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dc.contributor.authorBoom, Johannes van den-
dc.date.accessioned2023-11-22T02:51:38Z-
dc.date.available2023-11-22T02:51:38Z-
dc.date.issued2023-
dc.identifier.otherOER000002677vi
dc.identifier.urihttp://dlib.hust.edu.vn/handle/HUST/23541-
dc.description.abstractThe AAA+ ATPase p97 (also called VCP, or Cdc48 in yeast) unfolds proteins and disassembles protein complexes in a myriad of cellular processes, but how a substrate complex needs to be loaded onto p97 by a dedicated substrate adapter and then disassembled by p97 has not been structurally visualized so far. Here we present cryo-EM structures of p97 in the process of disassembling a protein phosphatase-1 (PP1) complex by stripping off an inhibitory subunit. We show that PP1 and its partners SDS22 and inhibitor-3 (I3) bind to a peripheral N-domain of p97 via a direct contact between SDS22 and a groove in the N-domain. A density consistent with the SHP box of the p37 adapter binds to the same N-domain underneath the PP1 complex, while the p37-UBX domain is found on the adjacent N-domain. I3 is likely represented by three densities.vi
dc.description.urihttps://www.biorxiv.org/content/10.1101/2022.06.24.497491v1.full.pdf+htmlvi
dc.formatPDFvi
dc.language.isoenvi
dc.publisherbioRxivvi
dc.subjectCơ sở cấu trúcvi
dc.subjectubiquitinvi
dc.subjectphân táchvi
dc.subjectphức hợpvi
dc.subjectPP1 độc lậpvi
dc.subject.lccRC683.5vi
dc.titleStructural basis of ubiquitin-independent PP1 complex disassembly by p97vi
dc.typeJournal articlevi
dc.description.noteCC-BY-NC-4.0vi
Appears in Collections:OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường

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