Application | Comment | Organism |
---|---|---|
medicine | Vibrio cholerae Na+-NQR is significant for the induction of virulence factors. Thus, this enzyme can be used as a target in the treatment or prevention of many infectious diseases | Vibrio cholerae serotype O1 |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
2-heptyl-4-hydroxyquinoline N-oxide | - |
Haemophilus influenzae | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Klebsiella pneumoniae | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Neisseria gonorrhoeae | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Neisseria meningitidis | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Porphyromonas gingivalis | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Pseudomonas aeruginosa | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Shewanella putrefaciens | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Vibrio alginolyticus | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Vibrio cholerae serotype O1 | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Vibrio harveyi | |
2-heptyl-4-hydroxyquinoline N-oxide | - |
Yersinia pestis | |
korormicin | - |
Haemophilus influenzae | |
korormicin | - |
Klebsiella pneumoniae | |
korormicin | - |
Neisseria gonorrhoeae | |
korormicin | - |
Neisseria meningitidis | |
korormicin | - |
Porphyromonas gingivalis | |
korormicin | - |
Pseudomonas aeruginosa | |
korormicin | - |
Shewanella putrefaciens | |
korormicin | - |
Vibrio alginolyticus | |
korormicin | - |
Vibrio cholerae serotype O1 | |
korormicin | - |
Vibrio harveyi | |
korormicin | - |
Yersinia pestis |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Haemophilus influenzae | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Vibrio harveyi | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Pseudomonas aeruginosa | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Neisseria gonorrhoeae | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Neisseria meningitidis | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Klebsiella pneumoniae | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Yersinia pestis | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Porphyromonas gingivalis | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Vibrio cholerae serotype O1 | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Vibrio alginolyticus | |
Na+ | sodium ions are indispensable components of the Na+-NQR-catalyzed reaction, therefore its rate depends on concentration of Na+ and the reaction virtually does not occur in media depleted in this ion | Shewanella putrefaciens |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
21500 | - |
1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
22700 | - |
1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
27500 | - |
1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
45200 | - |
1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
45400 | - |
1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
48400 | - |
1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
additional information | Porphyromonas gingivalis | 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 | ? | - |
? | |
additional information | Vibrio harveyi | 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 | ? | - |
? | |
additional information | Vibrio alginolyticus | 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 | ? | - |
? | |
additional information | Haemophilus influenzae | 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 | ? | - |
? | |
additional information | Pseudomonas aeruginosa | 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 | ? | - |
? | |
additional information | Neisseria gonorrhoeae | 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 | ? | - |
? | |
additional information | Neisseria meningitidis | 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 | ? | - |
? | |
additional information | Klebsiella pneumoniae | 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 | ? | - |
? | |
additional information | Yersinia pestis | 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 | ? | - |
? | |
additional information | Vibrio cholerae serotype O1 | 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 | ? | - |
? | |
