| Literature DB >> 33237325 |
Ian Sillitoe1, Nicola Bordin1, Natalie Dawson1, Vaishali P Waman1, Paul Ashford1, Harry M Scholes1, Camilla S M Pang1, Laurel Woodridge1, Clemens Rauer1, Neeladri Sen1, Mahnaz Abbasian1, Sean Le Cornu1, Su Datt Lam2, Karel Berka3, Ivana Hutařová Varekova4, Radka Svobodova5, Jon Lees6, Christine A Orengo1.
Abstract
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.Entities:
Year: 2021 PMID: 33237325 DOI: 10.1093/nar/gkaa1079
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971