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dc.contributor.authorTone, Takuyaen
dc.contributor.authorNakayama, Kazuhisaen
dc.contributor.authorTakatsu, Hiroyukien
dc.contributor.authorShin, Hye Wonen
dc.contributor.alternative刀根, 卓也ja
dc.contributor.alternative中山, 和久ja
dc.contributor.alternative髙津, 宏之ja
dc.contributor.alternative申, 惠媛ja
dc.date.accessioned2020-03-05T04:16:29Z-
dc.date.available2020-03-05T04:16:29Z-
dc.date.issued2020-02-
dc.identifier.issn0014-5793-
dc.identifier.issn1873-3468-
dc.identifier.urihttp://hdl.handle.net/2433/245891-
dc.description.abstractP4‐ATPases belonging to the P‐type ATPase superfamily mediate active transport of phospholipids across cellular membranes. Most P4‐ATPases, except ATP9A and ATP9B proteins, form heteromeric complexes with CDC50 proteins, which are required for transport of P4‐ATPases from the endoplasmic reticulum (ER) to their final destinations. P‐type ATPases form autophosphorylated intermediates during the ATPase reaction cycle. However, the association of the catalytic cycle of P4‐ATPases with their transport from the ER and their cellular localization has not been studied. Here, we show that transport of ATP9 and ATP11 proteins as well as that of ATP10A from the ER depends on the ATPase catalytic cycle, suggesting that conformational changes in P4‐ATPases during the catalytic cycle are crucial for their transport from the ER.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWileyen
dc.rightsThis is the peer reviewed version of the following article: [FEBS Letters, 594(3), 415-423], which has been published in final form at https://doi.org/10.1002/1873-3468.13629. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en
dc.rightsThe full-text file will be made open to the public on 14 October 2020 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjectE1-E2 ATPaseen
dc.subjectflippaseen
dc.subjectlipid bilayeren
dc.subjectmembraneen
dc.subjectP4-ATPaseen
dc.titleATPase reaction cycle of P4-ATPases affects their transport from the endoplasmic reticulumen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA00642943-
dc.identifier.jtitleFEBS Lettersen
dc.identifier.volume594-
dc.identifier.issue3-
dc.identifier.spage412-
dc.identifier.epage423-
dc.relation.doi10.1002/1873-3468.13629-
dc.textversionauthor-
dc.addressDepartment of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressDepartment of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.identifier.pmid31571211-
dcterms.accessRightsopen access-
datacite.date.available2020-10-14-
datacite.awardNumber17H03655-
datacite.awardNumber17K08270-
dc.identifier.pissn0014-5793-
dc.identifier.eissn1873-3468-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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