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LigDockCSA: Protein–ligand docking using conformational space annealing
Author(s) -
Shin WoongHee,
Heo Lim,
Lee Juyong,
Ko Junsu,
Seok Chaok,
Lee Jooyoung
Publication year - 2011
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.21905
Subject(s) - autodock , docking (animal) , simulated annealing , protein–ligand docking , computer science , algorithm , virtual screening , computational chemistry , chemistry , in silico , molecular dynamics , biochemistry , medicine , nursing , gene
Protein–ligand docking techniques are one of the essential tools for structure‐based drug design. Two major components of a successful docking program are an efficient search method and an accurate scoring function. In this work, a new docking method called LigDockCSA is developed by using a powerful global optimization technique, conformational space annealing (CSA), and a scoring function that combines the AutoDock energy and the piecewise linear potential (PLP) torsion energy. It is shown that the CSA search method can find lower energy binding poses than the Lamarckian genetic algorithm of AutoDock. However, lower‐energy solutions CSA produced with the AutoDock energy were often less native‐like. The loophole in the AutoDock energy was fixed by adding a torsional energy term, and the CSA search on the refined energy function is shown to improve the docking performance. The performance of LigDockCSA was tested on the Astex diverse set which consists of 85 protein–ligand complexes. LigDockCSA finds the best scoring poses within 2 Å root‐mean‐square deviation (RMSD) from the native structures for 84.7% of the test cases, compared to 81.7% for AutoDock and 80.5% for GOLD. The results improve further to 89.4% by incorporating the conformational entropy. © 2011 Wiley Periodicals, Inc. J Comput Chem, 2011