Integrative genome-scale metabolic analysis of Vibrio vulnificus for drug targeting and discovery

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dc.contributor.authorH U Kim-
dc.contributor.authorS Y Kim-
dc.contributor.authorHaeyoung Jeong-
dc.contributor.authorT Y Kim-
dc.contributor.authorJ J Kim-
dc.contributor.authorH E Choy-
dc.contributor.authorK Y Yi-
dc.contributor.authorJ H Rhee-
dc.contributor.authorS Y Lee-
dc.date.accessioned2017-04-19T09:21:17Z-
dc.date.available2017-04-19T09:21:17Z-
dc.date.issued2011-
dc.identifier.issn1744-4292-
dc.identifier.uri10.1038/msb.2010.115ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/9951-
dc.description.abstractAlthough the genomes of many microbial pathogens have been studied to help identify effective drug targets and novel drugs, such efforts have not yet reached full fruition. In this study, we report a systems biological approach that efficiently utilizes genomic information for drug targeting and discovery, and apply this approach to the opportunistic pathogen Vibrio vulnificus CMCP6. First, we partially re-sequenced and fully re-annotated the V. vulnificus CMCP6 genome, and accordingly reconstructed its genome-scale metabolic network, VvuMBEL943. The validated network model was employed to systematically predict drug targets using the concept of metabolite essentiality, along with additional filtering criteria. Target genes encoding enzymes that interact with the five essential metabolites finally selected were experimentally validated. These five essential metabolites are critical to the survival of the cell, and hence were used to guide the cost-effective selection of chemical analogs, which were then screened for antimicrobial activity in a whole-cell assay. This approach is expected to help fill the existing gap between genomics and drug discovery.-
dc.publisherWiley-
dc.titleIntegrative genome-scale metabolic analysis of Vibrio vulnificus for drug targeting and discovery-
dc.title.alternativeIntegrative genome-scale metabolic analysis of Vibrio vulnificus for drug targeting and discovery-
dc.typeArticle-
dc.citation.titleMolecular Systems Biology-
dc.citation.number0-
dc.citation.endPage460-
dc.citation.startPage460-
dc.citation.volume7-
dc.contributor.affiliatedAuthorHaeyoung Jeong-
dc.contributor.alternativeName김현욱-
dc.contributor.alternativeName김수영-
dc.contributor.alternativeName정해영-
dc.contributor.alternativeName김태용-
dc.contributor.alternativeName김재종-
dc.contributor.alternativeName최현-
dc.contributor.alternativeName이규양-
dc.contributor.alternativeName이준행-
dc.contributor.alternativeName이상엽-
dc.identifier.bibliographicCitationMolecular Systems Biology, vol. 7, pp. 460-460-
dc.identifier.doi10.1038/msb.2010.115-
dc.subject.keyworddrug discovery-
dc.subject.keyworddrug targeting-
dc.subject.keywordgenome analysis-
dc.subject.keywordmetabolic network-
dc.subject.keywordVibrio vulnificus-
dc.subject.localDrug discovery-
dc.subject.localdrug discovery-
dc.subject.localDrug Discovery-
dc.subject.localdrug targeting-
dc.subject.localgenome analyses-
dc.subject.localgenome analysis-
dc.subject.localGenome analysis-
dc.subject.localmetabolic network-
dc.subject.localvibrio vulnificus-
dc.subject.localVibrio vulnificus-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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