AlphaFold2 reveals commonalities and novelties in protein structure space for 21 model organisms

被引:0
作者
Nicola Bordin
Ian Sillitoe
Vamsi Nallapareddy
Clemens Rauer
Su Datt Lam
Vaishali P. Waman
Neeladri Sen
Michael Heinzinger
Maria Littmann
Stephanie Kim
Sameer Velankar
Martin Steinegger
Burkhard Rost
Christine Orengo
机构
[1] University College London,Institute of Structural and Molecular Biology
[2] Universiti Kebangsaan Malaysia,Department of Applied Physics, Faculty of Science and Technology
[3] TUM (Technical University of Munich) Department of Informatics,School of Biological Sciences
[4] Bioinformatics & Computational Biology,Artificial Intelligence Institute
[5] Seoul National University,European Molecular Biology Laboratory
[6] Seoul National University,undefined
[7] European Bioinformatics Institute,undefined
[8] Institute for Advanced Study (TUM-IAS),undefined
[9] TUM School of Life Sciences Weihenstephan (WZW),undefined
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Communications Biology | / 6卷
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摘要
Deep-learning (DL) methods like DeepMind’s AlphaFold2 (AF2) have led to substantial improvements in protein structure prediction. We analyse confident AF2 models from 21 model organisms using a new classification protocol (CATH-Assign) which exploits novel DL methods for structural comparison and classification. Of ~370,000 confident models, 92% can be assigned to 3253 superfamilies in our CATH domain superfamily classification. The remaining cluster into 2367 putative novel superfamilies. Detailed manual analysis on 618 of these, having at least one human relative, reveal extremely remote homologies and further unusual features. Only 25 novel superfamilies could be confirmed. Although most models map to existing superfamilies, AF2 domains expand CATH by 67% and increases the number of unique ‘global’ folds by 36% and will provide valuable insights on structure function relationships. CATH-Assign will harness the huge expansion in structural data provided by DeepMind to rationalise evolutionary changes driving functional divergence.
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