File size: 6,927 Bytes
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')


# ── Layer 1: Sequence ─────────────────────────────────────────────────

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


# ── Layer 2: Ligand ───────────────────────────────────────────────────

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


# ── Layer 3: Embedding AD ─────────────────────────────────────────────

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


# ── Combined report ───────────────────────────────────────────────────

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,
    }