首页> 外文会议>International Workshop on Algorithms in Bioinformatics(WABI 2004); 20040917-21; Bergen(NO) >Protein-Protein Interfaces: Recognition of Similar Spatial and Chemical Organizations
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Protein-Protein Interfaces: Recognition of Similar Spatial and Chemical Organizations

机译:蛋白质-蛋白质界面:相似的空间和化学组织的识别

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Protein-protein interfaces, which are regions of interaction between two protein molecules, contain information about patterns of interacting functional groups. Recognition of such patterns is useful both for prediction of binding partners and for the development of drugs that can interfere with the formation of the protein-protein complex. We present a novel method, Interface-to-Interface (I2I)-SiteEngine, for structural alignment between two protein-protein interfaces. The method simultaneously aligns two pairs of binding sites that constitute an interface. The method is based on recognition of similarity of physico-chemical properties and shapes. It assumes no similarity of sequences or folds of the proteins that comprise the interfaces. Similarities between interfaces recognized by I2I-SiteEngine provide an insight into the interactions that are essential for the formation of the complex and can be related to its function. Its high efficiency makes it suitable for large scale database searches and classifications.
机译:蛋白质-蛋白质界面是两个蛋白质分子之间相互作用的区域,包含有关相互作用的官能团模式的信息。这种模式的识别对于预测结合伴侣和开发可干扰蛋白质-蛋白质复合物形成的药物都是有用的。我们提出了一种新颖的方法,接口到接口(I2I)-SiteEngine,用于两个蛋白质-蛋白质界面之间的结构比对。该方法同时比对构成界面的两对结合位点。该方法基于理化性质和形状相似性的识别。它假定组成界面的蛋白质的序列或折叠没有相似性。 I2I-SiteEngine识别的接口之间的相似性提供了对相互作用的深入了解,这些相互作用对于形成复合物至关重要,并且可以与其功能相关。它的高效率使其适用于大规模数据库搜索和分类。

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