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IUPHAR-DB: updated database content and new features

The International Union of Basic and Clinical Pharmacology (IUPHAR) database, IUPHAR-DB (http://www.iuphar-db.org) is an open access, online database providing detailed, expert-driven annotation of the primary literature on human and rodent receptors and other drug targets, together with the substan...

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Autores principales: Sharman, Joanna L., Benson, Helen E., Pawson, Adam J., Lukito, Veny, Mpamhanga, Chidochangu P., Bombail, Vincent, Davenport, Anthony P., Peters, John A., Spedding, Michael, Harmar, Anthony J., NC-IUPHAR
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531077/
https://www.ncbi.nlm.nih.gov/pubmed/23087376
http://dx.doi.org/10.1093/nar/gks960
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author Sharman, Joanna L.
Benson, Helen E.
Pawson, Adam J.
Lukito, Veny
Mpamhanga, Chidochangu P.
Bombail, Vincent
Davenport, Anthony P.
Peters, John A.
Spedding, Michael
Harmar, Anthony J.
NC-IUPHAR,
author_facet Sharman, Joanna L.
Benson, Helen E.
Pawson, Adam J.
Lukito, Veny
Mpamhanga, Chidochangu P.
Bombail, Vincent
Davenport, Anthony P.
Peters, John A.
Spedding, Michael
Harmar, Anthony J.
NC-IUPHAR,
author_sort Sharman, Joanna L.
collection PubMed
description The International Union of Basic and Clinical Pharmacology (IUPHAR) database, IUPHAR-DB (http://www.iuphar-db.org) is an open access, online database providing detailed, expert-driven annotation of the primary literature on human and rodent receptors and other drug targets, together with the substances that act on them. The present release includes information on the products of 646 genes from four major protein classes (G protein-coupled receptors, nuclear hormone receptors, voltage- and ligand-gated ion channels) and ∼3180 bioactive molecules (endogenous ligands, licensed drugs and key pharmacological tools) that interact with them. We have described previously the classification and curation of data for small molecule ligands in the database; in this update we have annotated 366 endogenous peptide ligands with their amino acid sequences, post-translational modifications, links to precursor genes, species differences and relationships with other molecules in the database (e.g. those derived from the same precursor). We have also matched targets with their endogenous ligands (peptides and small molecules), with particular attention paid to identifying bioactive peptide ligands generated by post-translational modification of precursor proteins. Other improvements to the database include enhanced information on the clinical relevance of targets and ligands in the database, more extensive links to other databases and a pilot project for the curation of enzymes as drug targets.
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spelling pubmed-35310772013-03-07 IUPHAR-DB: updated database content and new features Sharman, Joanna L. Benson, Helen E. Pawson, Adam J. Lukito, Veny Mpamhanga, Chidochangu P. Bombail, Vincent Davenport, Anthony P. Peters, John A. Spedding, Michael Harmar, Anthony J. NC-IUPHAR, Nucleic Acids Res Articles The International Union of Basic and Clinical Pharmacology (IUPHAR) database, IUPHAR-DB (http://www.iuphar-db.org) is an open access, online database providing detailed, expert-driven annotation of the primary literature on human and rodent receptors and other drug targets, together with the substances that act on them. The present release includes information on the products of 646 genes from four major protein classes (G protein-coupled receptors, nuclear hormone receptors, voltage- and ligand-gated ion channels) and ∼3180 bioactive molecules (endogenous ligands, licensed drugs and key pharmacological tools) that interact with them. We have described previously the classification and curation of data for small molecule ligands in the database; in this update we have annotated 366 endogenous peptide ligands with their amino acid sequences, post-translational modifications, links to precursor genes, species differences and relationships with other molecules in the database (e.g. those derived from the same precursor). We have also matched targets with their endogenous ligands (peptides and small molecules), with particular attention paid to identifying bioactive peptide ligands generated by post-translational modification of precursor proteins. Other improvements to the database include enhanced information on the clinical relevance of targets and ligands in the database, more extensive links to other databases and a pilot project for the curation of enzymes as drug targets. Oxford University Press 2013-01 2012-10-18 /pmc/articles/PMC3531077/ /pubmed/23087376 http://dx.doi.org/10.1093/nar/gks960 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/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 Articles
Sharman, Joanna L.
Benson, Helen E.
Pawson, Adam J.
Lukito, Veny
Mpamhanga, Chidochangu P.
Bombail, Vincent
Davenport, Anthony P.
Peters, John A.
Spedding, Michael
Harmar, Anthony J.
NC-IUPHAR,
IUPHAR-DB: updated database content and new features
title IUPHAR-DB: updated database content and new features
title_full IUPHAR-DB: updated database content and new features
title_fullStr IUPHAR-DB: updated database content and new features
title_full_unstemmed IUPHAR-DB: updated database content and new features
title_short IUPHAR-DB: updated database content and new features
title_sort iuphar-db: updated database content and new features
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531077/
https://www.ncbi.nlm.nih.gov/pubmed/23087376
http://dx.doi.org/10.1093/nar/gks960
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