mirror of
https://github.com/baker-laboratory/RoseTTAFold-All-Atom.git
synced 2024-11-14 22:33:58 +00:00
812 lines
27 KiB
Python
812 lines
27 KiB
Python
import numpy as np
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import scipy
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import scipy.spatial
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import string
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import os,re
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from os.path import exists
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import random
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import rf2aa.util as util
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import gzip
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import rf2aa
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from rf2aa.ffindex import *
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import torch
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from openbabel import openbabel
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from rf2aa.chemical import ChemicalData as ChemData
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def get_dislf(seq, xyz, mask):
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L = seq.shape[0]
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resolved_cys_mask = ((seq==ChemData().aa2num['CYS']) * mask[:,5]).nonzero().squeeze(-1) # cys[5]=='sg'
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sgs = xyz[resolved_cys_mask,5]
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ii,jj = torch.triu_indices(sgs.shape[0],sgs.shape[0],1)
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d_sg_sg = torch.linalg.norm(sgs[ii,:]-sgs[jj,:], dim=-1)
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is_dslf = (d_sg_sg>1.7)*(d_sg_sg<2.3)
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dslf = []
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for i in is_dslf.nonzero():
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dslf.append( (
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resolved_cys_mask[ii[i]].item(),
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resolved_cys_mask[jj[i]].item(),
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) )
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return dslf
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def read_template_pdb(L, pdb_fn, target_chain=None):
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# get full sequence from given PDB
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seq_full = list()
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prev_chain=''
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with open(pdb_fn) as fp:
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for line in fp:
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if line[:4] != "ATOM":
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continue
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if line[12:16].strip() != "CA":
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continue
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if line[21] != prev_chain:
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if len(seq_full) > 0:
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L_s.append(len(seq_full)-offset)
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offset = len(seq_full)
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prev_chain = line[21]
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aa = line[17:20]
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seq_full.append(ChemData().aa2num[aa] if aa in ChemData().aa2num.keys() else 20)
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seq_full = torch.tensor(seq_full).long()
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xyz = torch.full((L, 36, 3), np.nan).float()
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seq = torch.full((L,), 20).long()
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conf = torch.zeros(L,1).float()
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with open(pdb_fn) as fp:
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for line in fp:
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if line[:4] != "ATOM":
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continue
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resNo, atom, aa = int(line[22:26]), line[12:16], line[17:20]
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aa_idx = ChemData().aa2num[aa] if aa in ChemData().aa2num.keys() else 20
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#
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idx = resNo - 1
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for i_atm, tgtatm in enumerate(ChemData().aa2long[aa_idx]):
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if tgtatm == atom:
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xyz[idx, i_atm, :] = torch.tensor([float(line[30:38]), float(line[38:46]), float(line[46:54])])
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break
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seq[idx] = aa_idx
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mask = torch.logical_not(torch.isnan(xyz[:,:3,0])) # (L, 3)
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mask = mask.all(dim=-1)[:,None]
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conf = torch.where(mask, torch.full((L,1),0.1), torch.zeros(L,1)).float()
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seq_1hot = torch.nn.functional.one_hot(seq, num_classes=32).float()
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t1d = torch.cat((seq_1hot, conf), -1)
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#return seq_full[None], ins[None], L_s, xyz[None], t1d[None]
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return xyz[None], t1d[None]
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def read_multichain_pdb(pdb_fn, tmpl_chain=None, tmpl_conf=0.1):
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print ('read_multichain_pdb',tmpl_chain)
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# get full sequence from PDB
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seq_full = list()
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L_s = list()
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prev_chain=''
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offset = 0
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with open(pdb_fn) as fp:
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for line in fp:
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if line[:4] != "ATOM":
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continue
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if line[12:16].strip() != "CA":
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continue
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if line[21] != prev_chain:
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if len(seq_full) > 0:
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L_s.append(len(seq_full)-offset)
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offset = len(seq_full)
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prev_chain = line[21]
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aa = line[17:20]
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seq_full.append(ChemData().aa2num[aa] if aa in ChemData().aa2num.keys() else 20)
