TD3B / scoring /functions /binding.py
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import sys
import os, torch
import numpy as np
import torch
import pandas as pd
import torch.nn as nn
import esm
from transformers import AutoModelForMaskedLM
def _sanitize_token_ids(input_ids: torch.Tensor, vocab_size: int, unk_id: int) -> torch.Tensor:
if vocab_size <= 0 or input_ids.numel() == 0:
return input_ids
if torch.any(input_ids >= vocab_size) or torch.any(input_ids < 0):
# Replace out-of-range IDs with UNK to avoid embedding OOB.
unk = torch.tensor(unk_id, device=input_ids.device, dtype=input_ids.dtype)
input_ids = torch.where((input_ids >= vocab_size) | (input_ids < 0), unk, input_ids)
return input_ids
class ImprovedBindingPredictor(nn.Module):
def __init__(self,
esm_dim=1280,
smiles_dim=768,
hidden_dim=512,
n_heads=8,
n_layers=3,
dropout=0.1):
super().__init__()
# Define binding thresholds
self.tight_threshold = 7.5 # Kd/Ki/IC50 ≤ ~30nM
self.weak_threshold = 6.0 # Kd/Ki/IC50 > 1μM
# Project to same dimension
self.smiles_projection = nn.Linear(smiles_dim, hidden_dim)
self.protein_projection = nn.Linear(esm_dim, hidden_dim)
self.protein_norm = nn.LayerNorm(hidden_dim)
self.smiles_norm = nn.LayerNorm(hidden_dim)
# Cross attention blocks with layer norm
self.cross_attention_layers = nn.ModuleList([
nn.ModuleDict({
'attention': nn.MultiheadAttention(hidden_dim, n_heads, dropout=dropout),
'norm1': nn.LayerNorm(hidden_dim),
'ffn': nn.Sequential(
nn.Linear(hidden_dim, hidden_dim * 4),
nn.ReLU(),
nn.Dropout(dropout),
nn.Linear(hidden_dim * 4, hidden_dim)
),
'norm2': nn.LayerNorm(hidden_dim)
}) for _ in range(n_layers)
])
# Prediction heads
self.shared_head = nn.Sequential(
nn.Linear(hidden_dim * 2, hidden_dim),
nn.ReLU(),
nn.Dropout(dropout),
)
# Regression head
self.regression_head = nn.Linear(hidden_dim, 1)
# Classification head (3 classes: tight, medium, loose binding)
self.classification_head = nn.Linear(hidden_dim, 3)
def get_binding_class(self, affinity):
"""Convert affinity values to class indices
0: tight binding (>= 7.5)
1: medium binding (6.0-7.5)
2: weak binding (< 6.0)
"""
if isinstance(affinity, torch.Tensor):
tight_mask = affinity >= self.tight_threshold
weak_mask = affinity < self.weak_threshold
medium_mask = ~(tight_mask | weak_mask)
classes = torch.zeros_like(affinity, dtype=torch.long)
classes[medium_mask] = 1
classes[weak_mask] = 2
return classes
else:
if affinity >= self.tight_threshold:
return 0 # tight binding
elif affinity < self.weak_threshold:
return 2 # weak binding
else:
return 1 # medium binding
def forward(self, protein_emb, smiles_emb):
protein = self.protein_norm(self.protein_projection(protein_emb))
smiles = self.smiles_norm(self.smiles_projection(smiles_emb))
#protein = protein.transpose(0, 1)
#smiles = smiles.transpose(0, 1)
# Cross attention layers
for layer in self.cross_attention_layers:
# Protein attending to SMILES
attended_protein = layer['attention'](
protein, smiles, smiles
)[0]
protein = layer['norm1'](protein + attended_protein)
protein = layer['norm2'](protein + layer['ffn'](protein))
# SMILES attending to protein
attended_smiles = layer['attention'](
smiles, protein, protein
)[0]
smiles = layer['norm1'](smiles + attended_smiles)
smiles = layer['norm2'](smiles + layer['ffn'](smiles))
# Get sequence-level representations
protein_pool = torch.mean(protein, dim=0)
smiles_pool = torch.mean(smiles, dim=0)
# Concatenate both representations
combined = torch.cat([protein_pool, smiles_pool], dim=-1)
# Shared features
shared_features = self.shared_head(combined)
regression_output = self.regression_head(shared_features)
classification_logits = self.classification_head(shared_features)
