EC Number   |
Natural Substrates |
|---|
   7.2.1.1 | deamino-NADH + H+ + ubiquinone + 2 Na+/in |
- |
| 7.2.1.1 | deamino-NADH + H+ + ubiquinone + n Na+/in |
- |
| 7.2.1.1 | more |
the enzyme is the entry point for electrons into the respiratory chain |
| 7.2.1.1 | more |
construction of a double NDH-2/NDH-1-deficient strain. Sub-bacterial particles isolated from these strains oxidize NADH entirely via the corresponding Na+-NQR, which makes them a useful tool to study the catalytic properties of these enzymes |
| 7.2.1.1 | more |
construction of a NADH-dehydrogenase NDH-2-deficient strain. Sub-bacterial particles isolated from these strains oxidize NADH entirely via the corresponding Na+-NQR, which makes them a useful tool to study the catalytic properties of these enzymes |
| 7.2.1.1 | more |
in addition to the quinone reductase reaction the isolated enzyme can also catalyze so-called NADH dehydrogenase reaction during interaction with soluble quinines. This activity includes a single-electron reduction of soluble quinones (menadione, Q0, Q1, etc.) or some other electron acceptors (hexammineruthenium(III), ferricyanide, etc.). Similarly to the transdehydrogenase activity, the NADH dehydrogenase activity does not depend on concentration of sodium ions, is inhibited by heavy metal ions, and is insensitive to 2-heptyl-4-hydroxyquinoline N-oxide and korormicin |
| 7.2.1.1 | more |
in addition to the quinone reductase reaction the isolated enzyme can also catalyze so-called NADH dehydrogenase reaction during interaction with soluble quinones. This activity includes a single-electron reduction of soluble quinones (menadione, Q0, Q1, etc.) or some other electron acceptors (hexammineruthenium(III), ferricyanide, etc.). Similarly to the transdehydrogenase activity, the NADH dehydrogenase activity does not depend on concentration of sodium ions, is inhibited by heavy metal ions, and insensitive to 2-heptyl-4-hydroxyquinoline N-oxide and korormicin |
| 7.2.1.1 | more |
in addition to the quinone reductase reaction the isolated enzyme can also catalyze so-called NADH dehydrogenase reaction during interaction with soluble quinones. This activity includes a single-electron reduction of soluble quinones (menadione, Q0, Q1, etc.) or some other electron acceptors (hexammineruthenium(III), ferricyanide, etc.). Similarly to the transdehydrogenase activity, the NADH dehydrogenase activity does not depend on concentration of sodium ions, is inhibited by heavy metal ions, and is insensitive to 2-heptyl-4-hydroxyquinoline N-oxide and korormicin |
| 7.2.1.1 | more |
in addition to the quinone reductase reaction, the isolated enzyme can also catalyze the so-called NADH-dehydrogenase reaction during interaction with soluble quinones. This activity includes a single-electron reduction of soluble quinones (menadione, Q0, Q1, etc.) or some other electron acceptors (hexaammineruthenium (III), ferricyanide, etc.) |
| 7.2.1.1 | more |
Na+-NQR does not oxidize NADPH |
