4.7 Review

Ubiquitin-proteasome system - Ubiquitin-free routes into the proteasome

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 61, Issue 13, Pages 1596-1600

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-004-4133-9

Keywords

proteasome; proteolysis; ubiquitin-independent; ornithine decarboxylase; antizyme; I kappa B alpha; c-Jun

Ask authors/readers for more resources

The majority of proteasome substrates identified to date are marked for degradation by polyubiquitinylation. Exceptions to this principle, however, are well documented and can help us understand the process proteasomes use to recognize their substrates. Examples include ornithine decarboxylase, p21/Cip1, TCRalpha, IkappaBalpha, c-Jun, calmodulin and thymidylate synthase. Degradation of these proteins can be completely ubiquitin-independent or coexist with ubiquitin-dependent pathways. Uncoupling degradation from ubiquitin modification may reflect the evolutionary conservation of mechanisms optimized for highly specialized regulatory functions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available