MINT: Predicting Enzyme-Cofactor Specificity by Multimodal Knowledge Transfer from Protein-Ligand Interactions

Protein-cofactor selectivity prediction is important for enzyme annotation, metabolic engineering, and biocatalyst discovery, but it remains challenging because experimentally supported associations are limited and unevenly distributed, and because biologically relevant differences can be subtler than those captured by general protein-ligand interaction models. Here, we present MINT (Multimodal Interaction Network with Teacher supervision), a multimodal framework for cofactor specificity prediction. MINT combines protein sequence features with cofactor sequence and graph representations and is trained with a gradual adaptation strategy that transfers useful information from a pretrained protein-ligand interaction model to the cofactor prediction task. On a fixed balanced held-out test set, MINT achieved the best overall performance among all compared methods (AUC = 0.932), and this ranking was reproduced in an independent family-stratified evaluation at the natural positive rate (pooled AUC = 0.939). Further analyses suggest that the pretrained model provides transferable structural information, while the gradual training scheme helps adapt that information to cofactor specificity. In a case study of the chemically near-identical NAD/NADP pair, MINT recovered 95.0-98.6% of true binders and resolved a single-phosphate-level distinction with direct relevance to engineering enzyme cofactor specificity. These results show that gradual transfer learning is an effective approach to cofactor specificity prediction when annotation is limited.