| Literature DB >> 28525752 |
Galen Andrew Collins1, Alfred L Goldberg2.
Abstract
The ubiquitin proteasome pathway is responsible for most of the protein degradation in mammalian cells. Rates of degradation by this pathway have generally been assumed to be determined by rates of ubiquitylation. However, recent studies indicate that proteasome function is also tightly regulated and determines whether a ubiquitylated protein is destroyed or deubiquitylated and survives longer. This article reviews recent advances in our understanding of the proteasome's multistep ATP-dependent mechanism, its biochemical and structural features that ensure efficient proteolysis and ubiquitin recycling while preventing nonselective proteolysis, and the regulation of proteasome activity by interacting proteins and subunit modifications, especially phosphorylation.Entities:
Keywords: proteasome phosphorylation; protein degradation; protein turnover; ubiquitin proteasome system
Mesh:
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Year: 2017 PMID: 28525752 PMCID: PMC5609836 DOI: 10.1016/j.cell.2017.04.023
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582