Protein Language Model Embeddings Distinguish Catalytic from Structural Zinc-Binding Sites with Interpretable Attention Signatures

Zinc ions serve dual roles in proteins: as catalytic cofactors and as structural elements. Distinguishing these functional classes from sequence alone remains challenging, because both share similar coordination geometries. Here, we demonstrate that ESM-2 embeddings encode sufficient information to classify catalytic versus structural zinc sites with high accuracy. On 73 sequence-diverse zinc proteins, machine learning classifiers achieve ROC-AUC of 0.93-0.97, significantly outperforming a motif-based baseline (AUC = 0.759; <i>p</i> = 0.015). Attention analysis reveals that histidine ligands in catalytic sites attend 9.2-fold more strongly to second-shell carboxylate residues─the proton-shuttling machinery essential for catalysis─than to random positions, providing mechanistic interpretability. These findings suggest that evolutionary sequence patterns encode the extended hydrogen-bonding networks distinguishing catalytic from structural sites. This sequence-only approach complements structure-based methods for large-scale metalloproteome annotation.