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MSV3d: database of human MisSense variants mapped to 3D protein structure

The elucidation of the complex relationships linking genotypic and phenotypic variations to protein structure is a major challenge in the post-genomic era. We present MSV3d (Database of human MisSense Variants mapped to 3D protein structure), a new database that contains detailed annotation of misse...

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Autores principales: Luu, Tien-Dao, Rusu, Alin-Mihai, Walter, Vincent, Ripp, Raymond, Moulinier, Luc, Muller, Jean, Toursel, Thierry, Thompson, Julie D., Poch, Olivier, Nguyen, Hoan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317913/
https://www.ncbi.nlm.nih.gov/pubmed/22491796
http://dx.doi.org/10.1093/database/bas018
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author Luu, Tien-Dao
Rusu, Alin-Mihai
Walter, Vincent
Ripp, Raymond
Moulinier, Luc
Muller, Jean
Toursel, Thierry
Thompson, Julie D.
Poch, Olivier
Nguyen, Hoan
author_facet Luu, Tien-Dao
Rusu, Alin-Mihai
Walter, Vincent
Ripp, Raymond
Moulinier, Luc
Muller, Jean
Toursel, Thierry
Thompson, Julie D.
Poch, Olivier
Nguyen, Hoan
author_sort Luu, Tien-Dao
collection PubMed
description The elucidation of the complex relationships linking genotypic and phenotypic variations to protein structure is a major challenge in the post-genomic era. We present MSV3d (Database of human MisSense Variants mapped to 3D protein structure), a new database that contains detailed annotation of missense variants of all human proteins (20 199 proteins). The multi-level characterization includes details of the physico-chemical changes induced by amino acid modification, as well as information related to the conservation of the mutated residue and its position relative to functional features in the available or predicted 3D model. Major releases of the database are automatically generated and updated regularly in line with the dbSNP (database of Single Nucleotide Polymorphism) and SwissVar releases, by exploiting the extensive Décrypthon computational grid resources. The database (http://decrypthon.igbmc.fr/msv3d) is easily accessible through a simple web interface coupled to a powerful query engine and a standard web service. The content is completely or partially downloadable in XML or flat file formats. Database URL: http://decrypthon.igbmc.fr/msv3d
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spelling pubmed-33179132012-04-04 MSV3d: database of human MisSense variants mapped to 3D protein structure Luu, Tien-Dao Rusu, Alin-Mihai Walter, Vincent Ripp, Raymond Moulinier, Luc Muller, Jean Toursel, Thierry Thompson, Julie D. Poch, Olivier Nguyen, Hoan Database (Oxford) Database Tool The elucidation of the complex relationships linking genotypic and phenotypic variations to protein structure is a major challenge in the post-genomic era. We present MSV3d (Database of human MisSense Variants mapped to 3D protein structure), a new database that contains detailed annotation of missense variants of all human proteins (20 199 proteins). The multi-level characterization includes details of the physico-chemical changes induced by amino acid modification, as well as information related to the conservation of the mutated residue and its position relative to functional features in the available or predicted 3D model. Major releases of the database are automatically generated and updated regularly in line with the dbSNP (database of Single Nucleotide Polymorphism) and SwissVar releases, by exploiting the extensive Décrypthon computational grid resources. The database (http://decrypthon.igbmc.fr/msv3d) is easily accessible through a simple web interface coupled to a powerful query engine and a standard web service. The content is completely or partially downloadable in XML or flat file formats. Database URL: http://decrypthon.igbmc.fr/msv3d Oxford University Press 2012-04-03 /pmc/articles/PMC3317913/ /pubmed/22491796 http://dx.doi.org/10.1093/database/bas018 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 Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Database Tool
Luu, Tien-Dao
Rusu, Alin-Mihai
Walter, Vincent
Ripp, Raymond
Moulinier, Luc
Muller, Jean
Toursel, Thierry
Thompson, Julie D.
Poch, Olivier
Nguyen, Hoan
MSV3d: database of human MisSense variants mapped to 3D protein structure
title MSV3d: database of human MisSense variants mapped to 3D protein structure
title_full MSV3d: database of human MisSense variants mapped to 3D protein structure
title_fullStr MSV3d: database of human MisSense variants mapped to 3D protein structure
title_full_unstemmed MSV3d: database of human MisSense variants mapped to 3D protein structure
title_short MSV3d: database of human MisSense variants mapped to 3D protein structure
title_sort msv3d: database of human missense variants mapped to 3d protein structure
topic Database Tool
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317913/
https://www.ncbi.nlm.nih.gov/pubmed/22491796
http://dx.doi.org/10.1093/database/bas018
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