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L_s.append(len(seq_full) - offset)
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seq_full = torch.tensor(seq_full).long()
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L = len(seq_full)
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msa = torch.stack((seq_full,seq_full,seq_full), dim=0)
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msa[1,:L_s[0]] = 20
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msa[2,L_s[0]:] = 20
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ins = torch.zeros_like(msa)
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xyz = ChemData().INIT_CRDS.reshape(1,1,ChemData().NTOTAL,3).repeat(1,L,1,1) + torch.rand(1,L,1,3)*5.0
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xyz_t = ChemData().INIT_CRDS.reshape(1,1,ChemData().NTOTAL,3).repeat(1,L,1,1) + torch.rand(1,L,1,3)*5.0
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mask = torch.full((1, L, ChemData().NTOTAL), False)
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mask_t = torch.full((1, L, ChemData().NTOTAL), False)
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seq = torch.full((1, L,), 20).long()
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conf = torch.zeros(1, L,1).float()
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with open(pdb_fn) as fp:
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for line in fp:
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if line[:4] != "ATOM":
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continue
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outbatch = 0
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resNo, atom, aa = int(line[22:26]), line[12:16], line[17:20]
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aa_idx = ChemData().aa2num[aa] if aa in ChemData().aa2num.keys() else 20
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idx = resNo - 1
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for i_atm, tgtatm in enumerate(ChemData().aa2long[aa_idx]):
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if tgtatm == atom:
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xyz_i = torch.tensor([float(line[30:38]), float(line[38:46]), float(line[46:54])])
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xyz[0, idx, i_atm, :] = xyz_i
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mask[0, idx, i_atm] = True
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if line[21] == tmpl_chain:
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xyz_t[0, idx, i_atm, :] = xyz_i
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mask_t[0, idx, i_atm] = True
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break
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seq[0, idx] = aa_idx
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if (mask_t.any()):
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xyz_t[0] = rf2aa.util.center_and_realign_missing(xyz[0], mask[0])
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dslf = get_dislf(seq[0], xyz[0], mask[0])
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# assign confidence 'CONF' to all residues with backbone in template
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conf = torch.where(mask_t[...,:3].all(dim=-1)[...,None], torch.full((1,L,1),tmpl_conf), torch.zeros(L,1)).float()
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seq_1hot = torch.nn.functional.one_hot(seq, num_classes=ChemData().NAATOKENS-1).float()
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t1d = torch.cat((seq_1hot, conf), -1)
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return msa, ins, L_s, xyz_t, mask_t, t1d, dslf
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def parse_fasta(filename, maxseq=10000, rmsa_alphabet=False):
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msa = []
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ins = []
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fstream = open(filename,"r")
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for line in fstream:
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# skip labels
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if line[0] == '>':
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continue
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# remove right whitespaces
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line = line.rstrip()
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if len(line) == 0:
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continue
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# remove lowercase letters and append to MSA
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msa.append(line)
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# sequence length
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L = len(msa[-1])
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i = np.zeros((L))
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ins.append(i)
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# convert letters into numbers
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if rmsa_alphabet:
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alphabet = np.array(list("00000000000000000000-000000ACGTN"), dtype='|S1').view(np.uint8)
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else:
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alphabet = np.array(list("ARNDCQEGHILKMFPSTWYV-0acgtxbdhuy"), dtype='|S1').view(np.uint8)
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msa = np.array([list(s) for s in msa], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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msa[msa == alphabet[i]] = i
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ins = np.array(ins, dtype=np.uint8)
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return msa,ins
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# Parse a fasta file containing multiple chains separated by '/'
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def parse_multichain_fasta(filename, maxseq=10000, rna_alphabet=False, dna_alphabet=False):
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msa = []
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ins = []
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fstream = open(filename,"r")
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table = str.maketrans(dict.fromkeys(string.ascii_lowercase))
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L_s = []
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for line in fstream:
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# skip labels
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if line[0] == '>':
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continue
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# remove right whitespaces
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line = line.rstrip()
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if len(line) == 0:
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continue
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# remove lowercase letters and append to MSA
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msa_i = line.translate(table)
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msa_i = msa_i.replace('B','D') # hacky...
