Peterson Lenna X, Kim Hyungrae, Esquivel-Rodriguez Juan, Roy Amitava, Han Xusi, Shin Woong-Hee, Zhang Jian, Terashi Genki, Lee Matt, Kihara Daisuke
Department of Biological Sciences, Purdue University, West Lafayette, Indiana.
Department of Computer Science, Purdue University, West Lafayette, Indiana.
Proteins. 2017 Mar;85(3):513-527. doi: 10.1002/prot.25165. Epub 2016 Oct 14.
We report the performance of protein-protein docking predictions by our group for recent rounds of the Critical Assessment of Prediction of Interactions (CAPRI), a community-wide assessment of state-of-the-art docking methods. Our prediction procedure uses a protein-protein docking program named LZerD developed in our group. LZerD represents a protein surface with 3D Zernike descriptors (3DZD), which are based on a mathematical series expansion of a 3D function. The appropriate soft representation of protein surface with 3DZD makes the method more tolerant to conformational change of proteins upon docking, which adds an advantage for unbound docking. Docking was guided by interface residue prediction performed with BindML and cons-PPISP as well as literature information when available. The generated docking models were ranked by a combination of scoring functions, including PRESCO, which evaluates the native-likeness of residues' spatial environments in structure models. First, we discuss the overall performance of our group in the CAPRI prediction rounds and investigate the reasons for unsuccessful cases. Then, we examine the performance of several knowledge-based scoring functions and their combinations for ranking docking models. It was found that the quality of a pool of docking models generated by LZerD, that is whether or not the pool includes near-native models, can be predicted by the correlation of multiple scores. Although the current analysis used docking models generated by LZerD, findings on scoring functions are expected to be universally applicable to other docking methods. Proteins 2017; 85:513-527. © 2016 Wiley Periodicals, Inc.
我们报告了我们团队针对最近几轮蛋白质相互作用预测关键评估(CAPRI)所做的蛋白质-蛋白质对接预测的表现,CAPRI是一项对最先进对接方法的全领域评估。我们的预测程序使用了我们团队开发的名为LZerD的蛋白质-蛋白质对接程序。LZerD用基于三维函数数学级数展开的三维泽尼克描述符(3DZD)来表示蛋白质表面。用3DZD对蛋白质表面进行适当的软表示,使得该方法在对接时对蛋白质构象变化更具耐受性,这为未结合对接增添了优势。对接由使用BindML和cons-PPISP进行的界面残基预测以及可用的文献信息来引导。生成的对接模型通过包括PRESCO在内的多种评分函数的组合进行排名,PRESCO评估结构模型中残基空间环境的天然相似性。首先,我们讨论我们团队在CAPRI预测轮次中的整体表现,并调查未成功案例的原因。然后,我们检查几种基于知识的评分函数及其组合对对接模型进行排名的表现。发现通过多个分数的相关性可以预测由LZerD生成的一组对接模型的质量,即该组模型是否包含近天然模型。尽管当前分析使用的是由LZerD生成的对接模型,但关于评分函数的发现预计将普遍适用于其他对接方法。《蛋白质》2017年;85:513 - 527。©2016威利期刊公司。