|
+ |
|
→ |
|
+ | 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-4673 |
---|
miRNA Target | Site Type | Pos. | Context Score | Frac. | Wt. Context | Frac. | Conserved | Quality |
---|---|---|---|---|---|---|---|---|
5'...CCUAUCCCUGGGCU
CCCCAGGA
... 3' AGGUCAGGCCGAGG ACGGACC U |
8mer | 938-945 | -0.265 | 97.0 | -0.265 | 98.0 | noncon | |
5'...CCUGAGCCAAUCCA
UCCACCU
A... 3' AGGUCAGGCCGAGGA CGGACC U |
6mer | 2010-2016 | -0.132 | 87.0 | -0.132 | 91.0 | noncon | |
5'...AACAGUUUUCAUUG
ACGGCUA
C... 3' AGGUCAGGCCGAGGA CGGACC U |
7mer-A1 | 1006-1012 | -0.113 | 83.0 | -0.113 | 89.0 | noncon |