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if L_s == []:
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L_s = [len(x) for x in msa_i.split('/')]
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msa_i = msa_i.replace('/','')
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msa.append(msa_i)
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# sequence length
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L = len(msa[-1])
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i = np.zeros((L))
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ins.append(i)
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if (len(msa) >= maxseq):
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break
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# convert letters into numbers
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if rna_alphabet:
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alphabet = np.array(list("00000000000000000000-000000ACGTN"), dtype='|S1').view(np.uint8)
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elif dna_alphabet:
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alphabet = np.array(list("00000000000000000000-0ACGTD00000"), dtype='|S1').view(np.uint8)
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else:
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alphabet = np.array(list("ARNDCQEGHILKMFPSTWYV-Xacgtxbdhuy"), dtype='|S1').view(np.uint8)
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msa = np.array([list(s) for s in msa], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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msa[msa == alphabet[i]] = i
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ins = np.array(ins, dtype=np.uint8)
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return msa,ins,L_s
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#fd - parse protein/RNA coupled fastas
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def parse_mixed_fasta(filename, maxseq=10000):
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msa1,msa2 = [],[]
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fstream = open(filename,"r")
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table = str.maketrans(dict.fromkeys(string.ascii_lowercase))
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unpaired_r, unpaired_p = 0, 0
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for line in fstream:
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# skip labels
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if line[0] == '>':
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continue
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# remove right whitespaces
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line = line.rstrip()
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if len(line) == 0:
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continue
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# remove lowercase letters and append to MSA
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msa_i = line.translate(table)
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msa_i = msa_i.replace('B','D') # hacky...
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msas_i = msa_i.split('/')
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if (len(msas_i)==1):
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msas_i = [msas_i[0][:len(msa1[0])], msas_i[0][len(msa1[0]):]]
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if (len(msa1)==0 or (
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len(msas_i[0])==len(msa1[0]) and len(msas_i[1])==len(msa2[0])
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)):
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# skip if we've already found half of our limit in unpaired protein seqs
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if sum([1 for x in msas_i[1] if x != '-']) == 0:
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unpaired_p += 1
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if unpaired_p > maxseq // 2:
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continue
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# skip if we've already found half of our limit in unpaired rna seqs
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if sum([1 for x in msas_i[0] if x != '-']) == 0:
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unpaired_r += 1
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if unpaired_r > maxseq // 2:
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continue
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msa1.append(msas_i[0])
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msa2.append(msas_i[1])
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else:
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print ("Len error",filename, len(msas_i[0]),len(msa1[0]),len(msas_i[1]),len(msas_i[1]))
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if (len(msa1) >= maxseq):
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break
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# convert letters into numbers
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alphabet = np.array(list("ARNDCQEGHILKMFPSTWYV-Xacgtxbdhuy"), dtype='|S1').view(np.uint8)
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msa1 = np.array([list(s) for s in msa1], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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msa1[msa1 == alphabet[i]] = i
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msa1[msa1>=31] = 21 # anything unknown to 'X'
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alphabet = np.array(list("00000000000000000000-000000ACGTN"), dtype='|S1').view(np.uint8)
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msa2 = np.array([list(s) for s in msa2], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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msa2[msa2 == alphabet[i]] = i
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msa2[msa2>=31] = 30 # anything unknown to 'N'
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msa = np.concatenate((msa1,msa2),axis=-1)
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ins = np.zeros(msa.shape, dtype=np.uint8)
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return msa,ins
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# parse a fasta alignment IF it exists
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# otherwise return single-sequence msa
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def parse_fasta_if_exists(seq, filename, maxseq=10000, rmsa_alphabet=False):
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if (exists(filename)):
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return parse_fasta(filename, maxseq, rmsa_alphabet)
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else:
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alphabet = np.array(list("ARNDCQEGHILKMFPSTWYV-0acgtxbdhuy"), dtype='|S1').view(np.uint8) # -0 are UNK/mask
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seq = np.array([list(seq)], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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seq[seq == alphabet[i]] = i
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return (seq, np.zeros_like(seq))
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#fd - parse protein/RNA coupled fastas
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def parse_mixed_fasta(filename, maxseq=8000):
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msa1,msa2 = [],[]
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fstream = open(filename,"r")
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table = str.maketrans(dict.fromkeys(string.ascii_lowercase))
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unpaired_r, unpaired_p = 0, 0
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for line in fstream:
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# skip labels
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if line[0] == '>':
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continue
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# remove right whitespaces
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line = line.rstrip()
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if len(line) == 0:
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continue
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# remove lowercase letters and append to MSA
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msa_i = line.translate(table)
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msa_i = msa_i.replace('B','D') # hacky...
