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(R,S)-2-hydroxy-3-butenoic acid + acceptor
2-oxo-3-butenoic acid + reduced acceptor
(R,S)-2-hydroxybutyrate + acceptor
2-oxobutyrate + reduced acceptor
Substrates: slow substrate
Products: -
?
(R,S)-2-hydroxybutyric acid + acceptor
2-oxo-3-butynoic acid + reduced acceptor
Substrates: very low binding affinity for MDH
Products: -
?
(R,S)-2-hydroxyhexanoate + acceptor
2-oxohexanoate + reduced acceptor
Substrates: -
Products: -
?
(R,S)-2-hydroxyisocaproate + acceptor
2-oxoisocaproate + reduced acceptor
Substrates: -
Products: -
?
(R,S)-2-hydroxyisovalerate + acceptor
2-oxo-isovalerate + reduced acceptor
(R,S)-2-hydroxyoctanoate + acceptor
2-oxooctanoate + reduced acceptor
Substrates: slow substrate
Products: -
?
(R,S)-2-hydroxyvalerate + acceptor
2-oxovalerate + reduced acceptor
Substrates: -
Products: -
?
(R,S)-3-indolelactate + acceptor
3-(1H-indol-2-yl)-2-oxopropanoate + reduced acceptor
Substrates: -
Products: -
?
(R,S)-3-phenyllactate + 2,6-dichlorophenolindophenol
phenylpyruvate + reduced 2,6-dichlorophenolindophenol
Substrates: slow substrate
Products: -
?
(R,S)-indoleglycolate + acceptor
indol-2-yl(oxo)acetate + reduced acceptor
Substrates: -
Products: -
?
(R,S)-mandelate + 2,6-dichlorophenolindophenol
2-oxo-2-phenylacetate + reduced 2,6-dichlorophenolindophenol
Substrates: -
Products: -
?
(R,S)-mandelate + ferricyanide
2-oxo-2-phenylacetate + ferrocyanide
Substrates: -
Products: -
?
(R,S)-p-chloromandelate + acceptor
?
-
Substrates: -
Products: -
?
(S)-2-hydroxy-2-phenylacetate + O2
2-oxo-2-phenylacetate + H2O2
-
Substrates: in absence of any other electron acceptor, oxygen is used by the wild-type enzyme for reoxidation of the reduced flavin, at a rather slow rate. Ping-pong kinetics
Products: -
?
(S)-3-phenyllactate + acceptor
?
-
Substrates: -
Products: -
?
(S)-mandelate + 2 ferricyanide
2-oxo-2-phenylacetate + 2 ferrocyanide + 2 H+
(S)-mandelate + 2 ferricyanide
benzoylformic acid + 2 ferrocyanide + 2 H+
-
Substrates: -
Products: -
?
(S)-mandelate + 2,6-dichloroindophenol
2-oxo-2-phenylacetate + ?
-
Substrates: -
Products: -
?
(S)-mandelate + 2,6-dichlorophenolindophenol
2-oxo-2-phenylacetate + reduced 2,6-dichlorophenolindophenol
-
Substrates: -
Products: -
?
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
(S)-mandelate + acceptor
benzoylformate + reduced acceptor
Substrates: -
Products: -
?
(S)-mandelate + acceptor
phenylglyoxylate + reduced acceptor
Substrates: -
Products: -
?
(S)-mandelate + cytochrome c
2-oxo-2-phenylacetate + ?
-
Substrates: -
Products: -
?
(S)-mandelate + FMN
benzoylformic acid + FMNH2
-
Substrates: -
Products: -
?
(S)-mandelate + FMN
phenylglyoxylate + FMNH2
(S)-phenyllactate + 2,6-dichlorophenolindophenol
?
-
Substrates: -
Products: -
?
2-hydroxy-3-butynoate + acceptor
2-oxo-3-butynoate + reduced acceptor
2-hydroxybutyrate + acceptor
2-oxobutyrate + reduced acceptor
-
Substrates: -
Products: -
?
2-hydroxyhexanoate + acceptor
2-oxohexanoate + reduced acceptor
-
Substrates: -
Products: -
?
2-hydroxyisocaproate + acceptor
2-oxoisocaproate + reduced acceptor
-
Substrates: -
Products: -
?
