CHEBI:16015
ChEBI
30572
ChemSpider
C5H11O7P
1-Deoxy-D-xylulose 5-phosphate
214.02425
C00314
KEGG Compound
6022
PubChem-compound
7722-84-1
CAS
PW002488
PathWhiz
937
ChemSpider
CHEBI:16493
ChEBI
Pyridoxal 5'-phosphate
C3H8NO5P
2-Amino-3-phosphonopropionic acid
169.014
NADH
CHEBI:27951
ChEBI
4.0
HMDB0003125
HMDB
1.0
erythrose 4-phosphate dehydrogenase
439153
PubChem-compound
SMILES
O
CHEBI:28803
ChEBI
SMILES
OO
1.0
2-Amino-3-oxo-4-phosphonooxybutyrate
SMP0002387
SMPDB
50
ChemSpider
1.0
P00360
UniProt
NAD
HMDB0000538
HMDB
ATP
BioCyc
Pyridoxine 5'-phosphate
H4N
Ammonium
18.034374
1.0
Pyridoxine
1.0
66-72-8
CAS
51
PubChem-compound
Pyruvic acid
Unknown
CHEBI:15846
ChEBI
ADP
BioCyc
C3H4O3
Pyruvic acid
88.016045
1.0
C8H11NO3
Pyridoxine
169.0739
1026
ChemSpider
1025
ChemSpider
1024
ChemSpider
1.0
NADH
5742
ChemSpider
1038
PubChem-compound
1023
ChemSpider
1022
ChemSpider
1021
ChemSpider
1.4.3.5
false
1.4.3.5
Oxygen + Pyridoxine 5'-phosphate → Hydrogen peroxide + Pyridoxal 5'-phosphate
LEFT_TO_RIGHT
952
ChemSpider
GO:0005829
GENE ONTOLOGY
Reaction6965
false
Adenosine triphosphate + Pyridoxal → Adenosine diphosphate + Pyridoxal 5'-phosphate
LEFT_TO_RIGHT
Reaction6966
false
Oxygen + Pyridoxamine 5'-phosphate + Water → Ammonium + Hydrogen peroxide + Pyridoxal 5'-phosphate
LEFT_TO_RIGHT
2-Amino-3-phosphonopropionic acid
PYRIDOXAL_PHOSPHATE
BioCyc
Reaction6967
false
Adenosine triphosphate + Pyridoxamine → Adenosine diphosphate + Pyridoxamine 5'-phosphate
LEFT_TO_RIGHT
2.2.1.7
false
2.2.1.7
D-Glyceraldehyde 3-phosphate + Hydrogen Ion + Pyruvic acid → 1-Deoxy-D-xylulose 5-phosphate + Carbon dioxide
LEFT_TO_RIGHT
274
ChemSpider
C5H6O5
Oxoglutaric acid
146.02153
4-Phospho-D-erythronate
Reaction6960
false
2-Oxo-3-hydroxy-4-phosphobutanoic acid + L-Glutamic acid ↔ O-Phospho-4-hydroxy-L-threonine + Oxoglutaric acid
REVERSIBLE
1.0
1.1.1.262
false
1.1.1.262
NAD + O-Phospho-4-hydroxy-L-threonine → 2-Amino-3-oxo-4-phosphonooxybutyrate + Hydrogen Ion + NADH
LEFT_TO_RIGHT
C4H8NO7P
2-Amino-3-oxo-4-phosphonooxybutyrate
213.00385
2.6.99.2
false
2.6.99.2
1-Deoxy-D-xylulose 5-phosphate + 2-Amino-3-phosphonopropionic acid → Hydrogen Ion + Phosphate + Pyridoxine 5'-phosphate + 2 Water
LEFT_TO_RIGHT
CHEBI:16908
ChEBI
2.7.1.35
false
2.7.1.35
Adenosine triphosphate + Pyridoxine → Adenosine diphosphate + Hydrogen Ion + Pyridoxine 5'-phosphate
LEFT_TO_RIGHT
709
ChemSpider
O4P
Phosphate
94.95342
CHEBI:244030
ChEBI
CHEBI:16240
ChEBI
C8H12N2O2
Pyridoxamine
168.08987
1-Deoxy-D-xylulose 5-phosphate
1010
ChemSpider
Saccharomyces cerevisiae
1.2.1.72
false
1.2.1.72
D-Erythrose 4-phosphate + NAD + Water → 4-Phospho-D-erythronate + Hydrogen Ion + NADH
LEFT_TO_RIGHT
1.1.1.290
false
1.1.1.290
4-Phospho-D-erythronate + NAD → 2-Oxo-3-hydroxy-4-phosphobutanoic acid + Hydrogen Ion + NADH
LEFT_TO_RIGHT
529-96-4
CAS
