from pathlib import Path import sys _PROJECT_FILE = Path(__file__).resolve() for _PROJECT_ROOT in _PROJECT_FILE.parents: if (_PROJECT_ROOT / "model").is_dir(): if str(_PROJECT_ROOT) not in sys.path: sys.path.insert(0, str(_PROJECT_ROOT)) break # Copyright (c) Meta Platforms, Inc. and affiliates. # # This source code is licensed under the MIT license found in the # LICENSE file in the root directory of this source tree. # # Scores sequences based on a given structure. # # usage: # score_log_likelihoods.py [-h] [--outpath OUTPATH] [--chain CHAIN] pdbfile seqfile import argparse from biotite.sequence.io.fasta import FastaFile, get_sequences import numpy as np from pathlib import Path import torch import torch.nn.functional as F from tqdm import tqdm import model.esm as esm import model.esm.inverse_folding def score_singlechain_backbone(model, alphabet, args): if torch.cuda.is_available() and not args.nogpu: model = model.cuda() print("Transferred model to GPU") coords, native_seq = esm.inverse_folding.util.load_coords(args.pdbfile, args.chain) print('Native sequence loaded from structure file:') print(native_seq) print('\n') ll, _ = esm.inverse_folding.util.score_sequence( model, alphabet, coords, native_seq) print('Native sequence') print(f'Log likelihood: {ll:.2f}') print(f'Perplexity: {np.exp(-ll):.2f}') print('\nScoring variant sequences from sequence file..\n') infile = FastaFile() infile.read(args.seqfile) seqs = get_sequences(infile) Path(args.outpath).parent.mkdir(parents=True, exist_ok=True) with open(args.outpath, 'w') as fout: fout.write('seqid,log_likelihood\n') for header, seq in tqdm(seqs.items()): ll, _ = esm.inverse_folding.util.score_sequence( model, alphabet, coords, str(seq)) fout.write(header + ',' + str(ll) + '\n') print(f'Results saved to {args.outpath}') def score_multichain_backbone(model, alphabet, args): if torch.cuda.is_available() and not args.nogpu: model = model.cuda() print("Transferred model to GPU") structure = esm.inverse_folding.util.load_structure(args.pdbfile) coords, native_seqs = esm.inverse_folding.multichain_util.extract_coords_from_complex(structure) target_chain_id = args.chain native_seq = native_seqs[target_chain_id] print('Native sequence loaded from structure file:') print(native_seq) print('\n') ll, _ = esm.inverse_folding.multichain_util.score_sequence_in_complex( model, alphabet, coords, target_chain_id, native_seq) print('Native sequence') print(f'Log likelihood: {ll:.2f}') print(f'Perplexity: {np.exp(-ll):.2f}') print('\nScoring variant sequences from sequence file..\n') infile = FastaFile() infile.read(args.seqfile) seqs = get_sequences(infile) Path(args.outpath).parent.mkdir(parents=True, exist_ok=True) with open(args.outpath, 'w') as fout: fout.write('seqid,log_likelihood\n') for header, seq in tqdm(seqs.items()): ll, _ = esm.inverse_folding.multichain_util.score_sequence_in_complex( model, alphabet, coords, target_chain_id, str(seq)) fout.write(header + ',' + str(ll) + '\n') print(f'Results saved to {args.outpath}') def main(): parser = argparse.ArgumentParser( description='Score sequences based on a given structure.' ) parser.add_argument( 'pdbfile', type=str, help='input filepath, either .pdb or .cif', ) parser.add_argument( 'seqfile', type=str, help='input filepath for variant sequences in a .fasta file', ) parser.add_argument( '--outpath', type=str, help='output filepath for scores of variant sequences', default='output/sequence_scores.csv', ) parser.add_argument( '--chain', type=str, help='chain id for the chain of interest', default='A', ) parser.set_defaults(multichain_backbone=False) parser.add_argument( '--multichain-backbone', action='store_true', help='use the backbones of all chains in the input for conditioning' ) parser.add_argument( '--singlechain-backbone', dest='multichain_backbone', action='store_false', help='use the backbone of only target chain in the input for conditioning' ) parser.add_argument("--nogpu", action="store_true", help="Do not use GPU even if available") args = parser.parse_args() model, alphabet = esm.pretrained.esm_if1_gvp4_t16_142M_UR50() model = model.eval() if args.multichain_backbone: score_multichain_backbone(model, alphabet, args) else: score_singlechain_backbone(model, alphabet, args) if __name__ == '__main__': main()