17215925
ChemSpider
1.0
C3H6O2
(S)-lactaldehyde
74.03678
Lactaldehyde dehydrogenase
937
ChemSpider
L-lactate dehydrogenase [cytochrome]
SMILES
NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O
96860
ChemSpider
SMP0000807
SMPDB
2,5-diketo-D-gluconic acid reductase A
880
PubChem-compound
5682
ChemSpider
2,5-diketo-D-gluconic acid reductase B
SMILES
NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
NADH
Water
439153
PubChem-compound
METHYL-GLYOXAL
BioCyc
SMILES
O
1.0
1.0
1.0
Reduced acceptor
PW002078
PathWhiz
NAD
CHEBI:18041
ChEBI
5675
ChemSpider
ReactionCatalysis2942
ACTIVATION
ReactionCatalysis2944
ACTIVATION
Pyruvic acid
SubPathwayInput
CHEBI:15846
ChEBI
1.1.-.-
false
1.1.-.-
L-Lactic acid + oxidized electron acceptor → Pyruvic acid + Reduced acceptor
LEFT_TO_RIGHT
1.2.1.22
false
1.2.1.22
(S)-lactaldehyde + NAD + Water → 2 Hydrogen Ion + L-Lactic acid + NADH
LEFT_TO_RIGHT
C3H4O3
Pyruvic acid
88.016045
methylglyoxal reductase
53-59-8
CAS
P30863
UniProt
78-98-8
CAS
P25553
UniProt
Escherichia coli
1038
PubChem-compound
7732-18-5
CAS
388299
ChemSpider
1.0
Q46857
UniProt
Reduced acceptor
CHEBI:16474
ChEBI
CHEBI:15022
ChEBI
HMDB0001487
HMDB
79-33-4
CAS
127-17-3
CAS
1.0
1.0
CHEBI:16908
ChEBI
Lactaldehyde dehydrogenase
C00186
KEGG Compound
NADPH
1.0
1010
ChemSpider
SMILES
CC(=O)C(O)=O
NADP
C21H30N7O17P3
NADPH
745.0911
L-LACTATE
BioCyc
C21H29N7O17P3
NADP
744.08325
4.0
962
PubChem-compound
1.0
1.0
NADPH
BioCyc
Methylglyoxal Degradation IV
Reaction6073
false
Hydrogen Ion + NADPH + Pyruvaldehyde → (S)-lactaldehyde + NADP
LEFT_TO_RIGHT
Hydrogen Ion
PW000785
PathWhiz
857
ChemSpider
C3H4O2
Pyruvaldehyde
72.021126
5893
PubChem-compound
58-68-4
CAS
C00080
KEGG Compound
HMDB0000217
HMDB
P33232
UniProt
HMDB0002111
HMDB
CHEBI:32816
ChEBI
CHEBI:15377
ChEBI
CHEBI:17158
ChEBI
2,5-diketo-D-gluconic acid reductase A
CHEBI:15378
ChEBI
SMILES
[H+]
C00006
KEGG Compound
L-lactate dehydrogenase [cytochrome]
PYRUVATE
BioCyc
CHEBI:18009
ChEBI
oxidized electron acceptor
C00001
KEGG Compound
5886
PubChem-compound
C00005
KEGG Compound
C00004
KEGG Compound
2,5-diketo-D-gluconic acid reductase B
C00003
KEGG Compound
1031
ChemSpider
SMILES
NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
HMDB0000221
HMDB
1.0
CHEBI:422
ChEBI
SMILES
NC(=O)C1=CN(C=CC1)[C@H]1O[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2O[C@@H]([C@@H](OP(O)(O)=O)[C@H]2O)N2C=NC3=C(N)N=CN=C23)[C@H](O)[C@@H]1O
L-Lactic acid
C3H6O3
L-Lactic acid
90.03169
53-57-6
CAS
SMILES
CC(=O)C=O
Glycolysis and Pyruvate Dehydrogenase
SubPathway
C21H28N7O14P2
NAD
664.11694
HMDB0000190
HMDB
107689
PubChem-compound
SMILES
CC(O)C=O
HMDB0000902
HMDB
aldehyde dehydrogenase A, NAD-linked
HMDB0001167
HMDB
22833512
PubChem-compound
NAD(P)
BioCyc
C21H29N7O14P2
NADH
665.12476
H2O
Water
18.010565
ReactionCatalysis6035
ACTIVATION
NADH
BioCyc
562
TAXONOMY
NAD
BioCyc
2.0
Pyruvaldehyde
1060
PubChem-compound
H
Hydrogen Ion
1.007825
C00546
KEGG Compound
(S)-lactaldehyde
HMDB0059597
HMDB
oxidized electron acceptor
C00022
KEGG Compound
53-84-9
CAS
HMDB0000243
HMDB
SMP0002090
SMPDB
SMILES
C[C@@H](O)C(O)=O
1.0
SubPathwayInteraction109941
SubPathway109941Reaction
SubPathwayReaction