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Literature summary for 2.4.1.255 extracted from
- Synthesis of a benzene-containing C1-phosphonate analogue of UDP-GlcNAc for the inhibition of O-GlcNAc transferase (2016), Bull. Korean Chem. Soc., 37, 7-12.
No PubMed abstract available
Inhibitors
| Inhibitors | Comment | Organism | Structure |
|---|---|---|---|
| uridine 5'-[[(2-acetylamino-5-hydroxymethyl-benzyl)-phosphono]phosphate] | designed to mimic the transition state of the natural donor involved in the enzymatic reaction. The analogue shows low activity as an inhibitor | Homo sapiens |  |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | - |
- |
- |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| casein kinase II + UDP-GlcNAc | - |
Homo sapiens | ? + UDP | - |
? | |
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