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Literature summary for 2.7.11.14 extracted from
- Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness (1997), Nat. Genet., 15, 175-178.
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| ATP + rhodopsin | Homo sapiens | null mutations in the rhodopsin kinase gene are a cause of Oguchi disease and extend the known genetic heterogeneity in congenital stationary night blindness | ADP + phosphorylated rhodopsin | - |
? |  |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | Q15835 | - |
- |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| ATP + rhodopsin | - |
Homo sapiens | ADP + phosphorylated rhodopsin | - |
? | |
| ATP + rhodopsin | null mutations in the rhodopsin kinase gene are a cause of Oguchi disease and extend the known genetic heterogeneity in congenital stationary night blindness | Homo sapiens | ADP + phosphorylated rhodopsin | - |
? | |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| rhodopsin kinase | - |
Homo sapiens |
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Release 2023.1 (January 2023)
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