mols = mols[:1]
	ligand_mols += mols
	ligand_names += [res]*len(mols)

	bonds = []
	for b in template.GetBonds():
	bonds.append((b.GetBeginAtomIdx(), b.GetEndAtomIdx()))
	ligand_bonds.append(bonds)


	ligand_smiles = []
	ligand_xyz = []
	ligand_xyz_2d = []
	ligand_token_bonds = []
	for mol, name, bonds in zip(ligand_mols, ligand_names, ligand_bonds):
	print('Processing {} and {}'.format(pdb_name, name))
	smi, xyz, xyz_2d, atom_idx = tokenize_ligand(mol)
	ligand_smiles.append(smi)
	ligand_xyz.append(xyz)
	ligand_xyz_2d.append(xyz_2d)

	ligand_token_bonds.append([ (atom_idx.index(b[0]), atom_idx.index(b[1])) for b in bonds ])

	pdb_str = StringIO()
	writePDBStream(pdb_str, protein)

	seq, features = get_protein_sequence_and_coords(protein, pdb_str.getvalue())
	features = { 'rigidgroups_gt_frames': features['rigidgroups_gt_frames'],
	'torsion_angles_sin_cos': features['torsion_angles_sin_cos']}
	return pdb_name, seq, features, ligand_names, ligand_smiles, ligand_xyz, ligand_xyz_2d, ligand_token_bonds
	except Exception as e:
	print(traceback.format_exc())
	print(repr(e))

	def write_result(fn, data):
	# expand sequences and ligands
	pdb_id = [r[0] for r in data if r is not None for ligand in r[3]]
	seq = [r[1] for r in data if r is not None for ligand in r[3]]
	receptor_features = [r[2] for r in data if r is not None for ligand in r[3]]
	lig_id = [l for r in data if r is not None for l in r[3]]
	lig_smiles = [s for r in data if r is not None for s in r[4]]
	lig_xyz = [xyz for r in data if r is not None for xyz in r[5]]
	lig_xyz_2d = [xyz for r in data if r is not None for xyz in r[6]]
	lig_bonds = [b for r in data if r is not None for b in r[7]]

	import pandas as pd
	df = pd.DataFrame({
	'pdb_id': pdb_id,
	'lig_id': lig_id,
	'seq': seq,
	'smiles': lig_smiles,
	'receptor_features': receptor_features,
	'ligand_xyz': lig_xyz,
	'ligand_xyz_2d': lig_xyz_2d,
	'ligand_bonds': lig_bonds})
	df.to_pickle(fn)

	if __name__ == '__main__':
	import glob

	filenames = glob.glob('pdb//.gz')
	filenames = sorted(filenames)

	random.seed(42)
	random.shuffle(filenames)

	split_idx = int(0.9*len(filenames))
	train = filenames[:split_idx]
	test = filenames[split_idx:]

	comm = MPI.COMM_WORLD
	with MPICommExecutor(comm, root=0) as executor:
	# with MPIPoolExecutor() as executor:
	if executor is not None:
	# read ligand table
	df = read_ligand_expo()

	result = executor.map(partial(process_entry, df), train, chunksize=128)
	result = list(result)

	write_result('data/pdb_train.p', result)

	result = executor.map(partial(process_entry, df), test, chunksize=128)
	result = list(result)

	write_result('data/pdb_test.p', result)