|
+ |
|
→ |
|
+ | 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-103a-2-5p |
---|
miRNA Target | Site Type | Pos. | Context Score | Frac. | Wt. Context | Frac. | Conserved | Quality |
---|---|---|---|---|---|---|---|---|
5'... GUGGUGGCACUGUU
UGGUCUGA
... 3' GUUCCGUCGUGACAU UUCUUCG A |
8mer | 1221-1228 | -0.253 | 95.0 | -0.253 | 96.0 | noncon | |
5'... GCGUGUCUCAGGUA
CUGCAUA
G... 3' GUUCCGUCGUGACAUU UCUUCG A |
7mer-A1 | 1282-1288 | -0.128 | 83.0 | -0.128 | 88.0 | noncon | |
5'... GGUUGGGGGCAAAG
GAGAUCA
C... 3' GUUCCGUCGUGACAUU UCUUCG A |
7mer-A1 | 1569-1575 | -0.02 | 33.0 | -0.02 | 52.0 | noncon |