Faculty of Chemistry and Chemical Biology, TU Dortmund University, Dortmund, Germany.
Department of Computer Science, TU Dortmund University, Dortmund, Germany.
PLoS Comput Biol. 2018 Nov 8;14(11):e1006483. doi: 10.1371/journal.pcbi.1006483. eCollection 2018 Nov.
The automated comparison of protein-ligand binding sites provides useful insights into yet unexplored site similarities. Various stages of computational and chemical biology research can benefit from this knowledge. The search for putative off-targets and the establishment of polypharmacological effects by comparing binding sites led to promising results for numerous projects. Although many cavity comparison methods are available, a comprehensive analysis to guide the choice of a tool for a specific application is wanting. Moreover, the broad variety of binding site modeling approaches, comparison algorithms, and scoring metrics impedes this choice. Herein, we aim to elucidate strengths and weaknesses of binding site comparison methodologies. A detailed benchmark study is the only possibility to rationalize the selection of appropriate tools for different scenarios. Specific evaluation data sets were developed to shed light on multiple aspects of binding site comparison. An assembly of all applied benchmark sets (ProSPECCTs-Protein Site Pairs for the Evaluation of Cavity Comparison Tools) is made available for the evaluation and optimization of further and still emerging methods. The results indicate the importance of such analyses to facilitate the choice of a methodology that complies with the requirements of a specific scientific challenge.
蛋白质-配体结合位点的自动比较为尚未探索的位点相似性提供了有用的见解。计算和化学生物学研究的各个阶段都可以从这些知识中受益。通过比较结合位点来寻找潜在的脱靶效应和建立多效性作用,为许多项目带来了有希望的结果。尽管有许多腔比较方法可用,但缺乏全面的分析来指导为特定应用选择工具。此外,广泛的结合位点建模方法、比较算法和评分指标阻碍了这种选择。在这里,我们旨在阐明结合位点比较方法的优缺点。详细的基准研究是为不同情况合理选择合适工具的唯一可能性。还开发了特定的评估数据集,以阐明结合位点比较的多个方面。所有应用基准集(ProSPECCTs-用于评估腔比较工具的蛋白质位点对)的集合都可用于评估和优化进一步和新兴的方法。结果表明,这种分析对于促进选择符合特定科学挑战要求的方法非常重要。