Atomic-level evolutionary information improves protein-protein interface scoring

被引:3
作者
Quignot, Chloe [1 ]
Granger, Pierre [1 ]
Chacon, Pablo [2 ]
Guerois, Raphael [1 ]
Andreani, Jessica [1 ]
机构
[1] Univ Paris Saclay, Inst Integrat Biol Cell I2BC, CNRS, CEA, F-91198 Gif Sur Yvette, France
[2] Rocasolano Inst Phys Chem CSIC, Dept Biol Chem Phys, Serrano 119, Madrid 28006, Spain
关键词
DOCKING; PREDICTIONS; SERVER;
D O I
10.1093/bioinformatics/btab254
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: The crucial role of protein interactions and the difficulty in characterizing them experimentally strongly motivates the development of computational approaches for structural prediction. Even when protein-protein docking samples correct models, current scoring functions struggle to discriminate them from incorrect decoys. The previous incorporation of conservation and coevolution information has shown promise for improving protein-protein scoring. Here, we present a novel strategy to integrate atomic-level evolutionary information into different types of scoring functions to improve their docking discrimination. Results: We applied this general strategy to our residue-level statistical potential from InterEvScore and to two atomic-level scores, SOAP-PP and Rosetta interface score (ISC). Including evolutionary information from as few as 10 homologous sequences improves the top 10 success rates of individual atomic-level scores SOAP-PP and Rosetta ISC by 6 and 13.5 percentage points, respectively, on a large benchmark of 752 docking cases. The best individual homology-enriched score reaches a top 10 success rate of 34.4%. A consensus approach based on the complementarity between different homology-enriched scores further increases the top 10 success rate to 40%.
引用
收藏
页码:3175 / 3181
页数:7
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