Laboratoire de Bioinformatique et Génomique Intégratives, Institut de Génétique et de Biologie Moléculaire et Cellulaire (UMR7104), 67404 Illkirch.
Database (Oxford). 2012 Apr 3;2012:bas018. doi: 10.1093/database/bas018. Print 2012.
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.
阐明基因型和表型变异与蛋白质结构之间的复杂关系是后基因组时代的主要挑战。我们介绍了 MSV3d(映射到 3D 蛋白质结构的人类误义变异数据库),这是一个新的数据库,其中包含所有人类蛋白质(20199 个蛋白质)的误义变异的详细注释。多层次的特征描述包括氨基酸修饰引起的理化变化的细节,以及与突变残基的保守性及其在可用或预测的 3D 模型中相对于功能特征的位置相关的信息。主要版本的数据库是通过利用广泛的 Décrypthon 计算网格资源,根据 dbSNP(单核苷酸多态性数据库)和 SwissVar 版本自动生成和定期更新的。数据库(http://decrypthon.igbmc.fr/msv3d)通过简单的 Web 界面与强大的查询引擎和标准 Web 服务相结合,易于访问。内容可以以 XML 或平面文件格式完全或部分下载。数据库 URL:http://decrypthon.igbmc.fr/msv3d。