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msas_i = msa_i.split('/')
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if (len(msas_i)==1):
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msas_i = [msas_i[0][:len(msa1[0])], msas_i[0][len(msa1[0]):]]
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if (len(msa1)==0 or (
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len(msas_i[0])==len(msa1[0]) and len(msas_i[1])==len(msa2[0])
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)):
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# skip if we've already found half of our limit in unpaired protein seqs
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if sum([1 for x in msas_i[1] if x != '-']) == 0:
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unpaired_p += 1
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if unpaired_p > maxseq // 2:
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continue
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# skip if we've already found half of our limit in unpaired rna seqs
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if sum([1 for x in msas_i[0] if x != '-']) == 0:
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unpaired_r += 1
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if unpaired_r > maxseq // 2:
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continue
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msa1.append(msas_i[0])
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msa2.append(msas_i[1])
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else:
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print ("Len error",filename, len(msas_i[0]),len(msa1[0]),len(msas_i[1]),len(msas_i[1]))
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if (len(msa1) >= maxseq):
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break
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# convert letters into numbers
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alphabet = np.array(list("ARNDCQEGHILKMFPSTWYV-Xacgtxbdhuy"), dtype='|S1').view(np.uint8)
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msa1 = np.array([list(s) for s in msa1], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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msa1[msa1 == alphabet[i]] = i
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msa1[msa1>=31] = 21 # anything unknown to 'X'
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alphabet = np.array(list("00000000000000000000-000000ACGTN"), dtype='|S1').view(np.uint8)
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msa2 = np.array([list(s) for s in msa2], dtype='|S1').view(np.uint8)
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for i in range(alphabet.shape[0]):
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msa2[msa2 == alphabet[i]] = i
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msa2[msa2>=31] = 30 # anything unknown to 'N'
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msa = np.concatenate((msa1,msa2),axis=-1)
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ins = np.zeros(msa.shape, dtype=np.uint8)
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return msa,ins
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# read A3M and convert letters into
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# integers in the 0..20 range,
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# also keep track of insertions
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def parse_a3m(filename, maxseq=8000, paired=False):
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msa = []
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ins = []
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taxIDs = []
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table = str.maketrans(dict.fromkeys(string.ascii_lowercase))
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# read file line by line
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if filename.split('.')[-1] == 'gz':
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fstream = gzip.open(filename, 'rt')
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else:
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fstream = open(filename, 'r')
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for i, line in enumerate(fstream):
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# skip labels
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if line[0] == '>':
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if paired: # paired MSAs only have a TAXID in the fasta header
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taxIDs.append(line[1:].strip())
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else: # unpaired MSAs have all the metadata so use regex to pull out TAXID
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if i == 0:
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taxIDs.append("query")
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else:
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match = re.search( r'TaxID=(\d+)', line)
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if match:
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taxIDs.append(match.group(1))
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else:
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taxIDs.append("") # query sequence
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continue
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# remove right whitespaces
