reviewAnnual Review of BiochemistryJun 1, 2009Closed access

Recognition and Processing of Ubiquitin-Protein Conjugates by the Proteasome

Harvard University

PubMed
Indexed incrossrefpubmed

Abstract

The proteasome is an intricate molecular machine, which serves to degrade proteins following their conjugation to ubiquitin. Substrates dock onto the proteasome at its 19-subunit regulatory particle via a diverse set of ubiquitin receptors and are then translocated into an internal chamber within the 28-subunit proteolytic core particle (CP), where they are hydrolyzed. Substrate is threaded into the CP through a narrow gated channel, and thus translocation requires unfolding of the substrate. Six distinct ATPases in the regulatory particle appear to form a ring complex and to drive unfolding as well as translocation. ATP-dependent, degradation-coupled deubiquitination of the substrate is required both for…

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Authors

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Topics & keywords

Keywords
  • Ubiquitin
  • Proteasome
  • Deubiquitinating enzyme
  • Protein subunit
  • Protein degradation
  • Ubiquitin-conjugating enzyme
  • Proteolysis
  • AAA proteins
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