{"title":"GMSF: A Dual-Path Multimodal Framework for Enzyme Function Prediction via Difference Graph Encoding and Multiscale Semantic Fusion","authors":"Xin Zhao, Haoshu Chen, Tao Zhang, Yahui Cao, Haotong Li, Zhuoran Song, Bingzhi Li, Shuo Zheng","doi":"10.1021/acs.jcim.6c02672","DOIUrl":null,"url":null,"abstract":"<p>Enzymes play a central role in green chemistry and biomanufacturing.\r\nHowever, precise enzyme selection via Enzyme Commission (EC) number\r\nprediction remains a critical bottleneck between the retrosynthetic\r\npathway planning and experimental implementation. Existing computational\r\nmethods predominantly rely on single-modality representations that\r\neither lose spatial topological structures or treat reactions as static\r\nsnapshots, failing to capture the explicit atom-level state transitions\r\nin chemical bond evolution. To address these limitations, we propose\r\nGMSF, a dual-path multimodal deep learning framework. GMSF features\r\ntwo core innovations: Difference Graph Encoding, which leverages atom–atom\r\nmapping (AAM) to compute node feature differences and extract structural\r\ndifference signatures of reaction centers; and Multiscale Sequence\r\nEncoding, which uses AAM-aligned node mappings to hierarchically capture\r\nchemical semantics. Experimental results on the ECREACT dataset demonstrate\r\nthat GMSF achieves an accuracy of 93.17% in the highly challenging\r\nlevel 3 (subsubclass) enzyme function prediction, outperforming the\r\nstate-of-the-art (SOTA) baseline by a margin of 1.36%. Furthermore,\r\nits successful application to real-world metabolic networks in the\r\nBioCyc database validates its immense potential for deciphering complex\r\nbiochemical reactions, serving as a powerful computational screening\r\ntool to narrow down catalytic mechanisms and coenzyme dependencies\r\nprior to the exact enzyme selection.</p>","PeriodicalId":44,"journal":{"name":"Journal of Chemical Information and Modeling ","volume":"66 19","pages":"12904–12918"},"PeriodicalIF":6.4000,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Information and Modeling ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jcim.6c02672","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/30 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Enzymes play a central role in green chemistry and biomanufacturing.
However, precise enzyme selection via Enzyme Commission (EC) number
prediction remains a critical bottleneck between the retrosynthetic
pathway planning and experimental implementation. Existing computational
methods predominantly rely on single-modality representations that
either lose spatial topological structures or treat reactions as static
snapshots, failing to capture the explicit atom-level state transitions
in chemical bond evolution. To address these limitations, we propose
GMSF, a dual-path multimodal deep learning framework. GMSF features
two core innovations: Difference Graph Encoding, which leverages atom–atom
mapping (AAM) to compute node feature differences and extract structural
difference signatures of reaction centers; and Multiscale Sequence
Encoding, which uses AAM-aligned node mappings to hierarchically capture
chemical semantics. Experimental results on the ECREACT dataset demonstrate
that GMSF achieves an accuracy of 93.17% in the highly challenging
level 3 (subsubclass) enzyme function prediction, outperforming the
state-of-the-art (SOTA) baseline by a margin of 1.36%. Furthermore,
its successful application to real-world metabolic networks in the
BioCyc database validates its immense potential for deciphering complex
biochemical reactions, serving as a powerful computational screening
tool to narrow down catalytic mechanisms and coenzyme dependencies
prior to the exact enzyme selection.
期刊介绍:
The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery.
Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field.
As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.