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line = line.rstrip()
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if len(line) == 0:
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continue
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# remove lowercase letters and append to MSA
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msa.append(line.translate(table))
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# sequence length
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L = len(msa[-1])
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# 0 - match or gap; 1 - insertion
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a = np.array([0 if c.isupper() or c=='-' else 1 for c in line])
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i = np.zeros((L))
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if np.sum(a) > 0:
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# positions of insertions
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pos = np.where(a==1)[0]
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# shift by occurrence
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a = pos - np.arange(pos.shape[0])
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# position of insertions in cleaned sequence
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# and their length
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pos,num = np.unique(a, return_counts=True)
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# append to the matrix of insetions
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i[pos] = num
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ins.append(i)
|
|
|
|
if (len(msa) >= maxseq):
|
|
break
|
|
|
|
# convert letters into numbers
|
|
alphabet = np.array(list("ARNDCQEGHILKMFPSTWYV-"), dtype='|S1').view(np.uint8)
|
|
msa = np.array([list(s) for s in msa], dtype='|S1').view(np.uint8)
|
|
for i in range(alphabet.shape[0]):
|
|
msa[msa == alphabet[i]] = i
|
|
|
|
# treat all unknown characters as gaps
|
|
msa[msa > 20] = 20
|
|
|
|
ins = np.array(ins, dtype=np.uint8)
|
|
|
|
return msa,ins, np.array(taxIDs)
|
|
|
|
|
|
# read and extract xyz coords of N,Ca,C atoms
|
|
# from a PDB file
|
|
def parse_pdb(filename, seq=False, lddt_mask=False):
|
|
lines = open(filename,'r').readlines()
|
|
if seq:
|
|
return parse_pdb_lines_w_seq(lines, lddt_mask=lddt_mask)
|
|
return parse_pdb_lines(lines)
|
|
|
|
def parse_pdb_lines_w_seq(lines, lddt_mask=False):
|
|
|
|
# indices of residues observed in the structure
|
|
res = [(l[21:22].strip(), l[22:26],l[17:20], l[60:66].strip()) for l in lines if l[:4]=="ATOM" and l[12:16].strip() in ["CA", "P"]] # (chain letter, res num, aa)
|
|
pdb_idx_s = [(r[0], int(r[1])) for r in res]
|
|
idx_s = [int(r[1]) for r in res]
|
|
plddt = [float(r[3]) for r in res]
|
|
seq = [ChemData().aa2num[r[2]] if r[2] in ChemData().aa2num.keys() else 20 for r in res]
|
|
|
|
# 4 BB + up to 10 SC atoms
|
|
xyz = np.full((len(idx_s), ChemData().NTOTAL, 3), np.nan, dtype=np.float32)
|
|
for l in lines:
|
|
if l[:4] != "ATOM":
|
|
continue
|
|
chain, resNo, atom, aa = l[21:22].strip(), int(l[22:26]), l[12:16], l[17:20]
|
|
idx = pdb_idx_s.index((chain,resNo))
|
|
for i_atm, tgtatm in enumerate(ChemData().aa2long[ChemData().aa2num[aa]]):
|
|
if tgtatm == atom:
|
|
xyz[idx,i_atm,:] = [float(l[30:38]), float(l[38:46]), float(l[46:54])]
|
|
break
|
|
|
|
# save atom mask
|
|
mask = np.logical_not(np.isnan(xyz[...,0]))
|
|
xyz[np.isnan(xyz[...,0])] = 0.0
|
|
if lddt_mask == True:
|
|
plddt = np.array(plddt)
|
|
mask_lddt = np.full_like(mask, False)
|
|
mask_lddt[plddt > .85, 5:] = True
|
|
mask_lddt[plddt > .70, :5] = True
|
|
mask = np.logical_and(mask, mask_lddt)
|
|
|
|
return xyz,mask,np.array(idx_s), np.array(seq)
|
|
|
|
#'''
|
|
def parse_pdb_lines(lines):
|
|
|
|
# indices of residues observed in the structure
|
|
res = [(l[21:22].strip(), l[22:26],l[17:20], l[60:66].strip()) for l in lines if l[:4]=="ATOM" and l[12:16].strip() in ["CA", "P"]] # (chain letter, res num, aa)
|
|
pdb_idx_s = [(r[0], int(r[1])) for r in res]
|
|
idx_s = [int(r[1]) for r in res]
|
|
|
|
# 4 BB + up to 10 SC atoms
|
|
xyz = np.full((len(idx_s), ChemData().NTOTAL, 3), np.nan, dtype=np.float32)
|
|
for l in lines:
|
|
if l[:4] != "ATOM":
|
|
continue
|
|
chain, resNo, atom, aa = l[21:22].strip(), int(l[22:26]), l[12:16], l[17:20]
|
|
idx = pdb_idx_s.index((chain,resNo))
|
|
for i_atm, tgtatm in enumerate(ChemData().aa2long[ChemData().aa2num[aa]]):
|
|
if tgtatm == atom:
|
|
xyz[idx,i_atm,:] = [float(l[30:38]), float(l[38:46]), float(l[46:54])]
|
|
break
|
|
|
|
# save atom mask
|
|
mask = np.logical_not(np.isnan(xyz[...,0]))
|
|
xyz[np.isnan(xyz[...,0])] = 0.0
|
|
|
|
return xyz,mask,np.array(idx_s)
|
|
|
|
|
|
def parse_templates(item, params):
|
|
|
|
# init FFindexDB of templates
|
|
### and extract template IDs
|
|
### present in the DB
|
|
ffdb = FFindexDB(read_index(params['FFDB']+'_pdb.ffindex'),
|
|
read_data(params['FFDB']+'_pdb.ffdata'))
|
|
#ffids = set([i.name for i in ffdb.index])
|
|
|
|
# process tabulated hhsearch output to get
|
|
# matched positions and positional scores
|
|
infile = params['DIR']+'/hhr/'+item[-2:]+'/'+item+'.atab'
|
|
hits = []
|
|
for l in open(infile, "r").readlines():
|
|
if l[0]=='>':
|
|
key = l[1:].split()[0]
|
|
hits.append([key,[],[]])
|
|
elif "score" in l or "dssp" in l:
|
|
continue
|
|
else:
|
|
hi = l.split()[:5]+[0.0,0.0,0.0]
|
|
hits[-1][1].append([int(hi[0]),int(hi[1])])
|
|
hits[-1][2].append([float(hi[2]),float(hi[3]),float(hi[4])])
