Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/107252
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Electrical and Electronic Engineeringen_US
dc.creatorWong, GYen_US
dc.creatorLeung, FHFen_US
dc.creatorLing, SSHen_US
dc.date.accessioned2024-06-13T01:04:54Z-
dc.date.available2024-06-13T01:04:54Z-
dc.identifier.isbn978-1-5090-3474-1 (Electronic)en_US
dc.identifier.isbn978-1-5090-3475-8 (Print on Demand(PoD))en_US
dc.identifier.urihttp://hdl.handle.net/10397/107252-
dc.descriptionIECON 2016 - 42nd Annual Conference of the IEEE Industrial Electronics Society, 23-26 October 2016, Florence, Italyen_US
dc.language.isoenen_US
dc.publisherInstitute of Electrical and Electronics Engineersen_US
dc.rights©2016 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other works.en_US
dc.rightsThe following publication G. Y. Wong, F. H. F. Leung and S. S. H. Ling, "Identification of protein-ligand binding site using multi-clustering and Support Vector Machine," IECON 2016 - 42nd Annual Conference of the IEEE Industrial Electronics Society, Florence, Italy, 2016, pp. 939-944 is available at https://doi.org/10.1109/IECON.2016.7793821.en_US
dc.subjectMulti-clusteringen_US
dc.subjectProtein-ligand binding siteen_US
dc.subjectSVMen_US
dc.titleIdentification of protein-ligand binding site using multi-clustering and Support Vector Machineen_US
dc.typeConference Paperen_US
dc.identifier.spage939en_US
dc.identifier.epage944en_US
dc.identifier.doi10.1109/IECON.2016.7793821en_US
dcterms.abstractMulti-clustering has been widely used. It acts as a pre-training process for identifying protein-ligand binding in structure-based drug design. Then, the Support Vector Machine (SVM) is employed to classify the sites most likely for binding ligands. Three types of attributes are used, namely geometry-based, energy-based, and sequence conservation. Comparison is made on 198 drug-target protein complexes with LIGSITECSC, SURFNET, Fpocket, Q-SiteFinder, ConCavity, and MetaPocket. The results show an improved success rate of up to 86%.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationIn Proceedings of IECON 2016 - 42nd Annual Conference of the IEEE Industrial Electronics Society, 23-26 October 2016, Florence, Italy, p. 939-944en_US
dcterms.issued2016-
dc.identifier.scopus2-s2.0-85010064666-
dc.relation.conferenceAnnual Conference of the IEEE Industrial Electronics Society [IECON]en_US
dc.description.validate202404 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberEIE-0784-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS9586672-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Conference Paper
Files in This Item:
File Description SizeFormat 
Leung_Identification_Protein-Ligand_Binding.pdfPre-Published version507.9 kBAdobe PDFView/Open
Open Access Information
Status open access
File Version Final Accepted Manuscript
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Page views

7
Citations as of Jun 30, 2024

SCOPUSTM   
Citations

3
Citations as of Jun 21, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.