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Comparative Assessment of Scoring Functions on a Diverse Test Set

排名(信息检索) 虚拟筛选 试验装置 对接(动物) 计算机科学 数据挖掘 数学 人工智能 计算生物学 药物发现 生物 生物信息学 医学 护理部
作者
Tiejun Cheng,Xun Li,Yan Li,Zhihai Liu,Renxiao Wang
出处
期刊:Journal of Chemical Information and Modeling [American Chemical Society]
卷期号:49 (4): 1079-1093 被引量:481
标识
DOI:10.1021/ci9000053
摘要

Scoring functions are widely applied to the evaluation of protein−ligand binding in structure-based drug design. We have conducted a comparative assessment of 16 popular scoring functions implemented in main-stream commercial software or released by academic research groups. A set of 195 diverse protein−ligand complexes with high-resolution crystal structures and reliable binding constants were selected through a systematic nonredundant sampling of the PDBbind database and used as the primary test set in our study. All scoring functions were evaluated in three aspects, that is, "docking power", "ranking power", and "scoring power", and all evaluations were independent from the context of molecular docking or virtual screening. As for "docking power", six scoring functions, including GOLD::ASP, DS::PLP1, DrugScorePDB, GlideScore-SP, DS::LigScore, and GOLD::ChemScore, achieved success rates over 70% when the acceptance cutoff was root-mean-square deviation < 2.0 Å. Combining these scoring functions into consensus scoring schemes improved the success rates to 80% or even higher. As for "ranking power" and "scoring power", the top four scoring functions on the primary test set were X-Score, DrugScoreCSD, DS::PLP, and SYBYL::ChemScore. They were able to correctly rank the protein−ligand complexes containing the same type of protein with success rates around 50%. Correlation coefficients between the experimental binding constants and the binding scores computed by these scoring functions ranged from 0.545 to 0.644. Besides the primary test set, each scoring function was also tested on four additional test sets, each consisting of a certain number of protein−ligand complexes containing one particular type of protein. Our study serves as an updated benchmark for evaluating the general performance of today's scoring functions. Our results indicate that no single scoring function consistently outperforms others in all three aspects. Thus, it is important in practice to choose the appropriate scoring functions for different purposes.
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