|
|
|
|
# get per-hit statistics from an .hhr file
|
|
# (!!! assume that .hhr and .atab have the same hits !!!)
|
|
# [Probab, E-value, Score, Aligned_cols,
|
|
# Identities, Similarity, Sum_probs, Template_Neff]
|
|
lines = open(infile[:-4]+'hhr', "r").readlines()
|
|
pos = [i+1 for i,l in enumerate(lines) if l[0]=='>']
|
|
for i,posi in enumerate(pos):
|
|
hits[i].append([float(s) for s in re.sub('[=%]',' ',lines[posi]).split()[1::2]])
|
|
|
|
# parse templates from FFDB
|
|
for hi in hits:
|
|
#if hi[0] not in ffids:
|
|
# continue
|
|
entry = get_entry_by_name(hi[0], ffdb.index)
|
|
if entry == None:
|
|
continue
|
|
data = read_entry_lines(entry, ffdb.data)
|
|
hi += list(parse_pdb_lines(data))
|
|
|
|
# process hits
|
|
counter = 0
|
|
xyz,qmap,mask,f0d,f1d,ids = [],[],[],[],[],[]
|
|
for data in hits:
|
|
if len(data)<7:
|
|
continue
|
|
|
|
qi,ti = np.array(data[1]).T
|
|
_,sel1,sel2 = np.intersect1d(ti, data[6], return_indices=True)
|
|
ncol = sel1.shape[0]
|
|
if ncol < 10:
|
|
continue
|
|
|
|
ids.append(data[0])
|
|
f0d.append(data[3])
|
|
f1d.append(np.array(data[2])[sel1])
|
|
xyz.append(data[4][sel2])
|
|
mask.append(data[5][sel2])
|
|
qmap.append(np.stack([qi[sel1]-1,[counter]*ncol],axis=-1))
|
|
counter += 1
|
|
|
|
xyz = np.vstack(xyz).astype(np.float32)
|
|
mask = np.vstack(mask).astype(bool)
|
|
qmap = np.vstack(qmap).astype(np.long)
|
|
f0d = np.vstack(f0d).astype(np.float32)
|
|
f1d = np.vstack(f1d).astype(np.float32)
|
|
ids = ids
|
|
|
|
return xyz,mask,qmap,f0d,f1d,ids
|
|
|
|
def parse_templates_raw(ffdb, hhr_fn, atab_fn, max_templ=20):
|
|
# process tabulated hhsearch output to get
|
|
# matched positions and positional scores
|
|
hits = []
|
|
for l in open(atab_fn, "r").readlines():
|
|
if l[0]=='>':
|
|
if len(hits) == max_templ:
|
|
break
|
|
key = l[1:].split()[0]
|
|
hits.append([key,[],[]])
|
|
elif "score" in l or "dssp" in l:
|
|
continue
|
|
else:
|
|
hi = l.split()[:5]+[0.0,0.0,0.0]
|
|
hits[-1][1].append([int(hi[0]),int(hi[1])])
|
|
hits[-1][2].append([float(hi[2]),float(hi[3]),float(hi[4])])