2-hydroxyoctanoate + acceptor
2-oxooctanoate + reduced acceptor
-
Substrates: -
Products: -
?
2-hydroxyoctanoate + acceptor
? + reduced acceptor
Substrates: -
Products: -
?
2-hydroxyvalerate + acceptor
2-oxovalerate + reduced acceptor
-
Substrates: -
Products: -
?
3-hydroxy-DL-mandelate + ferricyanide
2-oxo-2-(3-hydroxyphenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
3-indolelactate + acceptor
3-(1H-indol-2-yl)-2-oxopropanoate + reduced acceptor
-
Substrates: -
Products: -
?
3-indolelactate + acceptor
? + reduced acceptor
Substrates: -
Products: -
?
3-methoxy-DL-mandelate + ferricyanide
2-oxo-2-(3-methoxyphenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
3-phenyllactate + acceptor
2-oxo-3-phenylpropanoate + reduced acceptor
-
Substrates: -
Products: -
?
4-bromo-DL-mandelate + ferricyanide
2-oxo-2-(4-bromophenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
4-chloro-DL-mandelate + ferricyanide
2-oxo-2-(4-chlorophenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
4-chloromandelate + acceptor
2-oxo-2-(4-chlorophenyl)acetate + reduced acceptor
-
Substrates: -
Products: -
?
4-fluoro-D,L-mandelate + ferricyanide
2-oxo-2-(4-fluorophenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
4-hydroxy-DL-mandelate + ferricyanide
2-oxo-2-(4-hydroxyphenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
4-methoxy-DL-mandelate + ferricyanide
2-oxo-2-(4-methoxyphenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
4-methyl-DL-mandelate + ferricyanide
2-oxo-2-(4-methylphenyl)acetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
DL-mandelate + ferricyanide
2-oxo-2-phenylacetate + ferrocyanide + H2O
-
Substrates: -
Products: -
?
ethyl-(S)-mandelate + acceptor
?
Substrates: -
Products: -
?
indoleglycolate + acceptor
indol-2-yl(oxo)acetate + reduced acceptor
-
Substrates: -
Products: -
?
L-mandelate + ferricyanide
2-oxo-2-phenylacetate + ferrocyanide
-
Substrates: -
Products: -
?
mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
methyl-(S)-mandelate + acceptor
?
Substrates: -
Products: -
?
additional information
?
-
(R,S)-2-hydroxy-3-butenoic acid + acceptor
2-oxo-3-butenoic acid + reduced acceptor
-
Substrates: -
Products: -
?
(R,S)-2-hydroxy-3-butenoic acid + acceptor
2-oxo-3-butenoic acid + reduced acceptor
Substrates: very low binding affinity for MDH
Products: -
?
(R,S)-2-hydroxyisovalerate + acceptor
2-oxo-isovalerate + reduced acceptor
-
Substrates: -
Products: -
?
(R,S)-2-hydroxyisovalerate + acceptor
2-oxo-isovalerate + reduced acceptor
Substrates: -
Products: -
?
(S)-mandelate + 2 ferricyanide
2-oxo-2-phenylacetate + 2 ferrocyanide + 2 H+
Substrates: -
Products: -
?
(S)-mandelate + 2 ferricyanide
2-oxo-2-phenylacetate + 2 ferrocyanide + 2 H+
-
Substrates: -
Products: -
?
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: reduction of 2,6-dichloroindophenol in presence of N-methylphenazonium methosulfate
Products: -
?
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: -
Products: -
?
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: -
Products: -
r
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: acceptor: 2,6-dichloroindophenol plus phenazine methosulfate. The MDH reaction has two rate-limiting step of similar activation energies: the formation and breakdown of a distinct intermediate, with the latter step being slightly more rate limiting. MDH is capable of catalyzing the reverse reaction, the reoxidation of reduced MDH by the product ketoacid, benzoylformate. The transient intermediate is observed during the reverse reaction as well
Products: -
r
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: phenazine methosulfate and 2,6-dichloroindophenol as acceptor. In absence of any other electron acceptor, oxygen is used by the wild-type enzyme for reoxidation of the reduced flavin, at a rather slow rate
Products: -
?
(S)-mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: reduction of 2,6-dichloroindophenol in presence of N-methylphenazonium methosulfate
Products: -
?
