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alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase; beta-1,2-N-acetylglucosaminyltransferase II; GlcNAc-T II; GNT-II; mannoside acetylglucosaminyltransferase 2; N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase II (MGAT2)

Function: - catalyzes an essential step in the conversion of oligo- mannose to complex N-glycans - protein modification; protein glycosylation Compartment: - Golgi membrane - single-pass type 2 membrane protein Pathology: - defects in MGAT2 are the cause of congenital disorder of glycosylation type 2A

General

aminotransferase glycoprotein membrane protein

Properties

SIZE: entity length = 447 aa MW = 52 kD COMPARTMENT: golgi MOTIF: transmembrane domain {10-29} N-glycosylation site {N69} N-glycosylation site {N86}

Database Correlations

OMIM correlations MORBIDMAP 602616 UniProt Q10469 Pfam PF05060 Entrez Gene 4247 Kegg hsa:4247 ENZYME 2.4.1.143

References

  1. UniProt :accession Q10469
  2. GeneReviews http://www.ncbi.nlm.nih.gov/sites/genetests/lab/gene/MGAT2
  3. GGDB; Note: glycogene database http://riodb.ibase.aist.go.jp/rcmg/ggdb/
  4. Functional glycomics gateway - GTase alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyl- transferase http://www.functionalglycomics.org/glycomics/molecule/jsp/glycoEnzyme/viewglycoEnzyme.jsp?gbpId=gt_hum_534