|
|
|
|
# get per-hit statistics from an .hhr file
|
|
# (!!! assume that .hhr and .atab have the same hits !!!)
|
|
# [Probab, E-value, Score, Aligned_cols,
|
|
# Identities, Similarity, Sum_probs, Template_Neff]
|
|
lines = open(hhr_fn, "r").readlines()
|
|
pos = [i+1 for i,l in enumerate(lines) if l[0]=='>']
|
|
for i,posi in enumerate(pos[:len(hits)]):
|
|
hits[i].append([float(s) for s in re.sub('[=%]',' ',lines[posi]).split()[1::2]])
|
|
|
|
# parse templates from FFDB
|
|
for hi in hits:
|
|
#if hi[0] not in ffids:
|
|
# continue
|
|
entry = get_entry_by_name(hi[0], ffdb.index)
|
|
if entry == None:
|
|
print ("Failed to find %s in *_pdb.ffindex"%hi[0])
|
|
continue
|
|
data = read_entry_lines(entry, ffdb.data)
|
|
hi += list(parse_pdb_lines_w_seq(data))
|
|
|
|
# process hits
|
|
counter = 0
|
|
xyz,qmap,mask,f0d,f1d,ids,seq = [],[],[],[],[],[],[]
|
|
for data in hits:
|
|
if len(data)<7:
|
|
continue
|
|
# print ("Process %s..."%data[0])
|
|
|
|
qi,ti = np.array(data[1]).T
|
|
_,sel1,sel2 = np.intersect1d(ti, data[6], return_indices=True)
|
|
ncol = sel1.shape[0]
|
|
if ncol < 10:
|
|
continue
|
|
|
|
ids.append(data[0])
|
|
f0d.append(data[3])
|
|
f1d.append(np.array(data[2])[sel1])
|
|
xyz.append(data[4][sel2])
|
|
mask.append(data[5][sel2])
|
|
seq.append(data[-1][sel2])
|
|
qmap.append(np.stack([qi[sel1]-1,[counter]*ncol],axis=-1))
|
|
counter += 1
|
|
|
|
xyz = np.vstack(xyz).astype(np.float32)
|
|
mask = np.vstack(mask).astype(bool)
|
|
qmap = np.vstack(qmap).astype(np.int64)
|
|
f0d = np.vstack(f0d).astype(np.float32)
|
|
f1d = np.vstack(f1d).astype(np.float32)
|
|
seq = np.hstack(seq).astype(np.int64)
|
|
ids = ids
|
|
|
|
return torch.from_numpy(xyz), torch.from_numpy(mask), torch.from_numpy(qmap), \
|
|
torch.from_numpy(f0d), torch.from_numpy(f1d), torch.from_numpy(seq), ids
|
|
|
|
def read_templates(qlen, ffdb, hhr_fn, atab_fn, n_templ=10):
|
|
xyz_t, mask_t, qmap, t1d, seq, ids = parse_templates_raw(ffdb, hhr_fn, atab_fn, max_templ=max(n_templ, 20))
|
|
ntmplatoms = xyz_t.shape[1]
|
|
|
|
npick = min(n_templ, len(ids))
|
|
if npick < 1: # no templates
|
|
xyz = torch.full((1,qlen,ChemData().NTOTAL,3),np.nan).float()
|
|
mask = torch.full((1,qlen,ChemData().NTOTAL),False)
|
|
t1d = torch.nn.functional.one_hot(torch.full((1, qlen), 20).long(), num_classes=21).float() # all gaps
|
|
t1d = torch.cat((t1d, torch.zeros((1,qlen,1)).float()), -1)
|
|
return xyz, mask, t1d
|
|
|
|
sample = torch.arange(npick)
|
|
#
|
|
xyz = torch.full((npick, qlen, ChemData().NTOTAL, 3), np.nan).float()
|
|
mask = torch.full((npick, qlen, ChemData().NTOTAL), False)
|
|
f1d = torch.full((npick, qlen), 20).long()
|
|
f1d_val = torch.zeros((npick, qlen, 1)).float()
|
|
#
|
|
for i, nt in enumerate(sample):
|
|
sel = torch.where(qmap[:,1] == nt)[0]
|
|
pos = qmap[sel, 0]
|
|
xyz[i, pos] = xyz_t[sel]
|
|
mask[i, pos, :ntmplatoms] = mask_t[sel].bool()
|
|
f1d[i, pos] = seq[sel]
|
|
f1d_val[i,pos] = t1d[sel, 2].unsqueeze(-1)
|
|
xyz[i] = util.center_and_realign_missing(xyz[i], mask[i], seq=f1d[i])
|
|
|
|
f1d = torch.nn.functional.one_hot(f1d, num_classes=ChemData().NAATOKENS-1).float()
|
|
f1d = torch.cat((f1d, f1d_val), dim=-1)
|
|
|
|
return xyz, mask, f1d
|
|
|
|
|
|
def clean_sdffile(filename):
|
|
# lowercase the 2nd letter of the element name (e.g. FE->Fe) so openbabel can parse it correctly
|
|
lines2 = []
|
|
with open(filename) as f:
|
|
lines = f.readlines()
|
|
num_atoms = int(lines[3][:3])
|
|
for i in range(len(lines)):
|
|
if i>=4 and i<4+num_atoms:
|
|
lines2.append(lines[i][:32]+lines[i][32].lower()+lines[i][33:])
|
|
else:
|
|
lines2.append(lines[i])
|
|
molstring = ''.join(lines2)
|
|
|
|
return molstring
|
|
|
|
def parse_mol(filename, filetype="mol2", string=False, remove_H=True, find_automorphs=True, generate_conformer: bool = False):
|
|
"""Parse small molecule ligand.
