Primary Identifier | IPR039485 | Type | Family |
Short Name | ALG12 |
description | N-linked glycosylation in eukaryotes requires the assembly of lipid-linkedoligosaccharide (LLO) precursor Glc3Man9GlcNAc2-pyrophosphate-dolichol (Glc3Man9Gn2-PDol). Addition of sugars to LLO is carried out sequentially by a serie of asparagine-linked glycosylation (Alg) glycosyltransferases []. ALG12 adds the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man7GlcNAc2). Deficiency of ALG12 results in glycosylation disorder type lG [, ]. |