EC Number |
Inhibitors |
Structure |
---|
2.7.3.2 | NO3- |
- |
|
2.7.3.2 | p-hydroxymercuribenzoate |
- |
|
2.7.3.2 | Pb2+ |
lead inhibits in vitro the cytosolic and mitochondrial creatine kinase activity at 0.2 mM and that this inhibition is prevented by addition cysteamine to the assay at 0.1 mM and 0.5 mM final concentration |
|
2.7.3.2 | Phenylglyoxal |
complete inactivation, reacts on arginine residues |
|
2.7.3.2 | phosphate |
competitive against ATP and phosphocreatine, noncompetitive against ADP and creatine |
|
2.7.3.2 | Pipes buffer |
i.e. 1,4-piperazine diethanesulfonic acid |
|
2.7.3.2 | quercetin |
mechanism, role of radicals |
|
2.7.3.2 | SDS |
dissociation of subunits, no unfolding |
|
2.7.3.2 | SDS |
strongly inhibits the CK-BB activity in a noncompetitive manner, although almost all the activity is eliminated by SDS CK-BB is never completely inactivated (4% to 5% activity is still sustained), regardless of increased incubation time or SDS concentration |
|
2.7.3.2 | SO32- |
- |
|