(S)-mandelate + FMN
phenylglyoxylate + FMNH2
-
Substrates: -
Products: -
?
(S)-mandelate + FMN
phenylglyoxylate + FMNH2
-
Substrates: -
Products: -
?
2-hydroxy-3-butynoate + acceptor
2-oxo-3-butynoate + reduced acceptor
-
Substrates: -
Products: -
?
2-hydroxy-3-butynoate + acceptor
2-oxo-3-butynoate + reduced acceptor
Substrates: -
Products: -
?
mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
-
Substrates: -
Products: -
?
mandelate + acceptor
2-oxo-2-phenylacetate + reduced acceptor
Substrates: -
Products: -
?
additional information
?
-
Substrates: (S)-mandelamide, (S)-1-phenyl-2-propen-1-ol, (S)-1-phenyl-1,2-ethanediol, (S)-1-phenyl-2-propyn-1-ol, (R,S)-pantoyllactone, and (S)-1-phenyl-2,2,2-trifluoroethanol are no substrates
Products: -
?
additional information
?
-
-
Substrates: (S)-mandelamide, (S)-1-phenyl-2-propen-1-ol, (S)-1-phenyl-1,2-ethanediol, (S)-1-phenyl-2-propyn-1-ol, (R,S)-pantoyllactone, and (S)-1-phenyl-2,2,2-trifluoroethanol are no substrates
Products: -
?
additional information
?
-
-
Substrates: enzyme-catalyzed reaction proceeds via the same transition state for each substrate and indicates that this transition state is relatively non-polar but has an electron-rich centre at the alpha-carbon position
Products: -
?
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22
(R,S)-2-hydroxy-3-butynoic acid
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
32
(R,S)-2-hydroxybutyrate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
4.9
(R,S)-2-hydroxyhexanoate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
4.3
(R,S)-2-hydroxyisocaproate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
9.5
(R,S)-2-hydroxyisovalerate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
0.75
(R,S)-2-hydroxyoctanoate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
15.3
(R,S)-2-hydroxyvalerate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
0.9
(R,S)-3-indolelactate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
0.4
(R,S)-indoleglycolate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
0.33
(R,S)-mandelate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
0.074 - 4.3
(S)-3-phenyllactate
0.78 - 2.6
(S)-phenyllactate
10.3
2-Hydroxy-3-butenoate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
4.3 - 22
2-Hydroxy-3-butynoate
4.4 - 32
2-Hydroxybutyrate
0.89 - 4.9
2-hydroxyhexanoate
0.49 - 4.3
2-hydroxyisocaproate
2.6
2-Hydroxyisovalerate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.14 - 0.8
2-Hydroxyoctanoate
3.2 - 15.3
2-hydroxyvalerate
0.08
3-hydroxy-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.13 - 0.9
3-indolelactate
0.12
3-methoxy-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.26
4-bromo-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.15 - 0.38
4-chloro-D,L-mandelate
0.27 - 0.43
4-chloromandelate
0.16
4-fluoro-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.12
4-methoxy-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.17
4-methyl-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.35
D,L-Mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
2
DL-3-phenyllactate
in 0.1 M potassium phosphate buffer, pH 7.5 at 20°C
0.47 - 0.78
DL-[2-1H]-mandelate
0.53 - 1.33
DL-[2-2H]-mandelate
2.7 - 3.7
ethyl-(S)-mandelate
3.87
ferricyanide
-
at pH 6.5 and 30°C
0.24 - 0.63
indoleglycolate
0.24
L-Mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
7.4 - 11.3
methyl-(S)-mandelate
0.074
(S)-3-phenyllactate
-
pH 7.5, 20°C, mutant enzyme R277G
4.3
(S)-3-phenyllactate
-
pH 7.5, 20°C, wild-type enzyme
0.04
