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Coevolution underlies GPCR-G protein selectivity and functionality
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dc.contributor.author Seo, Min Jae -
dc.contributor.author Heo, Joongyu -
dc.contributor.author Kim, Kyunghui -
dc.contributor.author Chung, Ka-young -
dc.contributor.author Yu, Wookyung -
dc.date.accessioned 2021-09-27T11:30:02Z -
dc.date.available 2021-09-27T11:30:02Z -
dc.date.created 2021-04-30 -
dc.date.issued 2021-04 -
dc.identifier.citation Scientific Reports, v.11, no.1, pp.7858 - 154 -
dc.identifier.issn 2045-2322 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/15330 -
dc.description.abstract G protein-coupled receptors (GPCRs) regulate diverse physiological events, which makes them as the major targets for many approved drugs. G proteins are downstream molecules that receive signals from GPCRs and trigger cell responses. The GPCR-G protein selectivity mechanism on how they properly and timely interact is still unclear. Here, we analyzed model GPCRs (i.e. HTR, DAR) and Gα proteins with a coevolutionary tool, statistical coupling analysis. The results suggested that 5-hydroxytryptamine receptors and dopamine receptors have common conserved and coevolved residues. The Gα protein also have conserved and coevolved residues. These coevolved residues were implicated in the molecular functions of the analyzed proteins. We also found specific coevolving pairs related to the selectivity between GPCR and G protein were identified. We propose that these results would contribute to better understandings of not only the functional residues of GPCRs and Gα proteins but also GPCR-G protein selectivity mechanisms. © 2021, The Author(s). -
dc.language English -
dc.publisher Nature Publishing Group -
dc.title Coevolution underlies GPCR-G protein selectivity and functionality -
dc.type Article -
dc.identifier.doi 10.1038/s41598-021-87251-6 -
dc.identifier.wosid 000640428900006 -
dc.identifier.scopusid 2-s2.0-85104245425 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.identifier.bibliographicCitation Seo, Min Jae. (2021-04). Coevolution underlies GPCR-G protein selectivity and functionality. doi: 10.1038/s41598-021-87251-6 -
dc.description.journalClass 1 -
dc.citation.publicationname Scientific Reports -
dc.contributor.nonIdAuthor Seo, Min Jae -
dc.contributor.nonIdAuthor Heo, Joongyu -
dc.contributor.nonIdAuthor Kim, Kyunghui -
dc.contributor.nonIdAuthor Chung, Ka-young -
dc.identifier.citationVolume 11 -
dc.identifier.citationNumber 1 -
dc.identifier.citationStartPage 7858 -
dc.identifier.citationEndPage 154 -
dc.identifier.citationTitle Scientific Reports -
dc.description.isOpenAccess Y -
dc.subject.keywordPlus STRUCTURAL BASIS -
dc.subject.keywordPlus COUPLED RECEPTORS -
dc.subject.keywordPlus ALPHA-SUBUNIT -
dc.subject.keywordPlus MOLECULAR SWITCHES -
dc.subject.keywordPlus SEQUENCE ALIGNMENT -
dc.subject.keywordPlus AMINO-ACIDS -
dc.subject.keywordPlus DETERMINANTS -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus SPECIFICITY -
dc.subject.keywordPlus TARGETS -
dc.contributor.affiliatedAuthor Seo, Min Jae -
dc.contributor.affiliatedAuthor Heo, Joongyu -
dc.contributor.affiliatedAuthor Kim, Kyunghui -
dc.contributor.affiliatedAuthor Chung, Ka-young -
dc.contributor.affiliatedAuthor Yu, Wookyung -
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