Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

CSA

General information

URL: http://www.ebi.ac.uk/thornton-srv/databases/CSA/
Full name: Catalytic Site Atlas
Description: The Catalytic Site Atlas (CSA) is a database documenting enzyme active sites and catalytic residues in enzymes of 3D structure.
Year founded: 2004
Last update: NA
Version: v2.0
Accessibility:
Accessible
Country/Region: United Kingdom

Classification & Tag

Data type:
Data object:
NA
Database category:
Major species:
NA
Keywords:

Contact information

University/Institution: European Bioinformatics Institute
Address: Hinxton,Cambridge CB10 1SD,UK
City: Cambridge
Province/State: Cambridgeshire
Country/Region: United Kingdom
Contact name (PI/Team): Janet Thornton
Contact email (PI/Helpdesk): thornton@ebi.ac.uk

Publications

24319146
The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes. [PMID: 24319146]
Furnham N, Holliday GL, de Beer TA, Jacobsen JO, Pearson WR, Thornton JM.

Understanding which are the catalytic residues in an enzyme and what function they perform is crucial to many biology studies, particularly those leading to new therapeutics and enzyme design. The original version of the Catalytic Site Atlas (CSA) (http://www.ebi.ac.uk/thornton-srv/databases/CSA) published in 2004, which catalogs the residues involved in enzyme catalysis in experimentally determined protein structures, had only 177 curated entries and employed a simplistic approach to expanding these annotations to homologous enzyme structures. Here we present a new version of the CSA (CSA 2.0), which greatly expands the number of both curated (968) and automatically annotated catalytic sites in enzyme structures, utilizing a new method for annotation transfer. The curated entries are used, along with the variation in residue type from the sequence comparison, to generate 3D templates of the catalytic sites, which in turn can be used to find catalytic sites in new structures. To ease the transfer of CSA annotations to other resources a new ontology has been developed: the Enzyme Mechanism Ontology, which has permitted the transfer of annotations to Mechanism, Annotation and Classification in Enzymes (MACiE) and UniProt Knowledge Base (UniProtKB) resources. The CSA database schema has been re-designed and both the CSA data and search capabilities are presented in a new modern web interface.

Nucleic Acids Res. 2014:42(Database issue) | 134 Citations (from Europe PMC, 2025-12-13)
14681376
The Catalytic Site Atlas: a resource of catalytic sites and residues identified in enzymes using structural data. [PMID: 14681376]
Porter CT, Bartlett GJ, Thornton JM.

The Catalytic Site Atlas (CSA) provides catalytic residue annotation for enzymes in the Protein Data Bank. It is available online at http://www.ebi.ac.uk/thornton-srv/databases/CSA. The database consists of two types of annotated site: an original hand-annotated set containing information extracted from the primary literature, using defined criteria to assign catalytic residues, and an additional homologous set, containing annotations inferred by PSI-BLAST and sequence alignment to one of the original set. The CSA can be queried via Swiss-Prot identifier and EC number, as well as by PDB code. CSA Version 1.0 contains 177 original hand- annotated entries and 2608 homologous entries, and covers approximately 30% of all EC numbers found in PDB. The CSA will be updated on a monthly basis to include homologous sites found in new PDBs, and new hand-annotated enzymes as and when their annotation is completed.

Nucleic Acids Res. 2004:32(Database issue) | 434 Citations (from Europe PMC, 2025-12-13)

Ranking

All databases:
608/6895 (91.197%)
Structure:
66/967 (93.278%)
Gene genome and annotation:
219/2021 (89.213%)
608
Total Rank
551
Citations
26.238
z-index

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Record metadata

Created on: 2015-06-20
Curated by:
Alex Bateman [2022-06-20]
Lina Ma [2019-07-29]
Lina Ma [2018-06-05]
Mengwei Li [2016-03-31]
Mengwei Li [2016-02-21]
Mengwei Li [2015-12-06]
Mengwei Li [2015-06-29]
Mengwei Li [2015-06-27]