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme, G81A/MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach and a G81A mutation in MDH
0.085
(S)-Mandelate
-
pH 7.5, 20°C, cosubstrate: 2,6-dichloroindophenol, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.09
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.11
(S)-Mandelate
-
pH 7.5, 4°C
0.12
(S)-Mandelate
-
pH 7.5, 20°C
0.12
(S)-Mandelate
-
pH 7.5, 20°C, wild-type enzyme
0.12
(S)-Mandelate
wild type enzyme, at 20°C, in 0.1 M potassium phosphate, pH 7.5
0.13
(S)-Mandelate
-
pH 7.5, 20°C, wild-type enzyme
0.15
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme G81A
0.158
(S)-Mandelate
-
pH 7.5, (S)-mandelate dehydrogenase with 17 residues deleted at the carboxy terminus
0.17
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme G81V
0.18
(S)-Mandelate
-
pH 7.5, 20°C, cosubstrate: 2,6-dichloroindophenol, wild-type enzyme
0.18
(S)-Mandelate
-
pH 7.5, 25°C, electron acceptor: 2,6-dichloroindophenol
0.206
(S)-Mandelate
-
pH 7.5, wild-type enzyme
0.225
(S)-Mandelate
-
pH 7.5, (S)-mandelate dehydrogenase with residues 2-4 deleted
0.229
(S)-Mandelate
-
pH 7.5, chimeric mutant of (S)-mandelate dehydrogenase with membrane anchoring loop replaced by a portion of glycolate oxidase from spinach
0.27
(S)-Mandelate
-
pH 7.5, 25°C, electron acceptor: ferricyanide
0.27
(S)-Mandelate
-
chitosan-immobilized enzyme, at pH 3.4 and 45°C
0.49
(S)-Mandelate
-
pH 7.5, 25°C, electron acceptor: cytochrome c
0.92
(S)-Mandelate
-
at pH 6.5 and 30°C
1.5
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R165K
2
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme G81D
2.3
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme G81S
4.4
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R165M
4.4
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R277K
5.6
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R277K
5.6
(S)-Mandelate
mutant enzyme R277K, at 20°C, in 0.1 M potassium phosphate, pH 7.5
5.8
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R165G
12
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R165E
13
(S)-Mandelate
-
mutant enzyme H274G, in presence of 20 mM imidazole
15.2
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R165K/R277K
17
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R277G
17
(S)-Mandelate
mutant enzyme R277G, at 20°C, in 0.1 M potassium phosphate, pH 7.5
19.2
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R277H
31.4
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R165G/R277K
47
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R277G
73
(S)-Mandelate
-
pH 7.5, 20°C, mutant enzyme R277L
0.78
(S)-phenyllactate
-
pH 7.5, chimeric mutant of (S)-mandelate dehydrogenase with membrane anchoring loop replaced by a portion of glycolate oxidase from spinach
2.6
(S)-phenyllactate
-
pH 7.5, wild-type enzyme
4.3
2-Hydroxy-3-butynoate
-
pH 7.5, 20°C, mutant enzyme G81A
17.2
2-Hydroxy-3-butynoate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
22
2-Hydroxy-3-butynoate
-
pH 7.5, 20°C, wild-type enzyme
4.4
2-Hydroxybutyrate
-
pH 7.5, 20°C, mutant enzyme G81A
13.2
2-Hydroxybutyrate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
32
2-Hydroxybutyrate
-
pH 7.5, 20°C, wild-type enzyme
0.89
2-hydroxyhexanoate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
1.4
2-hydroxyhexanoate
-
pH 7.5, 20°C, mutant enzyme G81A
4.9
2-hydroxyhexanoate
-
pH 7.5, 20°C, wild-type enzyme
0.49
2-hydroxyisocaproate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
1.6
2-hydroxyisocaproate
-
pH 7.5, 20°C, mutant enzyme G81A
4.3
2-hydroxyisocaproate
