ALG12 transfers Man to N-glycan precursor (GlcNAc)2 (Man)7 (PP-Dol)1

Stable Identifier
R-HSA-446198
Type
Reaction
Species
Homo sapiens
Compartment
Synonyms
Addition of the eighth mannose to the N-glycan precursor by ALG12
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The eighth mannose is added to the N-glycan precursor. This reaction occurs in the ER lumen and uses dolichyl phosphate D-mannose as a mannose donor. Defects in ALG12 are the cause of congenital disorder of glycosylation type 1G (CDG1G) (Chantret I et al, 2002).

Literature References
PubMed ID Title Journal Year
11983712 Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase

Dupré, T, Danos, O, Chantret, I, Bader-Meunier, B, Seta, N, Bucher, S, Barnier, A, Heron, D, Durand, G, Codogno, P, Oriol, R, Moore, SE, Delenda, C, Charollais, A, Dancourt, J

J Biol Chem 2002
Participants
Participates
Catalyst Activity

mannosyltransferase activity of ALG12 [endoplasmic reticulum membrane]

This event is regulated
Orthologous Events
Authored
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Created
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