4.3 Review

gp78: a Multifaceted Ubiquitin Ligase that Integrates a Unique Protein Degradation Pathway from the Endoplasmic Reticulum

Journal

CURRENT PROTEIN & PEPTIDE SCIENCE
Volume 13, Issue 5, Pages 414-424

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138920312802430590

Keywords

ubiquitination; retrotranslocation/dislocation; E3 ubiquitin ligase; gp78; Hrd1; p97/VCP; proteasome; endoplasmic reticulum; and ER-associated degradation

Funding

  1. NIH [GM06696]
  2. NSF [1120833]

Ask authors/readers for more resources

The endoplasmic reticulum (ER) is the site for maturation of proteins destined for the secretory pathway. Failure in maturation leads to production of misfolded proteins that are eliminated through the ER-associated degradation (ERAD) pathway. ERAD is a complex process that includes misfolded protein recognition, retrotranslocation to the cytosol, ubiquitination and proteasomal degradation. gp78 is an E3 ubiquitin ligase that integrates these ERAD steps by nucleating a unique degradation machine, which uses the p97/VCP-Npl4 complex for retrotranslocation instead of the well-known p97/VCP-Ufd1-Npl4 complex. A growing list of substrates have been identified for gp78, which highlights the importance of gp78-mediated ERAD in essential physiological pathways and pathological processes.

Authors

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

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available