return regression_output, classification_logits
class BindingAffinity:
def __init__(self, prot_seq, tokenizer, base_path, device=None, emb_model=None):
super().__init__()
self.device = torch.device("cuda" if torch.cuda.is_available() else "cpu") if device is None else device
# peptide embeddings
if emb_model is not None:
self.pep_model = emb_model.to(self.device).eval()
else:
self.pep_model = AutoModelForMaskedLM.from_pretrained('aaronfeller/PeptideCLM-23M-all').roformer.to(self.device).eval()
self.pep_tokenizer = tokenizer
self.unk_id = getattr(self.pep_tokenizer, "unk_token_id", None)
if self.unk_id is None:
self.unk_id = self.pep_tokenizer.vocab.get(self.pep_tokenizer.unk_token, 0)
self.pep_vocab_size = None
self.max_pep_len = None
if hasattr(self.pep_model, "model") and hasattr(self.pep_model.model, "roformer"):
self.pep_vocab_size = self.pep_model.model.roformer.embeddings.word_embeddings.num_embeddings
self.max_pep_len = self.pep_model.model.roformer.config.max_position_embeddings
elif hasattr(self.pep_model, "roformer"):
self.pep_vocab_size = self.pep_model.roformer.embeddings.word_embeddings.num_embeddings
self.max_pep_len = self.pep_model.roformer.config.max_position_embeddings
elif hasattr(self.pep_model, "get_input_embeddings"):
self.pep_vocab_size = self.pep_model.get_input_embeddings().num_embeddings
self.max_pep_len = getattr(self.pep_model.config, "max_position_embeddings", None)
self.model = ImprovedBindingPredictor().to(self.device)
checkpoint = torch.load(f'{base_path}/tr2d2-pep/scoring/functions/classifiers/binding-affinity.pt',
map_location=self.device,
weights_only=False)
self.model.load_state_dict(checkpoint['model_state_dict'])
self.model.eval()
self.esm_model, alphabet = esm.pretrained.esm2_t33_650M_UR50D() # load ESM-2 model
self.esm_model = self.esm_model.to(self.device).eval()
self.prot_tokenizer = alphabet.get_batch_converter() # load esm tokenizer
data = [("target", prot_seq)]
# get tokenized protein
_, _, prot_tokens = self.prot_tokenizer(data)
prot_tokens = prot_tokens.to(self.device)
with torch.no_grad():
results = self.esm_model.forward(prot_tokens, repr_layers=[33]) # Example with ESM-2
prot_emb = results["representations"][33]
self.prot_emb = prot_emb[0].to(self.device)
self.prot_emb = torch.mean(self.prot_emb, dim=0, keepdim=True)
def forward(self, input_seqs):
with torch.no_grad():
scores = []
for seq in input_seqs:
pep_tokens = self.pep_tokenizer(
seq,
return_tensors='pt',
padding=True,
truncation=self.max_pep_len is not None,
max_length=self.max_pep_len,
)
pep_tokens = {k: v.to(self.device) for k, v in pep_tokens.items()}
pep_tokens["input_ids"] = _sanitize_token_ids(
pep_tokens["input_ids"], int(self.pep_vocab_size or 0), int(self.unk_id)
)
with torch.no_grad():
# Check if using custom Roformer wrapper or standard model
if hasattr(self.pep_model, 'model'):
# Custom roformer.Roformer wrapper - get hidden states from inner model
emb = self.pep_model.model.roformer(
input_ids=pep_tokens['input_ids'],
attention_mask=pep_tokens.get('attention_mask'),
output_hidden_states=True
)
pep_emb = emb.last_hidden_state.squeeze(0)
pep_emb = torch.mean(pep_emb, dim=0, keepdim=True)
else:
# Standard AutoModelForMaskedLM
emb = self.pep_model(
input_ids=pep_tokens['input_ids'],
attention_mask=pep_tokens.get('attention_mask'),
output_hidden_states=True
)
pep_emb = emb.last_hidden_state.squeeze(0)
pep_emb = torch.mean(pep_emb, dim=0, keepdim=True)
score, logits = self.model.forward(self.prot_emb, pep_emb)
scores.append(score.item())
return scores
def __call__(self, input_seqs: list):
return self.forward(input_seqs)
class MultiTargetBindingAffinity:
"""
Binding affinity predictor that can handle multiple protein targets dynamically.
