| Literature DB >> 29101520 |
Dzmitry Padhorny1,2, David R Hall3, Hanieh Mirzaei4, Artem B Mamonov4, Mohammad Moghadasi4, Andrey Alekseenko5,6, Dmitri Beglov7, Dima Kozakov8,9.
Abstract
Fast Fourier transform (FFT) based approaches have been successful in application to modeling of relatively rigid protein-protein complexes. Recently, we have been able to adapt the FFT methodology to treatment of flexible protein-peptide interactions. Here, we report our latest attempt to expand the capabilities of the FFT approach to treatment of flexible protein-ligand interactions in application to the D3R PL-2016-1 challenge. Based on the D3R assessment, our FFT approach in conjunction with Monte Carlo minimization off-grid refinement was among the top performing methods in the challenge. The potential advantage of our method is its ability to globally sample the protein-ligand interaction landscape, which will be explored in further applications.Entities:
Keywords: D3R; Drug design data resource; FFT sampling; Protein ligand docking
Mesh:
Substances:
Year: 2017 PMID: 29101520 PMCID: PMC5767528 DOI: 10.1007/s10822-017-0069-7
Source DB: PubMed Journal: J Comput Aided Mol Des ISSN: 0920-654X Impact factor: 3.686