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PMID: 18438607 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

UBX domain proteins: major regulators of the AAA ATPase Cdc48/p97.

Cellular and molecular life sciences : CMLS ·Vol. 65 ·No. 15 ·2008-08-00 ·Pages 2360-71

Schuberth C, Buchberger A

Abstract

The highly conserved AAA ATPase Cdc48/p97 acts on ubiquitylated substrate proteins in cellular processes as diverse as the fusion of homotypic membranes and the degradation of misfolded proteins. The 'Ubiquitin regulatory X' (UBX) domain-containing proteins constitute the so far largest family of Cdc48/p97 cofactors. UBX proteins are involved in substrate recruitment to Cdc48/p97 and in the temporal and spatial regulation of its activity. In combination with UBX-like proteins and other cofactors, they can assemble into a large variety of Cdc48/p97-cofactor complexes possessing distinct cellular functions. This review gives an overview of the different subfamilies of UBX proteins and their functions, and discusses general principles of Cdc48/p97 regulation by these cofactors.

MeSH Terms
Adenosine Triphosphatases/metabolism Animals Cell Cycle Proteins/metabolism Humans Protein Structure, Secondary Protein Structure, Tertiary Proteins/chemistry,metabolism Ubiquitin/metabolism Valosin Containing Protein
Chemicals
Cell Cycle Proteins Proteins Ubiquitin Adenosine Triphosphatases Valosin Containing Protein
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Schuberth C
Cell Biology and Biophysics Unit, EMBL Heidelberg, Meyerhofstrasse 1, Heidelberg, Germany. schubert@embl.de
Buchberger A
Article Info
Journal
Cellular and molecular life sciences : CMLS
Abbr.
Cell Mol Life Sci
ISSN
1420-682X
Published
2008-08-00
Pages
2360-71
Language
English
Region
Switzerland
NLM ID
9705402
Subset
IM
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