Unlike BindingAffinity which pre-computes a single target's embedding,
this class can switch between different protein targets on-the-fly.
"""
def __init__(self, tokenizer, base_path, device=None, emb_model=None):
"""
Initialize multi-target binding affinity predictor.
Args:
tokenizer: Peptide tokenizer
base_path: Base path for model files
device: Device for computation (default: auto-detect)
emb_model: Optional pre-loaded embedding model
"""
super().__init__()
self.device = torch.device("cuda" if torch.cuda.is_available() else "cpu") if device is None else device
# Peptide embeddings
if emb_model is not None:
self.pep_model = emb_model.to(self.device).eval()
else:
self.pep_model = AutoModelForMaskedLM.from_pretrained('aaronfeller/PeptideCLM-23M-all').roformer.to(self.device).eval()
self.pep_tokenizer = tokenizer
self.unk_id = getattr(self.pep_tokenizer, "unk_token_id", None)
if self.unk_id is None:
self.unk_id = self.pep_tokenizer.vocab.get(self.pep_tokenizer.unk_token, 0)
self.pep_vocab_size = None
self.max_pep_len = None
if hasattr(self.pep_model, "model") and hasattr(self.pep_model.model, "roformer"):
self.pep_vocab_size = self.pep_model.model.roformer.embeddings.word_embeddings.num_embeddings
self.max_pep_len = self.pep_model.model.roformer.config.max_position_embeddings
elif hasattr(self.pep_model, "roformer"):
self.pep_vocab_size = self.pep_model.roformer.embeddings.word_embeddings.num_embeddings
self.max_pep_len = self.pep_model.roformer.config.max_position_embeddings
elif hasattr(self.pep_model, "get_input_embeddings"):
self.pep_vocab_size = self.pep_model.get_input_embeddings().num_embeddings
self.max_pep_len = getattr(self.pep_model.config, "max_position_embeddings", None)
# Binding affinity prediction model
self.model = ImprovedBindingPredictor().to(self.device)
checkpoint = torch.load(f'{base_path}/tr2d2-pep/scoring/functions/classifiers/binding-affinity.pt',
map_location=self.device,
weights_only=False)
self.model.load_state_dict(checkpoint['model_state_dict'])
self.model.eval()
# Protein (ESM) model
self.esm_model, alphabet = esm.pretrained.esm2_t33_650M_UR50D()
self.esm_model = self.esm_model.to(self.device).eval()
self.prot_tokenizer = alphabet.get_batch_converter()
# Cache for protein embeddings (target_seq -> embedding)
self.prot_emb_cache = {}
def get_protein_embedding(self, prot_seq: str):
"""
Get protein embedding, using cache if available.
Args:
prot_seq: Protein amino acid sequence
Returns:
Protein embedding tensor
"""
# Check cache first
if prot_seq in self.prot_emb_cache:
return self.prot_emb_cache[prot_seq]
# Compute embedding
data = [("target", prot_seq)]
_, _, prot_tokens = self.prot_tokenizer(data)
prot_tokens = prot_tokens.to(self.device)
with torch.no_grad():
results = self.esm_model.forward(prot_tokens, repr_layers=[33])
prot_emb = results["representations"][33]
prot_emb = prot_emb[0].to(self.device)
prot_emb = torch.mean(prot_emb, dim=0, keepdim=True)
# Cache for future use
self.prot_emb_cache[prot_seq] = prot_emb
return prot_emb
def forward(self, input_seqs, prot_seq: str):
"""
Predict binding affinity for peptide-protein pairs.