Reaction3327
true
2-Amino-3-oxo-4-phosphonooxybutyrate + Hydrogen Ion → 2-Amino-3-phosphonopropionic acid + Carbon dioxide
LEFT_TO_RIGHT
C3H7O6P
D-Glyceraldehyde 3-phosphate
169.99803
Ammonium
CPD-455
BioCyc
Hydrogen Ion
21145142
PubChem-compound
HMDB0000208
HMDB
Cytosol
CPD-6641
BioCyc
1.0
218
ChemSpider
Adenosine triphosphate
58-68-4
CAS
PYRIDOXAMINE-5P
BioCyc
Pyridoxal
L-Glutamic acid
SMILES
[O-]P([O-])([O-])=O
HMDB0001545
HMDB
SMILES
OC(=O)CCC(=O)C(O)=O
Oxygen
CHEBI:30915
ChEBI
124-38-9
CAS
Pyridoxal kinase
4-hydroxy-L-threonine phosphate dehydrogenase, NAD-dependent
Pyridoxine 5'-phosphate synthase
3-phosphoserine aminotransferase / phosphohydroxythreonine aminotransferase
C00009
KEGG Compound
C00008
KEGG Compound
C00007
KEGG Compound
Hydrogen Ion
C00001
KEGG Compound
HMDB0001429
HMDB
122357
PubChem-compound
1.0
SMILES
CC1=C(O)C(CN)=C(CO)C=N1
C00004
KEGG Compound
CHEBI:18367
ChEBI
C00003
KEGG Compound
C4H7O8P
2-Oxo-3-hydroxy-4-phosphobutanoic acid
213.98785
1032
ChemSpider
C4H10NO7P
O-Phospho-4-hydroxy-L-threonine
215.01949
C00002
KEGG Compound
1031
ChemSpider
HMDB0001431
HMDB
HMDB0001555
HMDB
Pyridoxine 5'-phosphate oxidase
C00250
KEGG Compound
1-deoxyxylulose-5-phosphate synthase
GLT
BioCyc
1.0
1.0
C00018
KEGG Compound
CHEBI:18335
ChEBI
1.0
CHEBI:18336
ChEBI
O-Phospho-4-hydroxy-L-threonine
C21H28N7O14P2
NAD
664.11694
441260
PubChem-compound
1.0
HMDB0001319
HMDB
C00011
KEGG Compound
SMILES
O=C=O
C8H12NO6P
Pyridoxine 5'-phosphate
249.04022
C01342
KEGG Compound
CHEBI:16273
ChEBI
443201
PubChem-compound
CHEBI:28938
ChEBI
C4H9O7P
D-Erythrose 4-phosphate
200.00859
HMDB0000902
HMDB
2-Oxo-3-hydroxy-4-phosphobutanoic acid
HMDB0001321
HMDB
C21H29N7O14P2
NADH
665.12476
HMDB0000239
HMDB
5957
PubChem-compound
CHEBI:16709
ChEBI
CHEBI:17138
ChEBI
H
Hydrogen Ion
1.007825
696
PubChem-compound
D-Glyceraldehyde 3-phosphate
ERYTHROSE-4P
BioCyc
C8H10NO6P
Pyridoxal 5'-phosphate
247.02457
C00022
KEGG Compound
56-65-5
CAS
53-84-9
CAS
C00027
KEGG Compound
C00026
KEGG Compound
C00025
KEGG Compound
PYRIDOXAL
BioCyc
DEOXYXYLULOSE-5P
BioCyc
Adenosine diphosphate
HMDB0000243
HMDB
HMDB0001213
HMDB
5652-28-8
CAS
C10H15N5O10P2
Adenosine diphosphate
427.02942
54-47-7
CAS
PYRIDOXAMINE
BioCyc
CHEBI:16410
ChEBI
Formate dehydrogenase 2
1.0
SMILES
O[C@H](COP(O)(O)=O)[C@@H](O)C=O
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
CPD-8587
BioCyc
SMILES
CC1=NC=C(COP(O)(O)=O)C(CO)=C1O
C00279
KEGG Compound
5682
ChemSpider
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
328-50-7
CAS
Water
Hydrogen peroxide
SMILES
CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O
HYDROGEN-PEROXIDE
BioCyc
HMDB0000370
HMDB
SMILES
[H][C@@](N)(C(O)=O)C(=O)COP(O)(O)=O
8.0
HMDB0001341
HMDB
1.0
389731
ChemSpider
D-Erythrose 4-phosphate
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
65-23-6
CAS
