[Novel deglycosylation-independent roles for peptide N-glycanase]

Med Sci (Paris). 2014 Jan;30(1):47-54. doi: 10.1051/medsci/20143001013. Epub 2014 Jan 24.
[Article in French]

Abstract

The primary function of peptide N-glycanase (PNGase) is thought to be the deglycosylation of endoplasmic reticulum associated degradation (ERAD) substrates. However, inhibition of PNGase appears to have little effect upon the destruction rate of many ERAD substrates, and recent data demonstrate deglycosylation-independent functions for PNGase. Whatever the roles of PNGase turn out to be, the identification of a patient presenting with PNGase deficiency will advance our understanding of the importance of this multifunctional protein in human physiology.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Gene Expression
  • Glycosylation
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase / chemistry
  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase / physiology*
  • Protein Folding
  • Sequence Homology, Amino Acid
  • Tissue Distribution

Substances

  • Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase