dolichyl pyrophosphate man9GlcNAc2 alpha-1,3-glucosyltransferase; asparagine-linked glycosylation protein 6 homolog; dol-P-Glc:man(9)GlcNAc(2)-PP-dol alpha-1,3-glucosyltransferase; dolichyl-P-Glc:man9GlcNAc2-PP-dolichyl glucosyltransferase (ALG6)
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Function
- adds the first glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation
- transfers glucose from dolichyl phosphate glucose (dol-P-Glc) onto the lipid-linked oligosaccharide man(9)GlcNAc(2)-PP-dol
- protein modification; protein glycosylation
Structure
belongs to the ALG6/ALG8 glucosyltransferase family
Compartment
- endoplasmic reticulum membrane
- multi-pass membrane protein (putative)
Pathology
- defects in ALG6 are the cause of congenital disorder of glycosylation type 1C
More general terms
Additional terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/Q9Y672.html
- ↑ GeneReviews http://www.ncbi.nlm.nih.gov/sites/genetests/lab/gene/ALG6
- ↑ GGDB; Note: glycogene database http://riodb.ibase.aist.go.jp/rcmg/ggdb/