Expediting protein structural analysis with an efficient kernel density estimation algorithm

Yen-Jen Oyang, Darby Tien-Hao Chang, Chien-Yu Chen, Shien-Ching Hwang
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引用次数: 2

Abstract

We describe a kernel density estimation based mechanism aimed at expediting protein structural analysis. We have been motivated by the observation that many protein structural analysis algorithms suffer high time complexity, while only the residues and atoms on the contour of a protein are essential for determining the functions of the protein and how it could interact with the other proteins. Accordingly, for some protein structural analysis problems, it is desirable to invoke a mechanism that can extract the residues and atoms on the contour of a protein in order to expedite the analysis process. The conventional approach to carry out this task is to invoke the /spl alpha/-hull algorithm from computer graphics, which features O(n/sup 2/) time complexity, where n is the number of residues or atoms in the protein. A kernel density estimation based expediting mechanism with an average time complexity of O(nlogn) is proposed. We also report the experiment conducted to evaluate the effects of applying the proposed expediting mechanism to a real protein structural analysis problem. Experimental results reveal that a speedup of 4.8 to 10.3 times can be achieved with minimum impact on the analysis accuracy.
用高效核密度估计算法加速蛋白质结构分析
我们描述了一种基于核密度估计的机制,旨在加快蛋白质结构分析。我们的动机是观察到许多蛋白质结构分析算法具有很高的时间复杂度,而只有蛋白质轮廓上的残基和原子对于确定蛋白质的功能以及它如何与其他蛋白质相互作用是必不可少的。因此,对于某些蛋白质结构分析问题,需要调用一种机制来提取蛋白质轮廓上的残基和原子,以加快分析过程。执行此任务的传统方法是调用计算机图形学中的/spl alpha/-hull算法,该算法具有O(n/sup 2/)时间复杂度,其中n是蛋白质中残基或原子的数量。提出了一种平均时间复杂度为0 (nlogn)的基于核密度估计的加速机制。我们还报道了将所提出的加速机制应用于实际蛋白质结构分析问题的效果的实验。实验结果表明,在对分析精度影响最小的情况下,可以实现4.8 ~ 10.3倍的加速。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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