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The cytoplasmic peptide:N-glycanase (NGLY1) - Structure, expression and cellular functions.
- Source :
-
Gene [Gene] 2016 Feb 10; Vol. 577 (1), pp. 1-7. Date of Electronic Publication: 2015 Nov 30. - Publication Year :
- 2016
-
Abstract
- NGLY1/Ngly1 is a cytosolic peptide:N-glycanase, i.e. de-N-glycosylating enzyme acting on N-glycoproteins in mammals, generating free, unconjugated N-glycans and deglycosylated peptides in which the N-glycosylated asparagine residues are converted to aspartates. This enzyme is known to be involved in the quality control system for the newly synthesized glycoproteins in the endoplasmic reticulum (ER). In this system, misfolded (glyco)proteins are retrotranslocated to the cytosol, where the 26S proteasomes play a central role in degrading the proteins: a process referred to as ER-associated degradation or ERAD in short. PNGase-mediated deglycosylation is believed to facilitate the efficient degradation of some misfolded glycoproteins. Human patients harboring mutations of NGLY1 gene (NGLY1-deficiency) have recently been discovered, clearly indicating the functional importance of this enzyme. This review summarizes the current state of our knowledge on NGLY1 and its gene product in mammalian cells.<br /> (Copyright © 2015 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Asparagine genetics
Cytosol metabolism
Endoplasmic Reticulum metabolism
Glycoproteins genetics
Glycoproteins metabolism
Glycosylation
Humans
Mammals
Mutation
Peptides metabolism
Polysaccharides metabolism
Proteasome Endopeptidase Complex genetics
Proteasome Endopeptidase Complex metabolism
Endoplasmic Reticulum-Associated Degradation
Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase chemistry
Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase genetics
Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0038
- Volume :
- 577
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Gene
- Publication Type :
- Academic Journal
- Accession number :
- 26611529
- Full Text :
- https://doi.org/10.1016/j.gene.2015.11.021