Protein Packing Quality Using Delaunay Complexes

R. Fonseca, P. Winter, K. Karplus
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引用次数: 1

Abstract

A new method for estimating the packing quality of protein structures is presented. Atoms in high quality protein crystal structures are very uniformly distributed which is difficult to reproduce using structure prediction methods. Packing quality measures can therefore be used to assess structures of low quality and even to refine them. Previous methods mainly use the Voronoi cells of atoms to assess packing quality. The presented method uses only the lengths of edges in the Delaunay complex which is faster to compute since volumes of Voronoi cells are not evaluated explicitly. This is a novel application of the Delaunay complex that can improve the speed of packing quality computations. Doing so is an important step for, e.g., integrating packing measures into structure refinement methods. High- and low-resolution X-ray crystal structures were chosen to represent well- and poorly-packed structures respectively. Our results show that the developed method is correlated to the well-established RosettaHoles2 but three times faster.
Delaunay配合物的蛋白质包装质量研究
提出了一种估计蛋白质结构包装质量的新方法。高质量蛋白质晶体结构中的原子分布非常均匀,很难用结构预测方法再现。因此,包装质量措施可以用来评估低质量的结构,甚至改进它们。以往的方法主要是利用原子的Voronoi细胞来评价包装质量。所提出的方法仅使用Delaunay复合体中的边长度,由于Voronoi细胞的体积没有显式评估,因此计算速度更快。这是Delaunay复合体的一个新应用,可以提高包装质量计算的速度。这样做是一个重要的步骤,例如,将包装措施整合到结构改进方法中。选择高分辨率和低分辨率的x射线晶体结构分别代表良好和不良的结构。我们的结果表明,所开发的方法与已建立的RosettaHoles2相关,但速度快了三倍。
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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