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Improved protein surface comparison and application to low-resolution protein structure data

机译:改进的蛋白质表面比较和在低分辨率蛋白质结构数据中的应用

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摘要

Background: Recent advancements of experimental techniques for determining protein tertiary structures raise significant challenges for protein bioinformatics. With the number of known structures of unknown function expanding at a rapid pace, an urgent task is to provide reliable clues to their biological function on a large scale. Conventional approaches for structure comparison are not suitable for a real-time database search due to their slow speed. Moreover, a new challenge has arisen from recent techniques such as electron microscopy (EM), which provide low-resolution structure data. Previously, we have introduced a method for protein surface shape representation using the 3D Zernike descriptors (3DZDs). The 3DZD enables fast structure database searches, taking advantage of its rotation invariance and compact representation. The search results of protein surface represented with the 3DZD has showngood agreement with the existing structure classifications, but some discrepancies were also observed. Results: The three new surface representations of backbone atoms, originally devised all-atom-surface representation, and the combination of all-atom surface with the backbone representation are examined. All representations are encoded with the 3DZD. Also, we have investigated the applicability of the 3DZD for searching protein EM density maps of varying resolutions. The surface representations are evaluated on structure retrieval using two existing classifications, SCOP and the CE-based classification. Conclusions: Overall, the 3DZDs representing backbone atoms show better retrieval performance than the original all-atom surface representation. The performance further improved when the two representations are combined. Moreover, we observed that the 3DZD is also powerful in comparing low-resolution structures obtained by electron microscopy.
机译:背景:用于确定蛋白质三级结构的实验技术的最新进展对蛋白质生物信息学提出了重大挑战。随着功能未知的已知结构的数量迅速增加,迫切的任务是为它们的生物学功能提供可靠的线索。传统的结构比较方法由于速度较慢,因此不适用于实时数据库搜索。而且,诸如电子显微镜(EM)的最新技术已经提出了新的挑战,该技术提供了低分辨率的结构数据。以前,我们已经介绍了使用3D Zernike描述子(3DZDs)进行蛋白质表面形状表示的方法。 3DZD利用其旋转不变性和紧凑的表示形式,实现了快速结构数据库搜索。 3DZD表示的蛋白质表面搜索结果与现有的结构分类具有很好的一致性,但也观察到一些差异。结果:研究了最初设计为全原子-表面表示的三个新的骨架原子表面表示,并检查了全原子表面与骨架表示的组合。所有表示均使用3DZD编码。另外,我们还研究了3DZD在搜索不同分辨率的蛋白质EM密度图时的适用性。在使用两个现有分类(SCOP和基于CE的分类)进行结构检索时,将评估表面表示形式。结论:总的来说,代表主链原子的3DZD显示出比原始的全原子表面表示更好的检索性能。将两种表示形式组合时,性能进一步提高。此外,我们观察到3DZD在比较通过电子显微镜获得的低分辨率结构方面也很强大。

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  • 会议地点 Hangzhou(CN);Hangzhou(CN)
  • 作者

    Lee Sael; Daisuke Kihara;

  • 作者单位

    Department of Computer Science, Purdue University, 305 North University Street, West Lafayette, IN, 47907, USA;

    Department of Biological Sciences, Purdue University, Hockmyer Hall of Structural Biology, 249 S. Martin Jischke Drive, West Lafayette, IN, 47907, USA Department of Computer Science, Purdue University, 305 North University Street, West Lafayette, IN, 47907, USA Markey Center for Structural Biology, Purdue University, Hockmyer Hall of Structural Biology, 249 S. Martin Jischke Drive, West Lafayette, IN, 47907, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 基因理论;基因理论;
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