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PMID: 11076011 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Felix Hoppe-Seyler Lecture 2000. The ubiquitin system and the N-end rule pathway.

Biological chemistry ·Vol. 381 ·No. 9-10 ·2000-00-00 ·Pages 779-89

Varshavsky A, Turner G, Du F, Xie Y

Abstract

Eukaryotes contain a highly conserved multienzyme system which covalently links a small protein, ubiquitin, to a variety of intracellular proteins that bear degradation signals recognized by this system. The resulting ubiquitin-protein conjugates are degraded by the 26S proteasome, an ATP-dependent protease. Pathways that involve ubiquitin play major roles in a huge variety of processes, including cell differentiation, cell cycle, and responses to stress. In this article we briefly review the design of the ubiquitin system, and describe two recent advances, the finding that ubiquitin ligases interact with specific components of the 26S proteasome, and the demonstration that peptides accelerate their uptake into cells by activating the N-end rule pathway, one of several proteolytic pathways of the ubiquitin system.

MeSH Terms
Animals Awards and Prizes Biochemical Phenomena Biochemistry Cell Physiological Phenomena Eukaryotic Cells/physiology Germany Humans Signal Transduction/physiology Ubiquitins/physiology
Chemicals
Ubiquitins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Varshavsky A
Division of Biology, California Institute of Technology, Pasadena 91125, USA.
Turner G
Du F
Xie Y
Article Info
Journal
Biological chemistry
Abbr.
Biol Chem
ISSN
1431-6730
Published
2000-00-00
Pages
779-89
Language
English
Region
Germany
NLM ID
9700112
Subset
IM
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