additional information | Shewanella putrefaciens | 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 | ? | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Haemophilus influenzae | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Vibrio harveyi | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Pseudomonas aeruginosa | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Neisseria gonorrhoeae | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Neisseria meningitidis | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Klebsiella pneumoniae | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Yersinia pestis | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Porphyromonas gingivalis | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Vibrio cholerae serotype O1 | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Vibrio alginolyticus | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | Shewanella putrefaciens | - |
NAD+ + ubiquinol + 2 Na+/out | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Haemophilus influenzae | - |
- |
- |
Klebsiella pneumoniae | - |
- |
- |
Neisseria gonorrhoeae | - |
- |
- |
Neisseria meningitidis | - |
- |
- |
Porphyromonas gingivalis | - |
- |
- |
Pseudomonas aeruginosa | - |
- |
- |
Shewanella putrefaciens | - |
- |
- |
Vibrio alginolyticus | - |
- |
- |
Vibrio cholerae serotype O1 | - |
- |
- |
Vibrio harveyi | - |
- |
- |
Yersinia pestis | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
additional information | 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 | Porphyromonas gingivalis | ? | - |
? | |
additional information | 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 | Vibrio harveyi | ? | - |
? | |
additional information | 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 | Vibrio alginolyticus | ? | - |
? | |
additional information | 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 | Haemophilus influenzae | ? | - |
? | |
additional information | 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 | Pseudomonas aeruginosa | ? | - |
? | |
additional information | 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 | Neisseria gonorrhoeae | ? | - |
? | |
additional information | 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 | Neisseria meningitidis | ? | - |
? | |
additional information | 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 | Klebsiella pneumoniae | ? | - |
? | |
additional information | 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 | Yersinia pestis | ? | - |
? | |
additional information | 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 | Vibrio cholerae serotype O1 | ? | - |
? | |
additional information | 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 | Shewanella putrefaciens | ? | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Haemophilus influenzae | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Vibrio harveyi | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Pseudomonas aeruginosa | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Neisseria gonorrhoeae | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Neisseria meningitidis | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Klebsiella pneumoniae | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Yersinia pestis | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Porphyromonas gingivalis | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Vibrio cholerae serotype O1 | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Vibrio alginolyticus | NAD+ + ubiquinol + 2 Na+/out | - |
? | |
NADH + H+ + ubiquinone + 2 Na+/in | - |
Shewanella putrefaciens | NAD+ + ubiquinol + 2 Na+/out | - |
? |
Subunits | Comment | Organism |
---|---|---|
heterohexamer | - |
Haemophilus influenzae |
heterohexamer | - |
Pseudomonas aeruginosa |
heterohexamer | - |
Neisseria gonorrhoeae |
heterohexamer | - |
Neisseria meningitidis |
heterohexamer | - |
Klebsiella pneumoniae |
heterohexamer | - |
Yersinia pestis |
heterohexamer | - |
Porphyromonas gingivalis |
heterohexamer | - |
Vibrio cholerae serotype O1 |
heterohexamer | - |
Vibrio alginolyticus |
heterohexamer | - |
Shewanella putrefaciens |
heterohexamer | 1 * 48400 + 1 * 45400 + 1 * 27500 + 1 * 22700 + 1 * 21500 + 1 * 45200 | Vibrio harveyi |
Synonyms | Comment | Organism |
---|---|---|
Na+-NQR | - |
Haemophilus influenzae |
Na+-NQR | - |
Vibrio harveyi |
Na+-NQR | - |
Pseudomonas aeruginosa |
Na+-NQR | - |
Neisseria gonorrhoeae |
Na+-NQR | - |
Neisseria meningitidis |
Na+-NQR | - |
Klebsiella pneumoniae |
Na+-NQR | - |
Yersinia pestis |
Na+-NQR | - |
Porphyromonas gingivalis |
Na+-NQR | - |
Vibrio cholerae serotype O1 |
Na+-NQR | - |
Vibrio alginolyticus |
Na+-NQR | - |
Shewanella putrefaciens |
Na+-translocating NADH:quinone oxidoreductase | - |
Haemophilus influenzae |
Na+-translocating NADH:quinone oxidoreductase | - |
Vibrio harveyi |
Na+-translocating NADH:quinone oxidoreductase | - |
Pseudomonas aeruginosa |
Na+-translocating NADH:quinone oxidoreductase | - |
Neisseria gonorrhoeae |
Na+-translocating NADH:quinone oxidoreductase | - |
Neisseria meningitidis |
