| Literature DB >> 26231283 |
Thom Vreven1, Iain H Moal2, Anna Vangone3, Brian G Pierce1, Panagiotis L Kastritis3, Mieczyslaw Torchala4, Raphael Chaleil4, Brian Jiménez-García2, Paul A Bates5, Juan Fernandez-Recio6, Alexandre M J J Bonvin7, Zhiping Weng8.
Abstract
We present an updated and integrated version of our widely used protein-protein docking and binding affinity benchmarks. The benchmarks consist of non-redundant, high-quality structures of protein-protein complexes along with the unbound structures of their components. Fifty-five new complexes were added to the docking benchmark, 35 of which have experimentally measured binding affinities. These updated docking and affinity benchmarks now contain 230 and 179 entries, respectively. In particular, the number of antibody-antigen complexes has increased significantly, by 67% and 74% in the docking and affinity benchmarks, respectively. We tested previously developed docking and affinity prediction algorithms on the new cases. Considering only the top 10 docking predictions per benchmark case, a prediction accuracy of 38% is achieved on all 55 cases and up to 50% for the 32 rigid-body cases only. Predicted affinity scores are found to correlate with experimental binding energies up to r=0.52 overall and r=0.72 for the rigid complexes.Entities:
Keywords: antibody–antigen; binding free energy; conformational change; protein–protein complex structure; protein–protein interface
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Year: 2015 PMID: 26231283 PMCID: PMC4677049 DOI: 10.1016/j.jmb.2015.07.016
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469