EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
2.7.8.15 | Y170C | mutant enzyme has almost no activity | Homo sapiens |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.8.15 | UDP-N-acetyl-D-glucosamine + dolichyl phosphate | Homo sapiens | deficiency of UDP-GlcNAc:dolichol phosphate N-acetylglucosamine-1 phosphate transferase (DPAGT1) causes a novel congenital disorder of glycosylation type Ij | ? | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.7.8.15 | Homo sapiens | - |
- |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.7.8.15 | UDP-N-acetyl-alpha-D-glucosamine + dolichyl phosphate | - |
Homo sapiens | UMP + N-acetyl-alpha-D-glucosaminyl-diphosphodolichol | - |
? | |
2.7.8.15 | UDP-N-acetyl-D-glucosamine + dolichyl phosphate | deficiency of UDP-GlcNAc:dolichol phosphate N-acetylglucosamine-1 phosphate transferase (DPAGT1) causes a novel congenital disorder of glycosylation type Ij | Homo sapiens | ? | - |
? |