CavDetect:基于 DBSCAN 算法的蛋白质结构新空洞检测模型

Swati AdhikariThe University of Burdwan, Parthajit RoyThe University of Burdwan
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引用次数: 0

摘要

蛋白质结构上的空腔是由于蛋白质与一些小分子(称为配体)之间的相互作用而形成的。这些基本上是配体与蛋白质结合的位置。要在整个药物设计过程中取得成功,对这些位置的实际检测至关重要。本研究提出了一种基于 Voronoi Tessellation 的新型空穴检测模型,用于检测蛋白质结构上的空穴。由于蛋白质结构的原子空间密度大、体积大,而 DBSCAN 算法(基于密度的空间聚类算法)可以很好地处理这类数据,而且在该算法中不需要先验地了解数据中的聚类(空穴)数量,因此本研究建议用 DBSCAN 算法来实现所提出的算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CavDetect: A DBSCAN Algorithm based Novel Cavity Detection Model on Protein Structure
Cavities on the structures of proteins are formed due to interaction between proteins and some small molecules, known as ligands. These are basically the locations where ligands bind with proteins. Actual detection of such locations is all-important to succeed in the entire drug design process. This study proposes a Voronoi Tessellation based novel cavity detection model that is used to detect cavities on the structure of proteins. As the atom space of protein structure is dense and of large volumes and the DBSCAN (Density Based Spatial Clustering of Applications with Noise) algorithm can handle such type of data very well as well as it is not mandatory to have knowledge about the numbers of clusters (cavities) in data as priori in this algorithm, this study proposes to implement the proposed algorithm with the DBSCAN algorithm.
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