Inhibition of the DevSR Two-Component System by Overexpression of Mycobacterium tuberculosis PknB in Mycobacterium smegmatis

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dc.contributor.authorBae, Hyun-Jungko
dc.contributor.authorLee, Ha-Nako
dc.contributor.authorBaek, Mi-Nako
dc.contributor.authorPark, Eun-Jinko
dc.contributor.authorEom, Chi-Yongko
dc.contributor.authorKo, In-Jeongko
dc.contributor.authorKang, Ho-Youngko
dc.contributor.authorOh, Jeong-Ilko
dc.date.accessioned2017-12-19T03:04:37Z-
dc.date.available2017-12-19T03:04:37Z-
dc.date.created2017-12-11-
dc.date.created2017-12-11-
dc.date.issued2017-09-
dc.identifier.citationMOLECULES AND CELLS, v.40, no.9, pp.632 - 642-
dc.identifier.issn1016-8478-
dc.identifier.urihttp://hdl.handle.net/10203/228633-
dc.description.abstractThe DevSR (DosSR) two-component system, which is a major regulatory system involved in oxygen sensing in mycobacteria, plays an important role in hypoxic induction of many genes in mycobacteria. We demonstrated that overexpression of the kinase domain of Mycobacterium tuberculosis (Mtb) PknB inhibited transcriptional activity of the DevR response regulator in Mycobacterium smegmatis and that this inhibitory effect was exerted through phosphorylation of DevR on Thr180 within its DNA-binding domain. Moreover, the purified kinase domain of Mtb PknB significantly phosphorylated RegX3, NarL, KdpE, TrcR, DosR, and MtrA response regulators of Mtb that contain the Thr residues corresponding to Thr180 of DevR in their DNA-binding domains, implying that transcriptional activities of these response regulators might also be inhibited when the kinase domain of PknB is overexpressed.-
dc.languageEnglish-
dc.publisherKOREAN SOC MOLECULAR & CELLULAR BIOLOGY-
dc.subjectRESPONSE REGULATOR-
dc.subjectPROTEIN-KINASES-
dc.subjectSIGNAL-TRANSDUCTION-
dc.subjectHYPOXIC RESPONSE-
dc.subjectSERINE/THREONINE KINASES-
dc.subjectHISTIDINE KINASES-
dc.subjectGENE-EXPRESSION-
dc.subjectSER/THR-
dc.subjectGROWTH-
dc.subjectSENSOR-
dc.titleInhibition of the DevSR Two-Component System by Overexpression of Mycobacterium tuberculosis PknB in Mycobacterium smegmatis-
dc.typeArticle-
dc.identifier.wosid000416399300004-
dc.identifier.scopusid2-s2.0-85034014683-
dc.type.rimsART-
dc.citation.volume40-
dc.citation.issue9-
dc.citation.beginningpage632-
dc.citation.endingpage642-
dc.citation.publicationnameMOLECULES AND CELLS-
dc.identifier.doi10.14348/molcells.2017.0076-
dc.contributor.nonIdAuthorBae, Hyun-Jung-
dc.contributor.nonIdAuthorLee, Ha-Na-
dc.contributor.nonIdAuthorBaek, Mi-Na-
dc.contributor.nonIdAuthorPark, Eun-Jin-
dc.contributor.nonIdAuthorEom, Chi-Yong-
dc.contributor.nonIdAuthorKang, Ho-Young-
dc.contributor.nonIdAuthorOh, Jeong-Il-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorDevSR-
dc.subject.keywordAuthormycobacterium-
dc.subject.keywordAuthorSer/Thr protein kinase-
dc.subject.keywordAuthortwo-component system-
dc.subject.keywordPlusRESPONSE REGULATOR-
dc.subject.keywordPlusPROTEIN-KINASES-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusHYPOXIC RESPONSE-
dc.subject.keywordPlusSERINE/THREONINE KINASES-
dc.subject.keywordPlusHISTIDINE KINASES-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusSER/THR-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusSENSOR-
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