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d0d761f | 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 | # src/applicability_domain.py
#
# Three-layer applicability domain check.
# Flags garbage inputs before prediction is shown to the user.
#
# Layer 1 β Sequence sanity (catches poly-A, random chars, empty)
# Layer 2 β Ligand sanity (catches invalid SMILES, non-drug-like)
# Layer 3 β Embedding AD (catches proteins far from training dist)
import numpy as np
from collections import Counter
from rdkit import Chem
from rdkit.Chem import Descriptors
from rdkit import RDLogger
RDLogger.DisableLog('rdApp.*')
STANDARD_AA = set('ACDEFGHIKLMNPQRSTVWY')
# ββ Layer 1: Sequence βββββββββββββββββββββββββββββββββββββββββββββββββ
def check_sequence(seq: str) -> tuple:
"""Returns (score 0-100, list of warning strings)."""
seq = seq.strip().upper()
warn = []
if not seq:
return 0.0, ["EMPTY_SEQUENCE"]
invalid_frac = sum(1 for c in seq if c not in STANDARD_AA) / len(seq)
if invalid_frac > 0.30:
return 0.0, [f"NOT_A_PROTEIN: {invalid_frac:.0%} non-standard characters"]
clean = ''.join(c for c in seq if c in STANDARD_AA)
if not clean:
return 0.0, ["NOT_A_PROTEIN: no standard amino acids found"]
score = 100.0
# Low complexity (poly-X)
counts = Counter(clean)
top_frac = counts.most_common(1)[0][1] / len(clean)
if top_frac > 0.40:
warn.append(f"LOW_COMPLEXITY: single AA = {top_frac:.0%} of sequence "
f"(likely poly-X repeat β prediction unreliable)")
score -= 50
# Shannon entropy
freqs = np.array(list(counts.values())) / len(clean)
entropy = -np.sum(freqs * np.log2(freqs + 1e-10))
if entropy < 2.5:
warn.append(f"LOW_ENTROPY: {entropy:.2f} bits β low complexity sequence")
score -= 25
# Unique AAs
if len(counts) < 5:
warn.append(f"LOW_DIVERSITY: only {len(counts)} unique amino acids")
score -= 25
if len(seq) < 50:
warn.append(f"SHORT: length {len(seq)} β may be a peptide, not a drug target")
score -= 15
if invalid_frac > 0:
warn.append(f"NON_STANDARD: {invalid_frac:.0%} non-standard characters present")
score -= 10
return max(0.0, score), warn
# ββ Layer 2: Ligand βββββββββββββββββββββββββββββββββββββββββββββββββββ
def check_ligand(smiles: str) -> tuple:
"""Returns (score 0-100, list of warning strings)."""
warn = []
if not smiles or not smiles.strip():
return 0.0, ["EMPTY_SMILES"]
mol = Chem.MolFromSmiles(smiles.strip())
if mol is None:
return 0.0, ["INVALID_SMILES: RDKit could not parse this string"]
score = 100.0
mw = Descriptors.MolWt(mol)
if mw < 100:
warn.append(f"LOW_MW: {mw:.1f} Da β likely a fragment or solvent")
score -= 40
elif mw > 1000:
warn.append(f"HIGH_MW: {mw:.1f} Da β may be outside training distribution")
score -= 20
n_heavy = mol.GetNumHeavyAtoms()
if n_heavy < 5:
warn.append(f"TOO_SMALL: only {n_heavy} heavy atoms")
score -= 40
allowed = {1, 5, 6, 7, 8, 9, 14, 15, 16, 17, 35, 53}
exotic = {a.GetSymbol() for a in mol.GetAtoms()
if a.GetAtomicNum() not in allowed and a.GetAtomicNum() != 0}
if exotic:
warn.append(f"EXOTIC_ATOMS: {', '.join(sorted(exotic))} β rare in training data")
score -= 20
return max(0.0, score), warn
# ββ Layer 3: Embedding AD βββββββββββββββββββββββββββββββββββββββββββββ
class EmbeddingAD:
"""
kNN applicability domain in ESM embedding space.
Flags proteins far from the training distribution.
"""
def __init__(self, k: int = 5, percentile: float = 95.0):
self.k = k
self.percentile = percentile
self.fitted = False
def fit(self, train_embeddings: np.ndarray):
from sklearn.neighbors import NearestNeighbors
print(f"Fitting Embedding AD on {len(train_embeddings)} proteins...")
self.nn = NearestNeighbors(n_neighbors=self.k + 1,
metric='cosine', n_jobs=-1)
self.nn.fit(train_embeddings.astype(np.float32))
dists, _ = self.nn.kneighbors(train_embeddings.astype(np.float32))
knn_dists = dists[:, 1:].mean(axis=1)
self.threshold = np.percentile(knn_dists, self.percentile)
self.fitted = True
print(f" AD threshold ({self.percentile}th pct): {self.threshold:.4f}")
return self
def score(self, embedding: np.ndarray) -> tuple:
"""Returns (distance, score 0-100, in_domain bool)."""
if not self.fitted:
return None, 100.0, True
dists, _ = self.nn.kneighbors(
embedding.reshape(1, -1).astype(np.float32), n_neighbors=self.k
)
dist = float(dists[0].mean())
in_domain = dist <= self.threshold
if dist <= self.threshold:
ad_score = 50 + 50 * (1 - dist / self.threshold)
else:
ad_score = max(0.0, 50 * (1 - (dist - self.threshold) / self.threshold))
return dist, ad_score, in_domain
# ββ Combined report βββββββββββββββββββββββββββββββββββββββββββββββββββ
def confidence_report(seq: str, smiles: str,
embedding: np.ndarray = None,
ad_model: EmbeddingAD = None) -> dict:
seq_score, seq_warn = check_sequence(seq)
lig_score, lig_warn = check_ligand(smiles)
ad_score, ad_dist, in_domain = 100.0, None, True
if embedding is not None and ad_model is not None:
ad_dist, ad_score, in_domain = ad_model.score(embedding)
if not in_domain:
seq_warn.append(
f"OUT_OF_DOMAIN: protein distance={ad_dist:.3f} "
f"(threshold={ad_model.threshold:.3f})"
)
all_warn = seq_warn + lig_warn
w_ad = 0.20 if ad_model else 0.0
w_seq = 0.55 if not ad_model else 0.45
w_lig = 1.0 - w_seq - w_ad
overall = w_seq * seq_score + w_lig * lig_score + w_ad * ad_score
if overall >= 70 and seq_score >= 60 and lig_score >= 60:
flag = 'RELIABLE'
elif overall >= 40:
flag = 'UNCERTAIN'
else:
flag = 'UNRELIABLE'
return {
'flag': flag,
'overall': round(overall, 1),
'seq_score': round(seq_score, 1),
'lig_score': round(lig_score, 1),
'ad_score': round(ad_score, 1),
'in_domain': in_domain,
'warnings': all_warn,
}
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