CATH database

The CATH Protein Structure Classification database is a free, publicly available online resource that provides information on the evolutionary relationships of protein domains. It was created in the mid-1990s by Professor Christine Orengo and colleagues including Janet Thornton and David Jones,[2] and continues to be developed by the Orengo group at University College London. CATH shares many broad features with the SCOP resource, however there are also many areas in which the detailed classification differs greatly.[3][4][5][6]

CATH
Content
DescriptionProtein Structure Classification
Contact
Research centerUniversity College London
LaboratoryInstitute of Structural and Molecular Biology
Primary citationDawson et al. (2016) [1]
Release date1997
Access
Websitecathdb.info
Download URLcathdb.info/download
Miscellaneous
Data release
frequency		CATH-B is released daily. Official releases are approximately annual.
Version4.1

Hierarchical organization

Experimentally-determined protein three-dimensional structures are obtained from the Protein Data Bank and split into their consecutive polypeptide chains, where applicable. Protein domains are identified within these chains using a mixture of automatic methods and manual curation.

The domains are then classified within the CATH structural hierarchy: at the Class (C) level, domains are assigned according to their secondary structure content, i.e. all alpha, all beta, a mixture of alpha and beta, or little secondary structure; at the Architecture (A) level, information on the secondary structure arrangement in three-dimensional space is used for assignment; at the Topology/fold (T) level, information on how the secondary structure elements are connected and arranged is used; assignments are made to the Homologous superfamily (H) level if there is good evidence that the domains are related by evolution [2] i.e. they are homologous.

The four main levels of the CATH hierarchy:
# Level Description
1Classthe overall secondary-structure content of the domain. (Equivalent to the SCOP Class)
2Architecturehigh structural similarity but no evidence of homology. (Equivalent to the 'fold' level in SCOP)
3Topology/folda large-scale grouping of topologies which share particular structural features
4Homologous superfamilyindicative of a demonstrable evolutionary relationship. (Equivalent to SCOP superfamily)

Additional sequence data for domains with no experimentally determined structures are provided by CATH's sister resource, Gene3D, which are used to populate the homologous superfamilies. Protein sequences from UniProtKB and Ensembl are scanned against CATH HMMs to predict domain sequence boundaries and make homologous superfamily assignments.

Releases

The CATH team aim to provide official releases of the CATH classification every 12 months. This release process is important because it allows for the provision of internal validation, extra annotations and analysis. However, it can mean that there is a time delay between new structures appearing in the PDB and the latest official CATH release,

In order to address this issue: CATH-B provides a limited amount of information to the very latest domain annotations (e.g. domain boundaries and superfamily classifications).

The latest release of CATH-Gene3D (v4.1) was released in July 2016 and consists of:

  • 308,999 structural protein domain entries [1]
  • 53,479,436 non-structural protein domain entries [1]
  • 2,737 homologous superfamily entries [1]
  • 92,882 functional family entries [1]

Open source software

CATH is an open source software project, with developers developing and maintaining a number of open source tools.[7] CATH maintains a todo list on GitHub to allow external users to create and keep track of issues relating to the CATH protein structure classification.

gollark: Yes. "Lyricly" is the alleged author of "Macron".
gollark: <@509849474647064576> contingency aleph-9
gollark: I don't know if they needed rethinking but TOO BAD.
gollark: Anyway, the current implementation (7.1) is Python/JS frontend, but this is kind of æ so I want to carcinize it, particularly since I rethought major aspects of the design.
gollark: That looks far too short to be CommonMark-compliant.

References
  1. Dawson, NL; Lewis, TE; Das, S; Lees, JG; Lee, D; Ashford, P; Orengo, CA; Sillitoe, I (28 November 2016). "CATH: an expanded resource to predict protein function through structure and sequence". Nucleic Acids Research. 45 (D1): D289–D295. doi:10.1093/nar/gkw1098. PMC 5210570. PMID 27899584.
  2. Orengo, CA; Michie, AD; Jones, S; Jones, DT; Swindells, MB; Thornton, JM (1997). "CATH – a hierarchic classification of protein domain structures". Structure. 5 (8): 1093–1109. doi:10.1016/S0969-2126(97)00260-8. ISSN 0969-2126. PMID 9309224.
  3. "CATH: Protein Structure Classification Database at UCL". Cathdb.info. Retrieved 9 March 2017.
  4. "CATH". Cathdb.info. Retrieved 9 March 2017.
  5. "CATH Database (@CATHDatabase)". Twitter. Retrieved 9 March 2017.
  6. Pearl, F. M. G. (2003). "The CATH database: an extended protein family resource for structural and functional genomics". Nucleic Acids Research. 31 (1): 452–455. doi:10.1093/nar/gkg062. ISSN 1362-4962. PMC 165509. PMID 12520050.
  7. "Tools". cathdb.info. Retrieved 18 December 2016.

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