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Binding Site Extraction by Similar Subgraphs Mining from Protein Molecular Surfaces and Its Application to Protein Classification

机译:蛋白质分子表面相似子图的结合位点提取及其在蛋白质分类中的应用

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摘要

Most proteins express their functions by binding with other proteins or molecular compounds (ligands). Since the characteristics of the local portion involved in binding (binding site) often determine the function of the protein, clarifying the location of the binding site of the protein helps analyze the function of proteins. Binding sites that bind to similar ligands often have common surface structures (surface motifs). Extracting the surface motifs among several proteins with similar functions improves binding site prediction. We propose a method that predicts binding sites by extracting the surface motifs that are frequently observed in only a specific set of proteins that bind to the same ligand (group). Since most binding sites have concave structures (pockets), the pockets are compared and common structures are searched for to extract the surface motifs by applying similar graph mining to the pocket data, which are represented as graphs. Common binding sites across several groups can be predicted in such a way to integrate more than one group. We also proposed a method of protein classification, in which the surface motifs extracted using the above method are evaluated on the assumption that a protein belongs to each one of the groups.
机译:大多数蛋白质通过与其他蛋白质或分子化合物(配体)结合来表达其功能。由于参与结合的局部部分的特征(结合位点)通常决定蛋白质的功能,因此弄清蛋白质结合位点的位置有助于分析蛋白质的功能。与相似配体结合的结合位点通常具有共同的表面结构(表面基序)。从具有相似功能的几种蛋白质中提取表面基序可改善结合位点的预测。我们提出了一种方法,该方法通过提取仅在结合同一配体(组)的一组特定蛋白质中经常观察到的表面基序来预测结合位点。由于大多数绑定位点都具有凹结构(口袋),因此可以对口袋进行比较,并通过对口袋数据(以图表表示)进行类似的图形挖掘来搜索常见结构以提取表面图案。可以通过整合多个组的方式来预测多个组之间的公共结合位点。我们还提出了一种蛋白质分类的方法,其中在假定蛋白质属于每个组的前提下,对使用上述方法提取的表面基序进行了评估。

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