Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.11861/7523
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, Hongjian | en_US |
dc.contributor.author | Prof. LEUNG Kwong Sak | en_US |
dc.contributor.author | Wong, Man-Hon | en_US |
dc.date.accessioned | 2023-03-17T04:25:27Z | - |
dc.date.available | 2023-03-17T04:25:27Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | 2012 IEEE Symposium on Computational Intelligence and Computational Biology, CIBCB 2012 6217214, pp. 77-84 | en_US |
dc.identifier.isbn | 978-146731189-2 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11861/7523 | - |
dc.description.abstract | AutoDock Vina is a competitive protein-ligand docking tool well known for its fast execution and high accuracy. Nevertheless, when docking a massive number of ligands, Vina has to be run multiple times, repeating receptor parsing and grid maps building over and over again. There are tremendous requests for revising Vina to reuse precalculated data and incorporate built-in support for virtual screening. Hence we developed idock, inheriting from AutoDock Vina the accurate scoring function and the efficient optimization algorithm, and significantly improving the fundamental implementation and numerical model for even faster execution. idock achieves a speedup of 3.3 in terms of CPU time and a speedup of 7.5 in terms of elapsed time on average. idock is free and open source, available at https://GitHub.com/HongjianLi/idock. © 2012 IEEE. | en_US |
dc.description.sponsorship | IEEE Computational Intelligence Society | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | 2012 IEEE Symposium on Computational Intelligence and Computational Biology, CIBCB | en_US |
dc.title | Idock: A multithreaded virtual screening tool for flexible ligand docking | en_US |
dc.type | Conference Paper | en_US |
dc.identifier.doi | 10.1109/CIBCB.2012.6217214 | - |
item.fulltext | No Fulltext | - |
crisitem.author.dept | Department of Applied Data Science | - |
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