1.2.1.19: aminobutyraldehyde dehydrogenase
This is an abbreviated version!
For detailed information about aminobutyraldehyde dehydrogenase, go to the full flat file.
Word Map on EC 1.2.1.19
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1.2.1.19
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badhs
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choline
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osmoprotectant
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1.2.1.8
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spinacia
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2-acetyl-1-pyrroline
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glycinebetaine
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3-aminopropionaldehyde
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suaeda
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halophyte
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fragrant
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hypochondriacus
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aldh10s
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amaranthus
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liaotungensis
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jasmine
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basmati
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4-aminobutyrate
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synthesis
- 1.2.1.19
-
badhs
- choline
-
osmoprotectant
-
1.2.1.8
-
spinacia
-
2-acetyl-1-pyrroline
- glycinebetaine
- 3-aminopropionaldehyde
-
suaeda
-
halophyte
-
fragrant
-
hypochondriacus
- aldh10s
-
amaranthus
-
liaotungensis
-
jasmine
-
basmati
- 4-aminobutyrate
- synthesis
Reaction
Synonyms
4-aminobutanal dehydrogenase, 4-aminobutyraldehyde dehydrogenase, ABAL dehydrogenase, ABALDH, ALDH10A8, ALDH10A9, AMADH, AMADH1, AMADH2, aminoaldehyde dehydrogenase, BADH, betaine aldehyde dehydrogenase, dehydrogenase, aminobutyraldehyde, EC 1.5.1.35, gadbh, gamma-aminobutanal dehydrogenase, gamma-aminobutyraldehyde dehydroganase, gamma-aminobutyraldehyde dehydrogenase, gamma-guanidinobutyraldehyde dehydrogenase, MdAMADH1, MdAMADH2, More, NAD+-aminoaldehyde dehydrogenase, NAD+-dependent aminoaldehyde dehydrogenase, PatD, PsAMADH 1, PsAMADH 2, SlAMADH1, SlAMADH2, YdcW, ZmAMADH1a, ZmAMADH1b, ZmAMADH2
ECTree
1.2.1.19 aminobutyraldehyde dehydrogenaseAdvanced search results
results (
results (KM Value
KM Value on EC 1.2.1.19 - aminobutyraldehyde dehydrogenase
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KM VALUE [mM] 
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
IMAGE
0.506
2,2-dimethyl-4-propionylaminobutanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.003
capronaldehyde
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same value with benzaldehyde, constant substrate 1 mM NAD+
0.266
2,2-dimethyl-3-propionylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.477
2,2-dimethyl-3-propionylaminopropanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.366
2-methyl-3-butyrylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.397
2-methyl-3-butyrylaminopropanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.469
2-methyl-3-butyrylaminopropanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.638
2-methyl-3-butyrylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.0935
2-methyl-3-propionylaminopropanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.183
2-methyl-3-propionylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.189
2-methyl-4-propionylaminobutanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.525
2-methyl-4-propionylaminobutanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.0086
3-aminopropanal
pH 9.8, temperature not specified in the publication, isozyme MdAMADH2
0.016
3-aminopropanal
pH 9.8, temperature not specified in the publication, isozyme MdAMADH1
0.01
3-aminopropionaldehyde
isozyme AMADH2, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.0148
3-aminopropionaldehyde
pH 8.0, 30°C, recombinant isozyme LrAMADH1
0.0259
3-aminopropionaldehyde
pH 8.0, 30°C, recombinant isozyme LrAMADH1
0.075
3-aminopropionaldehyde
isozyme AMADH1, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.13
3-methyl-3-butyrylaminopropanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.137
3-methyl-3-butyrylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.361
3-methyl-3-butyrylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.531
3-methyl-3-butyrylaminopropanal
isozyme PsAMADH 2, pH 9.0, 30°C
0.49 - 2
3-propionylaminopropanal
isozyme PsAMADH 1, pH 9.0, 30°C
0.0848
4-aminobutanal
pH 9.8, temperature not specified in the publication, isozyme MdAMADH1
0.16
4-aminobutanal
pH 9.8, temperature not specified in the publication, isozyme MdAMADH2
0.00394
4-Aminobutyraldehyde
pH 8.0, 30°C, recombinant isozyme LrAMADH1
0.018
4-Aminobutyraldehyde
-
250 mM phosphate preparation, constant substrate 1 mM NAD+
0.029
4-Aminobutyraldehyde
isozyme AMADH2, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.0312
4-Aminobutyraldehyde
pH 8.0, 30°C, recombinant isozyme LrAMADH1
0.081
4-Aminobutyraldehyde
-
400 mM phosphate preparation, constant substrate 1 mM NAD+
0.17
4-Aminobutyraldehyde
isozyme AMADH1, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.007
4-guanidinobutyraldehyde
isozyme AMADH2, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.011
4-guanidinobutyraldehyde
isozyme AMADH1, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.054
acetaldehyde
-
250 mM phosphate preparation, constant substrate 1 mM NAD+
6.9
acetaldehyde
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400 mM phosphate preparation, constant substrate 1 mM NAD+
0.285
Betaine aldehyde
-
250 mM phosphate preparation, constant substrate 1 mM NAD+
0.01
N,N,N-trimethyl-4-aminobutyraldehyde
isozyme AMADH1, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.021
N,N,N-trimethyl-4-aminobutyraldehyde
isozyme AMADH2, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.0132
NAD+
with 4-aminobutanal, pH 8.5, 22°C, recombinant enzyme
0.0208
NAD+
with 3-aminopropanal, pH 8.5, 22°C, recombinant enzyme
0.0338
NAD+
pH 9.8, temperature not specified in the publication, isozyme MdAMADH1
0.04
NAD+
isozyme AMADH1, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.055
NAD+
isozyme AMADH2, in 0.15 M Tris-HCl buffer (pH 9.0), at 20°C
0.0736
NAD+
with 3-aminopropanal, pH 9.5, 22°C, recombinant enzyme
0.0828
NAD+
pH 9.8, temperature not specified in the publication, isozyme MdAMADH2
0.086
NAD+
with 4-aminobutanal, pH 9.5, 22°C, recombinant enzyme
0.252
Succinic semialdehyde
-
400 mM phosphate preparation, constant substrate 1 mM NAD+
5.428
Succinic semialdehyde
-
250 mM phosphate preparation, constant substrate 1 mM NAD+
additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
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Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
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Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics, except for LrAMADH1 on 4-aminobutyraldehyde
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additional information
additional information
Michaelis-Menten kinetics, except for LrAMADH1 on 4-aminobutyraldehyde
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additional information
additional information
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Michaelis-Menten kinetics, except for LrAMADH1 on 4-aminobutyraldehyde
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