Abstract

CATH version 3.3 (class, architecture, topology, homology) contains 128,688 domains, 2386 homologous superfamilies and 1233 fold groups, and reflects a major focus on classifying structural genomics (SG) structures and transmembrane proteins, both of which are likely to add structural novelty to the database and therefore increase the coverage of protein fold space within CATH. For CATH version 3.4 we have significantly improved the presentation of sequence information and associated functional information for CATH superfamilies. The CATH superfamily pages now reflect both the functional and structural diversity within the superfamily and include structural alignments of close and distant relatives within the superfamily, annotated with functional information and details of conserved residues. A significantly more efficient search function for CATH has been established by implementing the search server Solr (http://lucene.apache.org/solr/). The CATH v3.4 webpages have been built using the Catalyst web framework.

Keywords

BiologyStructure functionFunction (biology)Protein structureComputational biologyCath labEvolutionary biologyPhysicsInternal medicineBiochemistry

MeSH Terms

DatabasesProteinPhylogenyProtein FoldingProtein StructureTertiaryProteins

Affiliated Institutions

Related Publications

Publication Info

Year
2010
Type
article
Volume
39
Issue
Database
Pages
D420-D426
Citations
137
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

137
OpenAlex
20
Influential
117
CrossRef

Cite This

Alison Cuff, I. Sillitoe, Ted G. Lewis et al. (2010). Extending CATH: increasing coverage of the protein structure universe and linking structure with function. Nucleic Acids Research , 39 (Database) , D420-D426. https://doi.org/10.1093/nar/gkq1001

Identifiers

DOI
10.1093/nar/gkq1001
PMID
21097779
PMCID
PMC3013636

Data Quality

Data completeness: 90%