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Redundant interactions in protein rigid cluster analysis

机译:蛋白质刚性聚类分析中的冗余相互作用

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Folded proteins are held together mainly by weak noncovalent interactions. We propose a method for classifying which of these interactions are critical to maintaining the protein's 3D shape, using information about their redundancy within the rigid clusters of atoms. We have developed KINARI-Web, a server performing rigidity analysis of proteins. It implements pebble game analysis to determine rigid clusters and flexibility information. The method presented here is provided as an additional module. We classify each of the noncovalent interactions as either redundant or critical. An interaction is critical if removing it would cause the rigid cluster to break apart and become flexible, otherwise an interaction is redundant. In addition, we propose a new method for assigning scores to the rigid clusters based on the number of redundant and critical interactions in the cluster. We present data on the redundancy of the rigid clusters of cytochrome c, barnase, and a dataset of kinases.
机译:折叠的蛋白质主要通过弱的非共价相互作用保持在一起。我们提出了一种用于将这些相互作用中的哪一个对维持蛋白质的3D形状至关重要的方法,利用关于刚性原子内的刚性簇内的冗余的信息。我们开发了Kinari-Web,一种表现蛋白质刚性分析的服务器。它实现了Pebble游戏分析,以确定刚性集群和灵活性信息。这里呈现的方法作为附加模块提供。我们将每个非共价交互分类为冗余或关键。如果删除它会导致刚性集群分开并变得灵活,则交互是至关重要的,否则互动是冗余的。此外,我们提出了一种新方法,用于基于集群中的冗余和临界交互的数量为刚性群集分配分数。我们呈现关于细胞色素C,Barnase和激酶数据集的刚性簇的冗余数据。

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