|
+ |
|
→ |
|
+ | UDP |
* O-mannosyl glycans are a type of O-glycan in which the reducing terminal mannose is attached to Ser/Thr.
* POMGnT1 catalyzes the transfer of β1,2GlcNAc from UDP-GlcNAc to O-mannose of glycoproteins.
* POMGnT1 deficiency results in muscle-eye-brain disease (MEB), a form of congenital muscular dystrophy/ a-dystroglycanopathy.
* POMGnT1 cannot recognize 6P-Man-peptide as an acceptor. Thus O-mannose phosphorylation occurs after the formation of GlcNAcβ1-2Man linkage.
ER | Cis- | Medial- | Trans- | TGN |
---|---|---|---|---|
POMGNT1/hsa-miR-1200 |
---|
miRNA Target | Site Type | Pos. | Context Score | Frac. | Wt. Context | Frac. | Conserved | Quality |
---|---|---|---|---|---|---|---|---|
5'...UGCCUGGAAUGACC
AGGUAGGC
... 3' CUCCGAGUCUUACC GAGUCCU C |
8mer | 2064-2071 | -0.258 | 96.0 | -0.258 | 97.0 | noncon | |
5'...ACUCCCAUCAGCAU
CAAGAAUG
... 3' CUCCGAGUCUUACC GAGUCCU C |
8mer | 1257-1264 | -0.135 | 84.0 | -0.135 | 89.0 | noncon | |
5'...ACUAUGAGGUGAGC
AGGACUU
G... 3' CUCCGAGUCUUACCG AGUCCU C |
6mer | 1026-1032 | -0.02 | 39.0 | -0.02 | 60.0 | noncon |