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The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes
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) pu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964973/ https://www.ncbi.nlm.nih.gov/pubmed/24319146 http://dx.doi.org/10.1093/nar/gkt1243 |
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author | Furnham, Nicholas Holliday, Gemma L. de Beer, Tjaart A. P. Jacobsen, Julius O. B. Pearson, William R. Thornton, Janet M. |
author_facet | Furnham, Nicholas Holliday, Gemma L. de Beer, Tjaart A. P. Jacobsen, Julius O. B. Pearson, William R. Thornton, Janet M. |
author_sort | Furnham, Nicholas |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3964973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39649732014-03-25 The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes Furnham, Nicholas Holliday, Gemma L. de Beer, Tjaart A. P. Jacobsen, Julius O. B. Pearson, William R. Thornton, Janet M. Nucleic Acids Res III. Metabolic and signalling pathways, enzymes 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. Oxford University Press 2014-01-01 2013-12-05 /pmc/articles/PMC3964973/ /pubmed/24319146 http://dx.doi.org/10.1093/nar/gkt1243 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | III. Metabolic and signalling pathways, enzymes Furnham, Nicholas Holliday, Gemma L. de Beer, Tjaart A. P. Jacobsen, Julius O. B. Pearson, William R. Thornton, Janet M. The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
title | The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
title_full | The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
title_fullStr | The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
title_full_unstemmed | The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
title_short | The Catalytic Site Atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
title_sort | catalytic site atlas 2.0: cataloging catalytic sites and residues identified in enzymes |
topic | III. Metabolic and signalling pathways, enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964973/ https://www.ncbi.nlm.nih.gov/pubmed/24319146 http://dx.doi.org/10.1093/nar/gkt1243 |
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