1.1.1.379: (R)-mandelate dehydrogenase
This is an abbreviated version!
For detailed information about (R)-mandelate dehydrogenase, go to the full flat file.
Word Map on EC 1.1.1.379
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1.1.1.379
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dehydrogenases
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enterococcus
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acinetobacter
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2-ketoacids
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calcoaceticus
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faecalis
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rhodotorula
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benzoylformate
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d-2-hydroxyacid
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phenylglyoxylic
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enantiomer
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graminis
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l+-lactate
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dye-linked
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synthesis
- 1.1.1.379
- dehydrogenases
-
enterococcus
-
acinetobacter
-
2-ketoacids
- calcoaceticus
-
faecalis
- rhodotorula
- benzoylformate
- d-2-hydroxyacid
-
phenylglyoxylic
-
enantiomer
- graminis
-
l+-lactate
-
dye-linked
- synthesis
Reaction
Synonyms
D(-)-mandelate dehydrogenase, D-mandelate dehydrogenase, D-ManDH, D-ManDH2, DMDH, LhDMDH, ManDH2, NAD+-dependent D-mandelate dehydrogenase, NAD-dependent D-mandelate dehydrogenase
ECTree
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Inhibitors
Inhibitors on EC 1.1.1.379 - (R)-mandelate dehydrogenase
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(2R)-[(bromoacetyl)oxy]mandelic acid
8 mM, greater than 95% inactivation after 2 h at 27°C. Inactivation is a pseudo-first-order process. D-Mandelate protects against inactivation. The inhibitor is covalently bound
additional information
neither stimulated nor inhibited by 1 mM concentrations of NaCl, Na2SO4, KCl, MgCl2, NH4Cl, CaCl2, ZnCl2, CoCl2, FeCl3, KH2PO4, NaH2PO4, MnSO4, MnCl2 or CuSO4. Not inhibited by the following metal-chelating agents each at 1 mM: EDTA, diethyldithiocarbamic acid, bathophenanthroline disulfonic acid, dihydroxybenzene disulfonic acid, pyrazole, 8-hydroxyquinoline or 2,2'-dipyridyl. Little or no inhibition of enzyme activity by 10 mM iodoacetate, 10 mM iodoacetamide, 6.65 mM 5,5'-dithiobis(2-nitrobenzoic acid) or 5 mM 4-chloromercuribenzoate, even after a 6 h preincubation at 27°C. Neither inhibited nor stimulated by 1 mM concentrations of benzaldehyde, benzoate, succinate, glucose, ATP/Mg2+, ADP/Mg2+ or acetyl-CoA
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