Putidaredoxin (PdX), the physiological effector of cytochrome P450cam (P450cam), serves to gate electron transfer into oxy- P450cam during the catalytic cycle of the enzyme. Redox-linked structural changes in PdX are necessary for the effective P450cam turnover reaction. PdX is believed to be difficult to be replaced by an artificial electron donor in the reaction pathway of P450cam. We demonstrate that the catalytic cycle of wild-type P450cam can be supported in the presence of an artificial reductant, potassium ferrocyanide. Upon rapid mixing of ferrocyanide ion with P450cam, we observed an intermediate with spectral features characteristic of compound I. The rate constant for the formation of compound I in the presence of ferrocyanide sup...
Cytochromes P450 contain a heme center where the activation of molecular oxygen occurs, resulting in...
The strict requirement of cytochrome P450cam for its native ferredoxin redox partner, putidaredoxin ...
Camphor is hydroxylated in the soil bacterium Pseudomonas putida by a soluble three protein monoxyge...
Putidaredoxin (PdX), the physiological effector of cytochrome P450cam (P450cam), serves to gate elec...
The most recognized activity of P450cam is the oxidation of the unactivated C-H bond at C-5 of D (+)...
[[abstract]]Cytochrome P450(cam) (CYP101) catalyzes the oxidation of D(+)-camphor at the 5 position....
AbstractCytochrome P450cam catalyzes the hydroxylation of camphor in a complex process involving two...
Cytochrome P450cam is an archetypal example of the vast family of heme monooxygenases and serves as ...
[[abstract]]Cytochrome P450(cam) (CYP101) catalyzes the oxidation of D(+)-camphor at the 5 position....
Cytochrome P450cam is an archetypal example of the vast family of heme monooxygenases and serves as ...
Cytochrome P450 CYP101A1 (P450cam) hydroxylates camphor by receiving two distinct electrons from its...
Cytochrome P450 (CYP) enzymes of the CYP101 and CYP111 families from the oligotrophic bacterium Novo...
AbstractIn anaerobic environments the first electron transfer in substrate-free P450cam is known to ...
The cytochrome P-450$\sb{\rm cam}$ reaction cycle is a complex set of coordinated chemical transform...
Cytochrome P450 (CYP) enzymes of the CYP101 and CYP111 families from the oligotrophic bacterium Novo...
Cytochromes P450 contain a heme center where the activation of molecular oxygen occurs, resulting in...
The strict requirement of cytochrome P450cam for its native ferredoxin redox partner, putidaredoxin ...
Camphor is hydroxylated in the soil bacterium Pseudomonas putida by a soluble three protein monoxyge...
Putidaredoxin (PdX), the physiological effector of cytochrome P450cam (P450cam), serves to gate elec...
The most recognized activity of P450cam is the oxidation of the unactivated C-H bond at C-5 of D (+)...
[[abstract]]Cytochrome P450(cam) (CYP101) catalyzes the oxidation of D(+)-camphor at the 5 position....
AbstractCytochrome P450cam catalyzes the hydroxylation of camphor in a complex process involving two...
Cytochrome P450cam is an archetypal example of the vast family of heme monooxygenases and serves as ...
[[abstract]]Cytochrome P450(cam) (CYP101) catalyzes the oxidation of D(+)-camphor at the 5 position....
Cytochrome P450cam is an archetypal example of the vast family of heme monooxygenases and serves as ...
Cytochrome P450 CYP101A1 (P450cam) hydroxylates camphor by receiving two distinct electrons from its...
Cytochrome P450 (CYP) enzymes of the CYP101 and CYP111 families from the oligotrophic bacterium Novo...
AbstractIn anaerobic environments the first electron transfer in substrate-free P450cam is known to ...
The cytochrome P-450$\sb{\rm cam}$ reaction cycle is a complex set of coordinated chemical transform...
Cytochrome P450 (CYP) enzymes of the CYP101 and CYP111 families from the oligotrophic bacterium Novo...
Cytochromes P450 contain a heme center where the activation of molecular oxygen occurs, resulting in...
The strict requirement of cytochrome P450cam for its native ferredoxin redox partner, putidaredoxin ...
Camphor is hydroxylated in the soil bacterium Pseudomonas putida by a soluble three protein monoxyge...