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Ligand ubiquinol-0

Basic Ligand Information

Molecular Structure

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Roles as Enzyme Ligand

In Vivo Product in Enzyme-catalyzed Reactions (1 result)

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Show Natural Product (1 entry)

EC NUMBER

PROVEN IN VIVO REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.1.5.3

sn-glycerol 3-phosphate + coenzyme Q0 = dihydroxyacetone phosphate + reduced coenzyme Q0

0

-

Substrate in Enzyme-catalyzed Reactions (2 results)

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Show Substrate (2 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.10.5.1

nicotinamide riboside + reduced coenzyme Q0 = dihydronicotinamide riboside + coenzyme Q0

711729

-

7.1.1.7

2 2,3-dimethoxy-5-methyl-1,4-benzoquinol + O2 + 4 H+[side 1] = 2 2,3-dimethoxy-5-methyl-1,4-benzoquinone + 2 H2O + 4 H+[side 2]

727727

-

Product in Enzyme-catalyzed Reactions (30 results)

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Show Product (30 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

1.1.5.14

D-fructose + 2,3-dimethoxy-5-methyl-1,4-benzoquinone = 5-dehydro-D-fructose + 2,3-dimethoxy-5-methyl-1,4-benzoquinol

0

-

1.1.5.3

sn-glycerol 3-phosphate + coenzyme Q0 = dihydroxyacetone phosphate + reduced coenzyme Q0

0

-

1.1.5.3

sn-glycerol 3-phosphate + coenzyme Q0 = glycerone phosphate + reduced coenzyme Q0

0

-

1.1.5.3

2 entries

1.1.5.4

(S)-malate + ubiquinone-0 = oxaloacetate + ubiquinol-0

0

-

1.1.98.4

2,3-dimethoxy-5-methyl-1,4-benzoquinone + reduced coenzyme F420 = 2,3-dimethoxy-5-methyl-1,4-benzoquinol + oxidized coenzyme F420

0

-

1.14.18.3

propylene + coenzyme Q0 + O2 = propylene oxide + reduced coenzyme Q0 + H2O

0

-

1.17.5.2

caffeine + ubiquinone-0 = trimethyl uric acid + ubiquinol-0

0

-

1.17.5.2

theobromine + ubiquinone-0 = ? + ubiquinol-0

0

-

1.17.5.2

theophylline + ubiquinone-0 = ? + ubiquinol-0

0

-

1.17.5.2

3 entries

1.3.5.1

succinate + 2,3-dimethoxy-5-methyl-1,4-benzoquinone = fumarate + 2,3-dimethoxy-5-methyl-1,4-benzohydroquinone

391104

-

1.3.5.2

(S)-dihydroorotate + 2,3-dimethoxy-5-methyl-1,4-benzoquinone = orotate + 2,3-dimethoxy-5-methyl-1,4-benzoquinol

0

-

1.3.5.2

(S)-dihydroorotate + coenzyme Q0 = orotate + reduced coenzyme Q0

0

-

1.3.5.2

dihydroorotate + coenzyme Q0 = orotate + reduced coenzyme Q0

0

-

1.3.5.2

dihydroorotate + ubiquinone-0 = orotate + reduced ubiquinone-0

0

-

1.3.5.2

L-dihydroorotate + ubiquinone-0 = orotate + reduced ubiquinone-0

0

-

1.3.5.2

5 entries

1.5.99.12

N6-(2-isopentenyl)adenine + 2,3-dimethoxy-5-methyl-1,4-benzoquinone + H2O = adenine + 3-methylbut-2-enal + 2,3-dimethoxy-5-methyl-1,4-benzoquinol

0

-

1.6.5.10

2,3-dimethoxy-5-methyl-1,4-benzoquinone + NADPH + H+ = 2,3-dimethoxy-5-methyl-1,4-benzoquinol + NADP+

0

-

1.6.5.10

NADH + H+ + coenzyme Q0 = NAD+ + reduced coenzyme Q0

0

-

1.6.5.10

NADPH + H+ + coenzyme Q0 = NADP+ + reduced coenzyme Q0

0

-

1.6.5.10

ubiquinone-0 + NADPH + H+ = ubiquinol-0 + NADP+

0

-

1.6.5.2

deamino-NADH + H+ + 2,3-dimethoxy-5-methyl-1,4-benzoquinone = deamino-NAD+ + 2,3-dimethoxy-5-methyl-1,4-benzoquinol

0

-

1.6.5.2

NADH + H+ + 2,3-dimethoxy-5-methyl-1,4-benzoquinone = NAD+ + 2,3-dimethoxy-5-methyl-1,4-benzoquinol

0

-

1.6.5.2

NADPH + H+ + 2,3-dimethoxy-5-methyl-1,4-benzoquinone = NADP+ + 2,3-dimethoxy-5-methyl-1,4-benzoquinol

0

-

1.6.5.2

NADH + H+ + 2,3-dimethoxy-5-methyl-2,5-cyclohexadiene-1,4-dione = NAD+ + 2,3-dimethoxy-5-methylbenzene-1,4-diol

0

-

1.6.5.2

coenzyme Q0 + NAD(P)H = reduced coenzyme Q0 + NADP+

0

-

1.6.5.2

NADH + H+ + coenzyme Q0 = NAD+ + reduced coenzyme Q0

0

-

1.6.5.2

NADH + H+ + ubiquinone-0 = NAD+ + ubiquinol-0

0

-

1.6.5.10

4 entries

1.6.5.2

7 entries

1.6.5.5

2,3-dimethoxy-5-methyl-1,4-benzoquinone + NADPH + H+ = 2,3-dimethoxy-5-methyl-1,4-benzoquinol + NADP+

0

-

7.1.1.2

NADH + H+ + ubiquinone-0 = NAD+ + ubiquinol-0

0

-

7.1.1.2

NADH + ubiquinone-0 = NAD+ + ubiquinol-0

0

-

7.1.1.2

2 entries

Enzyme Cofactor/Cosubstrate (1 result)

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EC NUMBER

COMMENTARY

LITERATURE

ENZYME 3D STRUCTURE

7.1.1.8

-

440001

-

Enzyme Kinetic Parameters

References & Links

Literature References (4)

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Show Reference (4 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

391104

3511050

Reconstitution of quinone reduction and characterization of Escherichia coli fumarate reductase activity

1986

Cecchini, G.; Ackrell, B.A.C.; Deshler, J.O.; Gunsalus, R.P.

J. Biol. Chem.

261

1808-1814

440001

3036822

Identification of a stable ubisemiquinone and characterization of the effects of ubiquinone oxidation-reduction status on the Rieske iron-sulfur protein in the three-subunit ubiquinol-cytochrome c oxidoreductase complex of Paracoccus denitrificans

1987

Meinhardt, S.W.; Yang, X.; Trumpower, B.L.; Ohnishi, T.

J. Biol. Chem.

262

8702-8706

711729

20399199

Old and new inhibitors of quinone reductase 2

2010

Ferry, G.; Hecht, S.; Berger, S.; Moulharat, N.; Coge, F.; Guillaumet, G.; Leclerc, V.; Yous, S.; Delagrange, P.; Boutin, J.A.

Chem. Biol. Interact.

186

103-109

727727

8626304

Purification of a cytochrome bd terminal oxidase encoded by the Escherichia coli app locus from a delta cyo delta cyd strain complemented by genes from Bacillus firmus OF4

1996

Sturr, M.G.; Krulwich, T.A.; Hicks, D.B.

J. Bacteriol.

178

1742-1749

Links to other databases for ubiquinol-0

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ChEBI

PubChem