CATH: increased structural coverage of functional space.

Ian Sillitoe, Nicola Bordin, Natalie Dawson,Vaishali P Waman,Paul Ashford, Harry M Scholes, Camilla S M Pang, Laurel Woodridge,Clemens Rauer, Neeladri Sen,Mahnaz Abbasian, Sean Le Cornu, Su Datt Lam,Karel Berka, Ivana Hutařová Varekova,Radka Svobodova, Jon Lees,Christine A Orengo

Nucleic acids research(2021)

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摘要
CATH (https://www.cathdb.info) identifies domains in protein structures from wwPDB and classifies these into evolutionary superfamilies, thereby providing structural and functional annotations. There are two levels: CATH-B, a daily snapshot of the latest domain structures and superfamily assignments, and CATH+, with additional derived data, such as predicted sequence domains, and functionally coherent sequence subsets (Functional Families or FunFams). The latest CATH+ release, version 4.3, significantly increases coverage of structural and sequence data, with an addition of 65,351 fully-classified domains structures (+15%), providing 500 238 structural domains, and 151 million predicted sequence domains (+59%) assigned to 5481 superfamilies. The FunFam generation pipeline has been re-engineered to cope with the increased influx of data. Three times more sequences are captured in FunFams, with a concomitant increase in functional purity, information content and structural coverage. FunFam expansion increases the structural annotations provided for experimental GO terms (+59%). We also present CATH-FunVar web-pages displaying variations in protein sequences and their proximity to known or predicted functional sites. We present two case studies (1) putative cancer drivers and (2) SARS-CoV-2 proteins. Finally, we have improved links to and from CATH including SCOP, InterPro, Aquaria and 2DProt.
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