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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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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 |
format | Online Article Text |
id | pubmed-3317913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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