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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Boom, Johannes van den | - |
dc.date.accessioned | 2023-11-22T02:51:38Z | - |
dc.date.available | 2023-11-22T02:51:38Z | - |
dc.date.issued | 2023 | - |
dc.identifier.other | OER000002677 | vi |
dc.identifier.uri | http://dlib.hust.edu.vn/handle/HUST/23541 | - |
dc.description.abstract | The 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.uri | https://www.biorxiv.org/content/10.1101/2022.06.24.497491v1.full.pdf+html | vi |
dc.format | vi | |
dc.language.iso | en | vi |
dc.publisher | bioRxiv | vi |
dc.subject | Cơ sở cấu trúc | vi |
dc.subject | ubiquitin | vi |
dc.subject | phân tách | vi |
dc.subject | phức hợp | vi |
dc.subject | PP1 độc lập | vi |
dc.subject.lcc | RC683.5 | vi |
dc.title | Structural basis of ubiquitin-independent PP1 complex disassembly by p97 | vi |
dc.type | Journal article | vi |
dc.description.note | CC-BY-NC-4.0 | vi |
Appears in Collections: | OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường |
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