| Literature DB >> 20399133 |
Hongyong Fu1, Ya-Ling Lin, A S Fatimababy.
Abstract
Ubiquitin/26S proteasome-mediated proteolysis controls the half-life of numerous critical regulatory proteins and is an intimate regulatory component for nearly all aspects of cellular processes. In addition to ubiquitin conjugation, an additional level of substrate specificity is regulated at the step of proteasomal recognition of ubiquitylated substrates, which serves as an important mechanistic and regulatory component to connect the substrate from the conjugation machinery to the 26S proteasome. In this review, we discuss current knowledge and future challenges relevant to understanding the mechanism, regulation, functions and substrate specificity of proteasomal recognition mediated by a multitude of ubiquitin receptors. The mechanistic details of major recognition pathways for ubiquitylated substrates are clearly divergent within and across species, which implies functional differentiation.Mesh:
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Year: 2010 PMID: 20399133 DOI: 10.1016/j.tplants.2010.03.004
Source DB: PubMed Journal: Trends Plant Sci ISSN: 1360-1385 Impact factor: 18.313