|
|
|
|
Parameters
|
|
----------
|
|
filename : str
|
|
filetype : str
|
|
string : bool
|
|
If True, `filename` is a string containing the molecule data.
|
|
remove_H : bool
|
|
Whether to remove hydrogen atoms.
|
|
find_automorphs : bool
|
|
Whether to enumerate atom symmetry permutations.
|
|
|
|
Returns
|
|
-------
|
|
obmol : OBMol
|
|
openbabel molecule object representing the ligand
|
|
msa : torch.Tensor (N_atoms,) long
|
|
Integer-encoded "sequence" (atom types) of ligand
|
|
ins : torch.Tensor (N_atoms,) long
|
|
Insertion features (all zero) for RF input
|
|
atom_coords : torch.Tensor (N_symmetry, N_atoms, 3) float
|
|
Atom coordinates
|
|
mask : torch.Tensor (N_symmetry, N_atoms) bool
|
|
Boolean mask for whether atom exists
|
|
"""
|
|
obConversion = openbabel.OBConversion()
|
|
obConversion.SetInFormat(filetype)
|
|
obmol = openbabel.OBMol()
|
|
if string:
|
|
obConversion.ReadString(obmol,filename)
|
|
elif filetype=='sdf':
|
|
molstring = clean_sdffile(filename)
|
|
obConversion.ReadString(obmol,molstring)
|
|
else:
|
|
obConversion.ReadFile(obmol,filename)
|
|
if generate_conformer:
|
|
builder = openbabel.OBBuilder()
|
|
builder.Build(obmol)
|
|
ff = openbabel.OBForceField.FindForceField("mmff94")
|
|
did_setup = ff.Setup(obmol)
|
|
if did_setup:
|
|
ff.FastRotorSearch()
|
|
ff.GetCoordinates(obmol)
|
|
else:
|
|
raise ValueError(f"Failed to generate 3D coordinates for molecule {filename}.")
|
|
if remove_H:
|
|
obmol.DeleteHydrogens()
|
|
# the above sometimes fails to get all the hydrogens
|
|
i = 1
|
|
while i < obmol.NumAtoms()+1:
|
|
if obmol.GetAtom(i).GetAtomicNum()==1:
|
|
obmol.DeleteAtom(obmol.GetAtom(i))
|
|
else:
|
|
i += 1
|
|
atomtypes = [ChemData().atomnum2atomtype.get(obmol.GetAtom(i).GetAtomicNum(), 'ATM')
|
|
for i in range(1, obmol.NumAtoms()+1)]
|
|
msa = torch.tensor([ChemData().aa2num[x] for x in atomtypes])
|
|
ins = torch.zeros_like(msa)
|
|
|
|
atom_coords = torch.tensor([[obmol.GetAtom(i).x(),obmol.GetAtom(i).y(), obmol.GetAtom(i).z()]
|
|
for i in range(1, obmol.NumAtoms()+1)]).unsqueeze(0) # (1, natoms, 3)
|
|
mask = torch.full(atom_coords.shape[:-1], True) # (1, natoms,)
|
|
|
|
if find_automorphs:
|
|
atom_coords, mask = util.get_automorphs(obmol, atom_coords[0], mask[0])
|
|
|
|
return obmol, msa, ins, atom_coords, mask
|