首页> 外文会议>International Conference on Genome Informatics >Improved protein surface comparison and application to low-resolution protein structure data
【24h】

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

机译:改善蛋白质表面比较和应用于低分辨率蛋白质结构数据

获取原文

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步促进了蛋白质生物信息学的显着挑战。随着以快速速度扩展的未知功能的已知结构的数量,紧急任务是在大规模上为其生物功能提供可靠的线索。由于它们的速度慢,结构比较的传统方法不适合实时数据库搜索。此外,从最近的诸如电子显微镜(EM)之类的技术中出现了新的挑战,其提供低分辨率结构数据。以前,我们已经使用3D Zernike描述符(3DZDS)介绍了一种蛋白质表面形状表示的方法。 3DZD启用快速结构数据库搜索,利用其旋转不变性和紧凑的表示。用3DZD表示的蛋白质表面的搜索结果与现有的结构分类表现出来,但也观察到一些差异。结果:检查骨架原子的三个新表面表示,最初设计了全原子表面表示,以及用骨干表示的全原子表面的组合。所有表示都与3DZD编码。此外,我们已经调查了3DZD用于搜索不同分辨率的蛋白质EM密度图的适用性。使用两个现有分类,SCOP和基于CE的分类来评估结构检索的表面表示。结论:总体而言,表示骨干原子的3DZDS显示出比原始全原子表面表示更好的检索性能。当两个表示组合时,性能进一步改善。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时也是强大的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号