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首页> 外文期刊>Proteins: Structure, Function, and Genetics >A detailed comparison of current docking and scoring methods on systems of pharmaceutical relevance.
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A detailed comparison of current docking and scoring methods on systems of pharmaceutical relevance.

机译:当前对接和评分方法在药物相关系统上的详细比较。

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A thorough evaluation of some of the most advanced docking and scoring methods currently available is described, and guidelines for the choice of an appropriate protocol for docking and virtual screening are defined. The generation of a large and highly curated test set of pharmaceutically relevant protein-ligand complexes with known binding affinities is described, and three highly regarded docking programs (Glide, GOLD, and ICM) are evaluated on the same set with respect to their ability to reproduce crystallographic binding orientations. Glide correctly identified the crystallographic pose within 2.0 A in 61% of the cases, versus 48% for GOLD and 45% for ICM. In general Glide appears to perform most consistently with respect to diversity of binding sites and ligand flexibility, while the performance of ICM and GOLD is more binding site-dependent and it is significantly poorer when binding is predominantly driven by hydrophobic interactions. The results also show that energy minimization and reranking of the top N poses can be an effective means to overcome some of the limitations of a given docking function. The same docking programs are evaluated in conjunction with three different scoring functions for their ability to discriminate actives from inactives in virtual screening. The evaluation, performed on three different systems (HIV-1 protease, IMPDH, and p38 MAP kinase), confirms that the relative performance of different docking and scoring methods is to some extent binding site-dependent. GlideScore appears to be an effective scoring function for database screening, with consistent performance across several types of binding sites, while ChemScore appears to be most useful in sterically demanding sites since it is more forgiving of repulsive interactions. Energy minimization of docked poses can significantly improve the enrichments in systems with sterically demanding binding sites. Overall Glide appears to be a safe general choice for docking, while the choice of the best scoring tool remains to a larger extent system-dependent and should be evaluated on a case-by-case basis.
机译:描述了对当前可用的一些最先进的对接和评分方法的全面评估,并定义了用于选择对接和虚拟筛选的适当协议的指南。描述了具有已知结合亲和力的药物相关的蛋白质-配体复合物的大型且高度精确的测试集的生成,并针对同一集对三种高度评价的对接程序(Glide,GOLD和ICM)进行了评估重现晶体学结合方向。 Glide在61%的情况下正确识别出2.0 A以内的晶体姿势,而GOLD为48%,ICM为45%。通常,在结合位点的多样性和配体柔韧性方面,Glide表现出最一致的表现,而ICM和GOLD的表现更依赖于结合位点,而当结合主要​​由疏水相互作用驱动时,其性能会大大降低。结果还表明,最小化前N个姿势的能量和重新排序可能是克服给定对接功能的某些限制的有效方法。将相同的对接程序与三个不同的评分功能结合起来,以评估它们在虚拟筛选中区分有效成分和无效成分的能力。对三种不同系统(HIV-1蛋白酶,IMPDH和p38 MAP激酶)进行的评估证实,不同对接和评分方法的相对性能在一定程度上取决于结合位点。 GlideScore似乎是一种有效的数据库筛选评分功能,在几种类型的结合位点上均具有一致的性能,而ChemScore似乎在空间要求严格的位点上最有用,因为它更能排斥排斥性相互作用。对接姿势的能量最小化可以显着改善具有空间要求的结合位点的系统的富集。总体滑行似乎是对接的安全通用选择,而最佳评分工具的选择在很大程度上仍取决于系统,因此应逐案评估。

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