Evidence map›Paper›PMID 42834449›Full record

ArticleBioinformatics (Oxford, England)2026

Pocket contrastive learning and conformation fusion for robust structure-conditioned 3D molecular generation under receptor conformational variation.

Huan Liu, Yijie Ding, Xiaoyi Guo, Hongjie Wu

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Huan LiuCollege of Electronic and Information Engineering, Suzhou University of Science and Technology, Suzhou, 215009, China.
Yijie DingFaculty of Computing, Harbin Institute of Technology, Harbin, 150001, China.ORCID 0000-0002-3438-9259
Xiaoyi GuoLi Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Hongjie WuCollege of Electronic and Information Engineering, Suzhou University of Science and Technology, Suzhou, 215009, China.ORCID 0000-0001-5921-8707

Funding

National Natural Science Foundation of China 62502334National Natural Science Foundation of China 62506255National Natural Science Foundation of China 62672153
6 · The paper itself

Abstract

motivationPocket-conditioned molecular generation incorporates the three-dimensional (3D) geometry and chemical environment of protein binding sites into molecular design. However, receptor conformational variation can introduce distribution shifts between training and inference, particularly under cross-docking conditions. Existing approaches often do not fully exploit the correspondence between related receptor conformations during training.

resultsWe propose a structure-conditioned 3D molecular generation framework that combines pocket-level contrastive learning with reference-conformation feature fusion. Built on a stepwise constructive generative model, these training-stage components encourage stable pocket representations across related conformations while preserving single-pocket inference without requiring a reference conformation. Evaluation on CrossDocked2020 and three external datasets, ASB-E, DUD-E, and APObind, demonstrates improvements in generation success, structural validity, and docking-related performance, particularly under cross-dock evaluation. These results support improved robustness of pocket-conditioned molecular generation under receptor conformational variation. AVAILABILITY AND IMPLEMENTATION: The source code and reproduction instructions are available at https://github.com/LHHHHuan/MTMGen. Pretrained models and an archival code snapshot are available at https://doi.org/10.5281/zenodo.21944857.

Indexed as

Computational BiologyMachine LearningMolecular Docking SimulationProteinsBinding SitesModels, MolecularProtein ConformationProteins

Identifiers

PMID42834449
PMCPMC13671754

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