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- W1848935986 endingPage "mvw091" @default.
- W1848935986 startingPage "mvw091" @default.
- W1848935986 abstract "The 26S proteasome is a 2.5-MDa complex responsible for the selective, ATP-dependent degradation of ubiquitylated proteins in eukaryotic cells. Substrates in hundreds cellular pathways are timely ubiquitylated and converged to the proteasome by direct recognition or by multiple shuttle factors. Engagement of substrate protein triggers conformational changes of the proteasome, which drive substrate unfolding, deubiquitylation and translocation of substrates to proteolytic sites. Recent studies have challenged the previous paradigm that Lys48-linked tetraubiquitin is a minimal degradation signal: in addition, monoubiquitylation or multiple short ubiquitylations can serve as the targeting signal for proteasomal degradation. In this review, I highlight recent advances in our understanding of the proteasome structure, the ubiquitin topology in proteasome targeting, and the cellular factors that regulate proteasomal degradation." @default.
- W1848935986 created "2016-06-24" @default.
- W1848935986 creator A5018866207 @default.
- W1848935986 date "2017-01-08" @default.
- W1848935986 modified "2023-10-03" @default.
- W1848935986 title "Ubiquitin recognition by the proteasome" @default.
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