Args:
input_seqs: List of peptide sequences
prot_seq: Protein target sequence
Returns:
List of binding affinity scores
"""
# Get protein embedding (cached if previously computed)
prot_emb = self.get_protein_embedding(prot_seq)
with torch.no_grad():
scores = []
for seq in input_seqs:
pep_tokens = self.pep_tokenizer(
seq,
return_tensors='pt',
padding=True,
truncation=self.max_pep_len is not None,
max_length=self.max_pep_len,
)
pep_tokens = {k: v.to(self.device) for k, v in pep_tokens.items()}
pep_tokens["input_ids"] = _sanitize_token_ids(
pep_tokens["input_ids"], int(self.pep_vocab_size or 0), int(self.unk_id)
)
with torch.no_grad():
# Check if using custom Roformer wrapper or standard model
if hasattr(self.pep_model, 'model'):
# Custom roformer.Roformer wrapper - get hidden states from inner model
emb = self.pep_model.model.roformer(
input_ids=pep_tokens['input_ids'],
attention_mask=pep_tokens.get('attention_mask'),
output_hidden_states=True
)
pep_emb = emb.last_hidden_state.squeeze(0)
pep_emb = torch.mean(pep_emb, dim=0, keepdim=True)
else:
# Standard AutoModelForMaskedLM
emb = self.pep_model(
input_ids=pep_tokens['input_ids'],
attention_mask=pep_tokens.get('attention_mask'),
output_hidden_states=True
)
pep_emb = emb.last_hidden_state.squeeze(0)
pep_emb = torch.mean(pep_emb, dim=0, keepdim=True)
score, logits = self.model.forward(prot_emb, pep_emb)
scores.append(score.item())
return scores
def forward_from_probs(
self,
token_probs: torch.Tensor,
attention_mask: torch.Tensor,
prot_seq: str,
) -> torch.Tensor:
"""
Differentiable binding affinity from token probabilities.
"""
if token_probs.dim() == 2:
token_probs = token_probs.unsqueeze(0)
token_probs = token_probs.to(self.device)
attention_mask = attention_mask.to(self.device)
roformer = None
if hasattr(self.pep_model, "model") and hasattr(self.pep_model.model, "roformer"):
roformer = self.pep_model.model.roformer
emb_weight = roformer.embeddings.word_embeddings.weight
elif hasattr(self.pep_model, "roformer"):
roformer = self.pep_model.roformer
emb_weight = roformer.embeddings.word_embeddings.weight
else:
emb_weight = self.pep_model.get_input_embeddings().weight
if token_probs.size(-1) != emb_weight.size(0):
raise ValueError(
f"Token vocab mismatch: probs={token_probs.size(-1)} vs model={emb_weight.size(0)}"
)
inputs_embeds = token_probs @ emb_weight
if roformer is not None:
outputs = roformer(inputs_embeds=inputs_embeds, attention_mask=attention_mask)
hidden = outputs.last_hidden_state
else:
outputs = self.pep_model(
inputs_embeds=inputs_embeds,
attention_mask=attention_mask,
output_hidden_states=True,
return_dict=True,
)
hidden = outputs.hidden_states[-1]
mask = attention_mask.to(hidden.dtype).unsqueeze(-1)
pep_emb = (hidden * mask).sum(dim=1) / mask.sum(dim=1).clamp_min(1.0)
prot_emb = self.get_protein_embedding(prot_seq).to(self.device)
prot_emb = prot_emb.expand(pep_emb.size(0), -1).unsqueeze(0)
pep_emb = pep_emb.unsqueeze(0)
score, _ = self.model.forward(prot_emb, pep_emb)
return score.squeeze(-1)
def __call__(self, input_seqs: list, prot_seq: str):
"""
Predict binding affinity for peptide-protein pairs.
Args:
input_seqs: List of peptide sequences
prot_seq: Protein target sequence
Returns:
List of binding affinity scores
"""
return self.forward(input_seqs, prot_seq)
def clear_cache(self):
"""Clear the protein embedding cache to free memory."""
self.prot_emb_cache = {}
class TargetSpecificBindingAffinity:
"""
Wrapper that binds a specific protein target to MultiTargetBindingAffinity.
This allows using MultiTargetBindingAffinity with the standard BindingAffinity interface
where only peptide sequences need to be provided.
"""
def __init__(self, multi_target_predictor: MultiTargetBindingAffinity, prot_seq: str):
"""
Create a target-specific binding affinity predictor.
Args:
multi_target_predictor: The underlying multi-target predictor
prot_seq: The protein target sequence to use
"""
self.predictor = multi_target_predictor
self.prot_seq = prot_seq
def forward(self, input_seqs):
"""
Predict binding affinity for peptides against the bound target.
Args:
input_seqs: List of peptide sequences
Returns:
List of binding affinity scores
"""
return self.predictor.forward(input_seqs, self.prot_seq)
def __call__(self, input_seqs: list):
"""
Predict binding affinity for peptides against the bound target.
Args:
input_seqs: List of peptide sequences
Returns:
List of binding affinity scores
"""
return self.forward(input_seqs)