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dc.contributor.author김익태-
dc.contributor.author김낙균-
dc.contributor.author서정용-
dc.date.accessioned2024-01-19T22:01:14Z-
dc.date.available2024-01-19T22:01:14Z-
dc.date.created2021-09-06-
dc.date.issued2018-09-
dc.identifier.issn1226-6531-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/120951-
dc.description.abstractThe CRISPR-Cas system is the adaptive immune system in bacteria and archaea against invading phages or foreign plasmids. In the type II CRISPR-Cas system, an endonuclease Cas9 cleaves DNA targets of phages as directed by guide RNA comprising crRNA and tracrRNA. To avoid targeting and destruction by Cas9, phages employ anti-CRISPR (Acr) proteins that act against host bacterial immunity by inactivating the CRISPR-Cas system. Here we report the backbone 1H, 15N, and 13C resonance assignments of AcrIIA4 that inhibits endonuclease activity of type II-A Listeria monocytogenes Cas9 and also Streptococcus pyogenesis Cas9 using triple resonance nuclear magnetic resonance spectroscopy. The secondary structures of AcrIIA4 predicted by the backbone chemical shifts show an alpha-beta-beta-beta-alpha-alpha fold, which is used to determine the solution structure.-
dc.languageEnglish-
dc.publisher한국자기공명학회-
dc.title1H, 15N, and 13C Resonance Assignments of the Anti-CRISPR AcrIIA4 from Listeria monocytogenes Prophages-
dc.typeArticle-
dc.identifier.doi10.6564/JKMRS.2018.22.3.071-
dc.description.journalClass2-
dc.identifier.bibliographicCitationJournal of the Korean Magnetic Resonance Society, v.22, no.3, pp.71 - 75-
dc.citation.titleJournal of the Korean Magnetic Resonance Society-
dc.citation.volume22-
dc.citation.number3-
dc.citation.startPage71-
dc.citation.endPage75-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002384442-
dc.subject.keywordAuthorAcrIIA4-
dc.subject.keywordAuthoranti-CRISPR-
dc.subject.keywordAuthorCas9-
dc.subject.keywordAuthorNMR spectroscopy-
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