Exploring structural diversity across the protein universe with The Encyclopedia of Domains

Andy M. Lau(University College London), Nicola Bordin(Institute of Structural and Molecular Biology), Shaun M. Kandathil(University College London), Ian Sillitoe(Institute of Structural and Molecular Biology), Vaishali Waman(Institute of Structural and Molecular Biology), Jude Wells(Institute of Structural and Molecular Biology), Christine Orengo(Institute of Structural and Molecular Biology), David T. Jones(Institute of Structural and Molecular Biology)
Science
October 31, 2024
Cited by 113Open Access
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Abstract

The AlphaFold Protein Structure Database (AFDB) contains more than 214 million predicted protein structures composed of domains, which are independently folding units found in multiple structural and functional contexts. Identifying domains can enable many functional and evolutionary analyses but has remained challenging because of the sheer scale of the data. Using deep learning methods, we have detected and classified every domain in the AFDB, producing The Encyclopedia of Domains. We detected nearly 365 million domains, over 100 million more than can be found by sequence methods, covering more than 1 million taxa. Reassuringly, 77% of the nonredundant domains are similar to known superfamilies, greatly expanding representation of their domain space. We uncovered more than 10,000 new structural interactions between superfamilies and thousands of new folds across the fold space continuum.


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