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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...

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Autores principales: Furnham, Nicholas, Holliday, Gemma L., de Beer, Tjaart A. P., Jacobsen, Julius O. B., Pearson, William R., Thornton, Janet M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
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.
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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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