Homo sapiens Protein: NGLY1
Summary
InnateDB Protein IDBP-22698.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NGLY1
Protein Name N-glycanase 1
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000307980
InnateDB Gene IDBG-22696 (NGLY1)
Protein Structure
UniProt Annotation
Function Specifically deglycosylates the denatured form of N- linked glycoproteins in the cytoplasm and assists their proteasome-mediated degradation. Cleaves the beta-aspartyl- glucosamine (GlcNAc) of the glycan and the amide side chain of Asn, converting Asn to Asp. Prefers proteins containing high- mannose over those bearing complex type oligosaccharides. Can recognize misfolded proteins in the endoplasmic reticulum that are exported to the cytosol to be destroyed and deglycosylate them, while it has no activity toward native proteins. Deglycosylation is a prerequisite for subsequent proteasome-mediated degradation of some, but not all, misfolded glycoproteins. {ECO:0000269PubMed:14749736, ECO:0000269PubMed:15358861}.
Subcellular Localization Cytoplasm {ECO:0000269PubMed:15358861}.
Disease Associations Congenital disorder of glycosylation 1V (CDG1V) [MIM:615273]: A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Characterized by developmental delay, hypotonia, abnormal involuntary movements and alacrima or poor tear production. Other features include microcephaly, intractable seizures, abnormal eye movements and evidence of liver dysfunction, probably due to cytoplasmic accumulation of storage material in vacuoles. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. {ECO:0000269PubMed:22581936, ECO:0000269PubMed:24651605}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 18 experimentally validated interaction(s) in this database.
They are also associated with 9 interaction(s) predicted by orthology.
Experimentally validated
Total 18 [view]
Protein-Protein 17 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 9 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000224 peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase activity
GO:0005515 protein binding
GO:0046872 metal ion binding
Biological Process
GO:0006516 glycoprotein catabolic process
Cellular Component
GO:0005737 cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR002931 Transglutaminase-like
IPR006567 PUG domain
IPR006588 Peptide N glycanase, PAW domain
IPR008979 Galactose-binding domain-like
IPR018997 PUB domain
PFAM PF01841
PF04721
PF09409
PRINTS
PIRSF
SMART SM00460
SM00580
SM00613
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96IV0
PhosphoSite PhosphoSite-Q96IV0
TrEMBL C9JU75
UniProt Splice Variant
Entrez Gene 55768
UniGene Hs.743367
RefSeq
HUGO HGNC:17646
OMIM 610661
CCDS
HPRD 10118
IMGT
EMBL AB209549 AC092798 AF250924 AK296047 BC000963 BC007226 BC017220
GenPept AAF74720 AAH00963 AAH07226 AAH17220 BAD92786 BAG58811