Na+-translocating NADH:quinone oxidoreductase | - |
Klebsiella pneumoniae |
Na+-translocating NADH:quinone oxidoreductase | - |
Yersinia pestis |
Na+-translocating NADH:quinone oxidoreductase | - |
Porphyromonas gingivalis |
Na+-translocating NADH:quinone oxidoreductase | - |
Vibrio cholerae serotype O1 |
Na+-translocating NADH:quinone oxidoreductase | - |
Vibrio alginolyticus |
Na+-translocating NADH:quinone oxidoreductase | - |
Shewanella putrefaciens |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
FAD | noncovalently bound to subunit NqrF | Haemophilus influenzae | |
FAD | noncovalently bound to subunit NqrF | Vibrio harveyi | |
FAD | noncovalently bound to subunit NqrF | Pseudomonas aeruginosa | |
FAD | noncovalently bound to subunit NqrF | Neisseria gonorrhoeae | |
FAD | noncovalently bound to subunit NqrF | Neisseria meningitidis | |
FAD | noncovalently bound to subunit NqrF | Klebsiella pneumoniae | |
FAD | noncovalently bound to subunit NqrF | Yersinia pestis | |
FAD | noncovalently bound to subunit NqrF | Porphyromonas gingivalis | |
FAD | noncovalently bound to subunit NqrF | Vibrio cholerae serotype O1 | |
FAD | noncovalently bound to subunit NqrF | Vibrio alginolyticus | |
FAD | noncovalently bound to subunit NqrF | Shewanella putrefaciens | |
FMN | covalently bound to subunits NqrB and NqrC | Haemophilus influenzae | |
FMN | covalently bound to subunits NqrB and NqrC | Vibrio harveyi | |
FMN | covalently bound to subunits NqrB and NqrC | Pseudomonas aeruginosa | |
FMN | covalently bound to subunits NqrB and NqrC | Neisseria gonorrhoeae | |
FMN | covalently bound to subunits NqrB and NqrC | Neisseria meningitidis | |
FMN | covalently bound to subunits NqrB and NqrC | Klebsiella pneumoniae | |
FMN | covalently bound to subunits NqrB and NqrC | Yersinia pestis | |
FMN | covalently bound to subunits NqrB and NqrC | Porphyromonas gingivalis | |
FMN | covalently bound to subunits NqrB and NqrC | Vibrio cholerae serotype O1 | |
FMN | covalently bound to subunits NqrB and NqrC | Vibrio alginolyticus | |
FMN | covalently bound to subunits NqrB and NqrC | Shewanella putrefaciens | |
NADH | - |
Haemophilus influenzae | |
NADH | - |
Vibrio harveyi | |
NADH | - |
Pseudomonas aeruginosa | |
NADH | - |
Neisseria gonorrhoeae | |
NADH | - |
Neisseria meningitidis | |
NADH | - |
Klebsiella pneumoniae | |
NADH | - |
Yersinia pestis | |
NADH | - |
Porphyromonas gingivalis | |
NADH | - |
Vibrio cholerae serotype O1 | |
NADH | - |
Vibrio alginolyticus | |
NADH | - |
Shewanella putrefaciens | |
riboflavin | contains a noncovalently bound riboflavin | Haemophilus influenzae | |
riboflavin | contains a noncovalently bound riboflavin | Vibrio harveyi | |
riboflavin | contains a noncovalently bound riboflavin | Pseudomonas aeruginosa | |
riboflavin | contains a noncovalently bound riboflavin | Neisseria gonorrhoeae | |
riboflavin | contains a noncovalently bound riboflavin | Neisseria meningitidis | |
riboflavin | contains a noncovalently bound riboflavin | Klebsiella pneumoniae | |
riboflavin | contains a noncovalently bound riboflavin | Yersinia pestis | |
riboflavin | contains a noncovalently bound riboflavin | Porphyromonas gingivalis | |
riboflavin | contains a noncovalently bound riboflavin | Vibrio cholerae serotype O1 | |
riboflavin | contains a noncovalently bound riboflavin | Vibrio alginolyticus | |
riboflavin | contains a noncovalently bound riboflavin | Shewanella putrefaciens | |
ubiquinone-8 | - |
Haemophilus influenzae | |
ubiquinone-8 | - |
Vibrio harveyi | |
ubiquinone-8 | - |
Pseudomonas aeruginosa | |
ubiquinone-8 | - |
Neisseria gonorrhoeae | |
ubiquinone-8 | - |
Neisseria meningitidis | |
ubiquinone-8 | - |
Klebsiella pneumoniae | |
ubiquinone-8 | - |
Yersinia pestis | |
ubiquinone-8 | - |
Porphyromonas gingivalis | |
ubiquinone-8 | - |
Vibrio cholerae serotype O1 | |
ubiquinone-8 | - |
Vibrio alginolyticus | |
ubiquinone-8 | - |
Shewanella putrefaciens | |
[2Fe-2S]-center | part of subunit NqrF | Haemophilus influenzae | |
[2Fe-2S]-center | part of subunit NqrF | Vibrio harveyi | |
[2Fe-2S]-center | part of subunit NqrF | Pseudomonas aeruginosa | |
[2Fe-2S]-center | part of subunit NqrF | Neisseria gonorrhoeae | |
[2Fe-2S]-center | part of subunit NqrF | Neisseria meningitidis | |
[2Fe-2S]-center | part of subunit NqrF | Klebsiella pneumoniae | |
[2Fe-2S]-center | part of subunit NqrF | Yersinia pestis | |
[2Fe-2S]-center | part of subunit NqrF | Porphyromonas gingivalis | |
[2Fe-2S]-center | part of subunit NqrF | Vibrio cholerae serotype O1 | |
[2Fe-2S]-center | part of subunit NqrF | Vibrio alginolyticus | |
[2Fe-2S]-center | part of subunit NqrF | Shewanella putrefaciens |