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

Stable Identifier
R-HSA-446198
Type
Reaction [transition]
Species
Homo sapiens
Compartment
Synonyms
Addition of the eighth mannose to the N-glycan precursor by ALG12
ReviewStatus
5/5
Locations in the PathwayBrowser
General
SVG |   | PPTX  | SBGN
Click the image above or here to open this reaction in the Pathway Browser
The layout of this reaction may differ from that in the pathway view due to the constraints in pathway layout
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
Reviewed
Created
Cite Us!