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Phylogeny-independent detection of functional residues

机译:系统发育无关的功能残基检测

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Motivation: Current projects for the massive characterization of proteomes are generating protein sequences and structures with unknown function. The difficulty of experimentally determining functionally important sites calls for the development of computational methods. The first techniques, based on the search for fully conserved positions in multiple sequence alignments (MSAs), were followed by methods for locating family-dependent conserved positions. These rely on the functional classification implicit in the alignment for locating these positions related with functional specificity. The next obvious step, still scarcely explored, is to detect these positions using a functional classification different from the one implicit in the sequence relationships between the proteins. Here, we present two new methods for locating functional positions which can incorporate an arbitrary external functional classification which may or may not coincide with the one implicit in the MSA. The Xdet method is able to use a functional classification with an associated hierarchy or similarity between functions to locate positions related to that classification. The MCdet method uses multivariate statistical analysis to locate positions responsible for each one of the functions within a multifunctional family.
机译:动机:目前对蛋白质组进行大规模表征的项目正在产生功能未知的蛋白质序列和结构。通过实验确定功能上重要的位点的困难要求开发计算方法。最初的技术基于在多个序列比对(MSA)中寻找完全保守的位置,随后是定位家族依赖性保守位置的方法。这些依赖于比对中隐含的功能分类来定位与功能特异性有关的这些位置。仍然很少探索的下一个明显步骤是,使用不同于蛋白质之间序列关系中隐含的功能分类的功能分类来检测这些位置。在这里,我们介绍了两种定位功能位置的新方法,这些方法可以合并一个任意外部功能分类,该分类可能与或可能与MSA中隐含的一个不一致。 Xdet方法能够使用具有相关层次结构或功能之间相似性的功能分类来定位与该分类相关的位置。 MCdet方法使用多元统计分析来定位负责多功能族中每个功能的位置。

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