| Literature DB >> 24457024 |
Gary Kleiger1, Thibault Mayor2.
Abstract
Eukaryotic cells are equipped to degrade proteins via the ubiquitin-proteasome system (UPS). Proteins become degraded upon their conjugation to chains of ubiquitin where they are then directed to the 26S proteasome, a macromolecular protease. The transfer of ubiquitin to proteins and their subsequent degradation are highly complex processes, and new research is beginning to uncover the molecular details of how ubiquitination and degradation take place in the cell. We review some of the new data providing insights into how these processes occur. Although distinct mechanisms are often observed, some common themes are emerging for how the UPS guides protein substrates through their final journey.Entities:
Keywords: E1-activating; E2-conjugating; E3-ligase; proteolysis; ubiquitin proteasome system
Mesh:
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Year: 2014 PMID: 24457024 PMCID: PMC4037451 DOI: 10.1016/j.tcb.2013.12.003
Source DB: PubMed Journal: Trends Cell Biol ISSN: 0962-8924 Impact factor: 20.808