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MolProbity:蛋白质和核酸的全原子接触与结构验证

MolProbity: all-atom contacts and structure validation for proteins and nucleic acids.

作者信息

Davis Ian W, Leaver-Fay Andrew, Chen Vincent B, Block Jeremy N, Kapral Gary J, Wang Xueyi, Murray Laura W, Arendall W Bryan, Snoeyink Jack, Richardson Jane S, Richardson David C

机构信息

Department of Biochemistry, Duke University, Durham, NC, USA.

出版信息

Nucleic Acids Res. 2007 Jul;35(Web Server issue):W375-83. doi: 10.1093/nar/gkm216. Epub 2007 Apr 22.

Abstract

MolProbity is a general-purpose web server offering quality validation for 3D structures of proteins, nucleic acids and complexes. It provides detailed all-atom contact analysis of any steric problems within the molecules as well as updated dihedral-angle diagnostics, and it can calculate and display the H-bond and van der Waals contacts in the interfaces between components. An integral step in the process is the addition and full optimization of all hydrogen atoms, both polar and nonpolar. New analysis functions have been added for RNA, for interfaces, and for NMR ensembles. Additionally, both the web site and major component programs have been rewritten to improve speed, convenience, clarity and integration with other resources. MolProbity results are reported in multiple forms: as overall numeric scores, as lists or charts of local problems, as downloadable PDB and graphics files, and most notably as informative, manipulable 3D kinemage graphics shown online in the KiNG viewer. This service is available free to all users at http://molprobity.biochem.duke.edu.

摘要

MolProbity是一个通用的网络服务器,可为蛋白质、核酸及复合物的三维结构提供质量验证。它能对分子内的任何空间问题进行详细的全原子接触分析,并提供更新的二面角诊断,还能计算并显示各组分间界面处的氢键和范德华接触。该过程中的一个重要步骤是添加并全面优化所有极性和非极性氢原子。现已为RNA、界面及核磁共振系综添加了新的分析功能。此外,网站和主要组件程序均已重写,以提高速度、便利性、清晰度,并增强与其他资源的整合。MolProbity的结果以多种形式呈现:作为总体数值分数、作为局部问题的列表或图表、作为可下载的PDB和图形文件,最值得注意的是作为在KiNG查看器中在线显示的信息丰富、可操作的三维动画图形。所有用户均可免费在http://molprobity.biochem.duke.edu使用此服务。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80aa/1933162/2ebc7fd82cf7/gkm216f1.jpg

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