-
pH 7.5, 20°C, wild-type enzyme
0.14
2-Hydroxyoctanoate
-
pH 7.5, 20°C, mutant enzyme G81A
0.14
2-Hydroxyoctanoate
mutant G81A
0.29
2-Hydroxyoctanoate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.29
2-Hydroxyoctanoate
chimera MDH-GOX2
0.57
2-Hydroxyoctanoate
mutant G81A of chimera MDH-GOX2
0.8
2-Hydroxyoctanoate
wild-type enzyme
0.8
2-Hydroxyoctanoate
-
pH 7.5, 20°C, wild-type enzyme
3.2
2-hydroxyvalerate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
6.4
2-hydroxyvalerate
-
pH 7.5, 20°C, mutant enzyme G81A
15.3
2-hydroxyvalerate
-
pH 7.5, 20°C, wild-type enzyme
0.13
3-indolelactate
mutant G81A of chimera MDH-GOX2
0.17
3-indolelactate
-
pH 7.5, 20°C, mutant enzyme G81A
0.17
3-indolelactate
mutant G81A
0.64
3-indolelactate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.64
3-indolelactate
chimera MDH-GOX2
0.9
3-indolelactate
wild-type enzyme
0.9
3-indolelactate
-
pH 7.5, 20°C, wild-type enzyme
0.37
3-Phenyllactate
-
pH 7.5, 20°C, mutant enzyme G81A
1.3
3-Phenyllactate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
2
3-Phenyllactate
-
pH 7.5, 20°C, wild-type enzyme
0.15
4-chloro-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.38
4-chloro-D,L-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.27
4-chloromandelate
-
pH 7.5, 20°C, wild-type enzyme
0.43
4-chloromandelate
-
pH 7.5, 20°C, mutant enzyme G81A
0.47
DL-[2-1H]-mandelate
-
pH 7.5, 25°C, cosubstrate ferricyanide, LMDH holoenzyme
0.74
DL-[2-1H]-mandelate
-
pH 7.5, 25°C, cosubstrate ferricyanide, L-MDH flavin domain
0.78
DL-[2-1H]-mandelate
-
pH 7.5, 25°C, cosubstrate cytochrome c, LMDH holoenzyme
0.53
DL-[2-2H]-mandelate
-
pH 7.5, 25°C, cosubstrate ferricyanide, LMDH holoenzyme
0.74
DL-[2-2H]-mandelate
-
pH 7.5, 25°C, cosubstrate: ferricyanide
0.79
DL-[2-2H]-mandelate
-
pH 7.5, 25°C, cosubstrate ferricyanide, L-MDH flavin domain
1.33
DL-[2-2H]-mandelate
-
pH 7.5, 25°C, cosubstrate cytochrome, LMDH holoenzyme
2.7
ethyl-(S)-mandelate
mutant enzyme R277K, at 20°C, in 0.1 M potassium phosphate, pH 7.5
2.9
ethyl-(S)-mandelate
wild type enzyme, at 20°C, in 0.1 M potassium phosphate, pH 7.5
3.7
ethyl-(S)-mandelate
mutant enzyme R277G, at 20°C, in 0.1 M potassium phosphate, pH 7.5
0.24
indoleglycolate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.4
indoleglycolate
-
pH 7.5, 20°C, wild-type enzyme
0.63
indoleglycolate
-
pH 7.5, 20°C, mutant enzyme G81A
0.04
Mandelate
mutant G81A of chimera MDH-GOX2
0.09
Mandelate
chimera MDH-GOX2
0.14
Mandelate
-
pH 7.5, 20°C, MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
0.24
Mandelate
wild-type enzyme
0.24
Mandelate
-
pH 7.5, 20°C, mutant enzyme G81A
0.24
Mandelate
-
pH 7.5, 20°C, wild-type enzyme
0.24
Mandelate
mutant G81A
7.4
methyl-(S)-mandelate
mutant enzyme R277G, at 20°C, in 0.1 M potassium phosphate, pH 7.5
10.3
methyl-(S)-mandelate
mutant enzyme R277K, at 20°C, in 0.1 M potassium phosphate, pH 7.5
11.3
methyl-(S)-mandelate
wild type enzyme, at 20°C, in 0.1 M potassium phosphate, pH 7.5
0.04
O2
-
pH 7.5, 20°C, mutant enzyme G81V
0.22
O2
-
pH 7.5, 20°C, mutant enzyme G81D
0.49
O2
-
pH 7.5, 20°C, mutant enzyme, G81A/MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach and a G81A mutation in MDH
0.68
O2
-
pH 7.5, 20°C, mutant enzyme MDH-GOX2, a chimeric mutant of (S)-mandelate dehydrogenase with 205 residues 177-215 replaced by residues 176-195 of glycolate oxidase from spinach
1.1
O2
-
pH 7.5, 20°C, mutant enzyme G81A
1.4
O2
-
pH 7.5, 20°C, mutant enzyme G81S
3.2
O2
-
pH 7.5, 20°C, wild-type enzyme
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