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dc.contributor.authorYang, JMen_US
dc.contributor.authorShen, TWen_US
dc.contributor.authorChen, YFen_US
dc.contributor.authorChiu, YYen_US
dc.date.accessioned2014-12-08T15:39:49Z-
dc.date.available2014-12-08T15:39:49Z-
dc.date.issued2004en_US
dc.identifier.isbn3-540-22344-4en_US
dc.identifier.issn0302-9743en_US
dc.identifier.urihttp://hdl.handle.net/11536/27202-
dc.description.abstractWe have developed a new tool for virtual database screening. This tool, referred to as the Generic Evolutionary Method for molecular DOCKing (GEMDOCK), combines an evolutionary approach and a new pharmacophore-based scoring function. The former integrates discrete and continuous global search strategies with local search strategies to speed up convergence. The latter simultaneously serves as the scoring function of both molecular docking and post-docking analysis to improve the number of the true positives. We accessed the accuracy of our approach on HSV-1 thymidine kinase using a ligand database on which competing tools were evaluated. The accuracies of our predictions were 0.54 for the GH score and 1.62% for the false positive rate when the true positive rate was 100%. We found that our pharmacophore-based scoring function indeed is able to reduce the number of the false positives. These results suggest that GEMDOCK is robust and can be a useful tool for virtual database screening.en_US
dc.language.isoen_USen_US
dc.titleAn evolutionary approach with pharmacophore-based scoring functions for virtual database screeningen_US
dc.typeArticle; Proceedings Paperen_US
dc.identifier.journalGENETIC AND EVOLUTIONARY COMPUTATION - GECCO 2004, PT 1, PROCEEDINGSen_US
dc.citation.volume3102en_US
dc.citation.spage481en_US
dc.citation.epage492en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000225101200048-
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