This article provides an update of the latest data and developments within the CATH protein structure classification database (http://www.cathdb.info).
View Article and Find Full Text PDFGene3D (http://gene3d.biochem.ucl.
View Article and Find Full Text PDFThe latest version of the CATH-Gene3D protein structure classification database has recently been released (version 4.1, http://www.cathdb.
View Article and Find Full Text PDFCurr Protoc Bioinformatics
June 2015
The CATH database is a classification of protein structures found in the Protein Data Bank (PDB). Protein structures are chopped into individual units of structural domains, and these domains are grouped together into superfamilies if there is sufficient evidence that they have diverged from a common ancestor during the process of evolution. A sister resource, Gene3D, extends this information by scanning sequence profiles of these CATH domain superfamilies against many millions of known proteins to identify related sequences.
View Article and Find Full Text PDFNucleic Acids Res
January 2015
The latest version of the CATH-Gene3D protein structure classification database (4.0, http://www.cathdb.
View Article and Find Full Text PDFGenome3D (http://www.genome3d.eu) is a collaborative resource that provides predicted domain annotations and structural models for key sequences.
View Article and Find Full Text PDFGenome3D, available at http://www.genome3d.eu, is a new collaborative project that integrates UK-based structural resources to provide a unique perspective on sequence-structure-function relationships.
View Article and Find Full Text PDFCATH version 3.5 (Class, Architecture, Topology, Homology, available at http://www.cathdb.
View Article and Find Full Text PDFCATH 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.
View Article and Find Full Text PDFThis paper explores the structural continuum in CATH and the extent to which superfamilies adopt distinct folds. Although most superfamilies are structurally conserved, in some of the most highly populated superfamilies (4% of all superfamilies) there is considerable structural divergence. While relatives share a similar fold in the evolutionary conserved core, diverse elaborations to this core can result in significant differences in the global structures.
View Article and Find Full Text PDFThe latest version of CATH (class, architecture, topology, homology) (version 3.2), released in July 2008 (http://www.cathdb.
View Article and Find Full Text PDFBackground: Structural genomics initiatives were established with the aim of solving protein structures on a large-scale. For many initiatives, such as the Protein Structure Initiative (PSI), the primary aim of target selection is focussed towards structurally characterising protein families which, so far, lack a structural representative. It is therefore of considerable interest to gain insights into the number and distribution of these families, and what efforts may be required to achieve a comprehensive structural coverage across all protein families.
View Article and Find Full Text PDFWe report the latest release (version 3.0) of the CATH protein domain database (http://www.cathdb.
View Article and Find Full Text PDFThe CATH database of protein domain structures (http://www.biochem.ucl.
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