Pierce Brian, Weng Zhiping
Bioinformatics Program, Department of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, USA.
Proteins. 2007 Jun 1;67(4):1078-86. doi: 10.1002/prot.21373.
Protein-protein docking requires fast and effective methods to quickly discriminate correct from incorrect predictions generated by initial-stage docking. We have developed and tested a scoring function that utilizes detailed electrostatics, van der Waals, and desolvation to rescore initial-stage docking predictions. Weights for the scoring terms were optimized for a set of test cases, and this optimized function was then tested on an independent set of nonredundant cases. This program, named ZRANK, is shown to significantly improve the success rate over the initial ZDOCK rankings across a large benchmark. The amount of test cases with No. 1 ranked hits increased from 2 to 11 and from 6 to 12 when predictions from two ZDOCK versions were considered. ZRANK can be applied either as a refinement protocol in itself or as a preprocessing stage to enrich the well-ranked hits prior to further refinement.
蛋白质-蛋白质对接需要快速有效的方法,以便迅速区分初始阶段对接产生的正确和错误预测。我们开发并测试了一种评分函数,该函数利用详细的静电作用、范德华力和去溶剂化作用对初始阶段的对接预测重新评分。针对一组测试案例对评分项的权重进行了优化,然后在一组独立的非冗余案例上对这个优化后的函数进行了测试。这个名为ZRANK的程序在一个大型基准测试中被证明比初始的ZDOCK排名显著提高了成功率。当考虑两个ZDOCK版本的预测时,排名第一的命中测试案例数量从2个增加到11个,从6个增加到12个。ZRANK既可以作为一种自身的优化协议应用,也可以作为一个预处理阶段,在进一步优化之前富集排名靠前的命中结果。