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Ligand (4R)-dihydrocarvone Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Basic Ligand Information Molecular Structure
C1 0 H1 6 O
(4R)-dihydrocarvone
AZOCECCLWFDTAP-RKDXNWHRSA-N
(+)-dihydrocarvone, (1R,4R)-dihydrocarvone, (2R,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one
Roles as Enzyme Ligand
Substrate in Enzyme-catalyzed Reactions (2 results)
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(1R,4R)-dihydrocarvone + NADPH + H+ + O2 = (4R,7R)-4-isopropenyl-7-methyl-2-oxo-oxepanone + NADP+ + H2O
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(+)-dihydrocarvone + NADPH + O2 = ?
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Product in Enzyme-catalyzed Reactions (3 results)
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(1R,2R,4R)-dihydrocarveol + NAD+ = (1R,4R)-dihydrocarvone + NADH + H+
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(1R,2S,4R)-neo-dihydrocarveol + NAD+ = (1R,4R)-dihydrocarvone + NADH + H+
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(5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one + NADH + H+ = (2R,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one + NAD+
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Enzyme Kinetic Parameters
kcat Value (Turnover Number) (1 result)
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3.9
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30°C and glyine/NaOH buffer, pH 9.5
KM Value (1 result)
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0.13
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30°C and glyine/NaOH buffer, pH 9.5
References & Links Literature References (3)
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Enzymatic Baeyer-Villiger type oxidations of ketones catalyzed by cyclohexanone oxygenase
1989
Abril, O.; Ryerson, C.C.; Walsh, C.; Whitesides, G.M.
Bioorg. Chem.
17
41-52
The purification and properties of cyclohexanone oxygenase from Nocardia globerula CL1 and Acinetobacter NCIB 9871
1976
Donoghue, N.A.; Norris, D.B.; Trudgill, P.W.
Eur. J. Biochem.
63
175-192
Purification and characterization of a Baeyer-Villiger mono-oxygenase from Rhodococcus erythropolis DCL14 involved in three different monocyclic monoterpene degradation pathways
2000
van der Werf, M.J.
Biochem. J.
347 Pt 3
693-701
Links to other databases for (4R)-dihydrocarvone