Activating Compound | Comment | Organism | Structure |
---|---|---|---|
BAY 60-2770 | activator BAY 60-2770 has higher efficiency on the purified protein than BAY 58-2667, i.e. cinaciguat | Homo sapiens | |
cinaciguat | i.e. BAY 58-2667. Activator BAY 60-2770 has higher efficiency on the purified protein than BAY 58-2667 | Homo sapiens |
Cloned (Comment) | Organism |
---|---|
transfection of Sf9 cells | Homo sapiens |
Protein Variants | Comment | Organism |
---|---|---|
D530A | mutation in alpha subunit. Protein levels of the catalytically inactive, non-nucleotide binding mutant a1/b1 are not affected by activator drugs | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
GTP | - |
Homo sapiens | 3',5'-cGMP + diphosphate | - |
? |
General Information | Comment | Organism |
---|---|---|
physiological function | in the presence of activators BAY 58-2667 (cinaciguat) and BAY 60-2770, protein levels of isoforms alpha1/beta1 and alpha2/beta1 overexpressed in Sf9 cells decrease. The activator drugs stably insert into the enzyme during protein biosynthesis independent of the heme redox state | Homo sapiens |