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LGICdb: a manually curated sequence database after the genomes

Ligand-gated ion channels form transmembrane ionic pores controlled by the binding of chemicals. The LGICdb aims to be a non-redundant, manually curated resource offering access to the large number of subunits composing extracellularly activated ligand-gated ion channels, such as nicotinic, ATP, GAB...

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Detalles Bibliográficos
Autores principales: Donizelli, Marco, Djite, Marie-Ange, Novère, Nicolas Le
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347466/
https://www.ncbi.nlm.nih.gov/pubmed/16381861
http://dx.doi.org/10.1093/nar/gkj104
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author Donizelli, Marco
Djite, Marie-Ange
Novère, Nicolas Le
author_facet Donizelli, Marco
Djite, Marie-Ange
Novère, Nicolas Le
author_sort Donizelli, Marco
collection PubMed
description Ligand-gated ion channels form transmembrane ionic pores controlled by the binding of chemicals. The LGICdb aims to be a non-redundant, manually curated resource offering access to the large number of subunits composing extracellularly activated ligand-gated ion channels, such as nicotinic, ATP, GABA and glutamate ionotropic receptors. Composed of more than 500 human curated entries, the XML native database has been relocated in 2004 to the EBI. Its facilities have been enhanced with a new search system, customized multiple sequence alignments and manipulation of protein structures (). Despite the vast improvement of general sequence resources, the LGICdb still provide sequences unavailable elsewhere.
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spelling pubmed-13474662006-01-25 LGICdb: a manually curated sequence database after the genomes Donizelli, Marco Djite, Marie-Ange Novère, Nicolas Le Nucleic Acids Res Article Ligand-gated ion channels form transmembrane ionic pores controlled by the binding of chemicals. The LGICdb aims to be a non-redundant, manually curated resource offering access to the large number of subunits composing extracellularly activated ligand-gated ion channels, such as nicotinic, ATP, GABA and glutamate ionotropic receptors. Composed of more than 500 human curated entries, the XML native database has been relocated in 2004 to the EBI. Its facilities have been enhanced with a new search system, customized multiple sequence alignments and manipulation of protein structures (). Despite the vast improvement of general sequence resources, the LGICdb still provide sequences unavailable elsewhere. Oxford University Press 2006-01-01 2005-12-28 /pmc/articles/PMC1347466/ /pubmed/16381861 http://dx.doi.org/10.1093/nar/gkj104 Text en © The Author 2006. Published by Oxford University Press. All rights reserved
spellingShingle Article
Donizelli, Marco
Djite, Marie-Ange
Novère, Nicolas Le
LGICdb: a manually curated sequence database after the genomes
title LGICdb: a manually curated sequence database after the genomes
title_full LGICdb: a manually curated sequence database after the genomes
title_fullStr LGICdb: a manually curated sequence database after the genomes
title_full_unstemmed LGICdb: a manually curated sequence database after the genomes
title_short LGICdb: a manually curated sequence database after the genomes
title_sort lgicdb: a manually curated sequence database after the genomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347466/
https://www.ncbi.nlm.nih.gov/pubmed/16381861
http://dx.doi.org/10.1093/nar/gkj104
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