HMDB0001112
HMDB
763
ChemSpider
HMDB0000148
HMDB
14798-03-9
CAS
1.0
HMDB0006801
HMDB
Glyceraldehyde-3-phosphate dehydrogenase 1
HMDB0006802
HMDB
1.0
3723
ChemSpider
784
PubChem-compound
CHEBI:15422
ChEBI
85-87-0
CAS
7732-18-5
CAS
388299
ChemSpider
1.0
SMILES
CC(=O)[C@@H](O)[C@H](O)COP(O)(O)=O
591-59-3
CAS
CHEBI:48153
ChEBI
HMDB0001487
HMDB
O2
Oxygen
31.98983
1.0
127-17-3
CAS
C8H9NO3
Pyridoxal
167.05824
585-18-2
CAS
56-86-0
CAS
3857
PubChem-compound
CHEBI:49003
ChEBI
SMILES
NC(CP(O)(O)=O)C(O)=O
SMILES
[H][C@@](O)(COP(O)(O)=O)[C@@]([H])(O)C(O)=O
Water
C5H9NO4
L-Glutamic acid
147.05316
1.0
33032
PubChem-compound
NAD
SMILES
[NH4+]
C10H16N5O13P3
Adenosine triphosphate
506.99576
1.0
C00627
KEGG Compound
CHEBI:16526
ChEBI
1.0
1.0
CHEBI:16761
ChEBI
7782-44-7
CAS
HMDB0001377
HMDB
SMILES
CC(=O)C(O)=O
C06055
KEGG Compound
C8H13N2O5P
Pyridoxamine 5'-phosphate
248.05621
C06054
KEGG Compound
Pyridoxamine 5'-phosphate
391473
ChemSpider
1.0
HMDB0001491
HMDB
SMILES
CC1=C(O)C(CO)=C(CO)C=N1
962
PubChem-compound
1050
PubChem-compound
1051
PubChem-compound
1052
PubChem-compound
2-KETOGLUTARATE
BioCyc
5800
ChemSpider
1.0
Unknown
440901
PubChem-compound
CO2
Carbon dioxide
43.98983
1053
PubChem-compound
4-Phospho-D-erythronate
P0CT22
UniProt
Phosphate
1054
PubChem-compound
5893
PubChem-compound
1055
PubChem-compound
1.0
Pyridoxamine
ReactionCatalysis6936
ACTIVATION
2.0
SMILES
CC1=NC=C(CO)C(C=O)=C1O
ReactionCatalysis6935
ACTIVATION
C00080
KEGG Compound
SMILES
O=O
Oxoglutaric acid
ReactionCatalysis6939
ACTIVATION
ReactionCatalysis6938
ACTIVATION
ReactionCatalysis6937
ACTIVATION
729
PubChem-compound
HMDB0002111
HMDB
SMILES
N[C@@H](CCC(O)=O)C(O)=O
CHEBI:32816
ChEBI
C4H9O8P
4-Phospho-D-erythronate
216.00351
CHEBI:15377
ChEBI
C00647
KEGG Compound
1.0
CHEBI:15379
ChEBI
CHEBI:15378
ChEBI
SMILES
[H+]
14265-44-2
CAS
PYRUVATE
BioCyc
CHEBI:18405
ChEBI
58-64-0
CAS
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
CHEBI:17310
ChEBI
1.0
1.0
SMILES
CC1=NC=C(COP(O)(O)=O)C(CN)=C1O
1.0
ReactionCatalysis6945
ACTIVATION
190079-18-6
CAS
ReactionCatalysis6944
ACTIVATION
1.0
280
PubChem-compound
Formate dehydrogenase 2
Glyceraldehyde-3-phosphate dehydrogenase 1
ReactionCatalysis6943
ACTIVATION
ReactionCatalysis6942
ACTIVATION
Vitamin B6
ReactionCatalysis6941
ACTIVATION
447-05-2
CAS
ReactionCatalysis6940
ACTIVATION
1.0
C00534
KEGG Compound
4932
TAXONOMY
4.0
16741146
PubChem-compound
SMILES
OC(COP(O)(O)=O)C=O
PYRIDOXINE-5P
BioCyc
C05672
KEGG Compound
H2O
Water
18.010565
H2O2
Hydrogen peroxide
34.005478
NADH
BioCyc
NAD
BioCyc
GAP
BioCyc
1060
PubChem-compound
1061
PubChem-compound
977
PubChem-compound
HMDB0059597
HMDB
HMDB0041827
HMDB
Carbon dioxide
C00661
KEGG Compound
SMILES
O[C@H](COP(O)(O)=O)C(=O)C(O)=O
HMDB0001967
HMDB
109096
ChemSpider
SMILES
N[C@@H]([C@H](O)COP(O)(O)=O)C(O)=O
C11437
KEGG Compound
2.0