{"doi":"10.1101/2025.08.20.671365","title":"ESMDynamic: Fast and Accurate Prediction of Protein Dynamic Contact Maps from Single Sequences","abstract":"Abstract Understanding conformational dynamics is essential for elucidating protein function, yet most deep learning models in structural biology predict only static structures. Here, we present ESMDynamic, a deep learning model that predicts residue–residue contact dynamics directly from protein sequence. Built on the ESMFold architecture and trained on conformational variability from experimental structure ensembles and molecular dynamics (MD) simulations, ESMDynamic predicts dynamic contact probabilities, contact frequencies reflecting equilibrium populations, and coarse-grained kinetics of contact formation and dissociation across multiple temperature conditions. On large-scale MD benchmarks (mdCATH and ATLAS), ESMDynamic matches or outperforms state-of-the-art ensemble prediction methods (AlphaFlow, ESMFlow, BioEmu) while requiring orders-of-magnitude less computation. We demonstrate generalization to diverse systems, including membrane transporters, a de novo designed protein, and a homodimer complex. We show that predicted dynamic contacts enable automated selection of collective variables for Markov state model construction. Applied to the human proteome, ESMDynamic generates predictions for over 18,000 proteins, enabling large-scale analysis of conformational variability. Overall, ESMDynamic provides a scalable, sequence-based representation of protein dynamics to inform simulation, analysis, and design workflows.","journal":"bioRxiv (Cold Spring Harbor Laboratory)","year":2025,"id":555267,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":4,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9437,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2025-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":981418,"name":"Jiangyan Feng","orcid":"0000-0003-0292-6758","position":1,"is_corresponding":false},{"id":5790,"name":"Zhengyuan Xue","orcid":null,"position":2,"is_corresponding":false},{"id":625516,"name":"Diwakar Shukla","orcid":"0000-0003-4079-5381","position":3,"is_corresponding":false},{"id":1453561,"name":"Diego E. Kleiman","orcid":"0000-0002-3833-5872","position":0,"is_corresponding":true}],"reference_count":65,"raw_metadata":null,"created_at":"2026-07-19T02:54:59.329539Z","pmid":"40894558","pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}