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  Domain Name: ALG3
ALG3 protein. The formation of N-glycosidic linkages of glycoproteins involves the ordered assembly of the common Glc3Man9GlcNAc2 core-oligosaccharide on the lipid carrier dolichyl pyrophosphate. Whereas early mannosylation steps occur on the cytoplasmic side of the endoplasmic reticulum with GDP-Man as donor, the final reactions from Man5GlcNAc2-PP-Dol to Man9GlcNAc2-PP-Dol on the lumenal side use Dol-P-Man. ALG3 gene encodes the Dol-P-Man:Man5GlcNAc2-PP-Dol mannosyltransferase.
No pairwise interactions found for the domain ALG3

Total Mutations Found: 10
Total Disease Mutations Found: 8
This domain occurred 1 times on human genes (3 proteins).



  CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID


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   Protein ID            Protein Position

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No Conserved Features/Sites Found for ALG3

















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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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