CHEBI:16015
ChEBI
30572
ChemSpider
1.0
7722-84-1
CAS
6022
PubChem-compound
C00314
KEGG Compound
3702
TAXONOMY
937
ChemSpider
1.0
Pyridoxal 5'-phosphate
CHEBI:16134
ChEBI
HMDB0003125
HMDB
Pyridoxal
CHEBI:27951
ChEBI
SMILES
O
SMILES
OO
CHEBI:28803
ChEBI
H3N
Ammonia
17.026548
1.0
50
ChemSpider
1.0
58838673
PubChem-compound
HMDB0000538
HMDB
ATP
BioCyc
5961
PubChem-compound
1.0
Pyridoxine 5'-phosphate
Phosphate
Pyridoxine
SubPathwayOutput
66-72-8
CAS
Water
51
PubChem-compound
Phosphoserine aminotransferase 1, chloroplastic
ADP
BioCyc
Pyridoxamine
1.0
C8H11NO3
Pyridoxine
169.0739
1026
ChemSpider
1025
ChemSpider
1024
ChemSpider
5746
ChemSpider
1.0
3.0
Inorganic pyrophosphatase 2
5742
ChemSpider
439184
PubChem-compound
1.0
1023
ChemSpider
1022
ChemSpider
1021
ChemSpider
952
ChemSpider
PYRIDOXAL_PHOSPHATE
BioCyc
ALPHA-GLUCOSE-16-BISPHOSPHATE
BioCyc
GO:0009507
GENE ONTOLOGY
1.0
C5H6O5
Oxoglutaric acid
146.02153
D-Glyceraldehyde 3-phosphate
SubPathwayOutput
1.0
709
ChemSpider
O4P
Phosphate
94.95342
CHEBI:16240
ChEBI
C8H12N2O2
Pyridoxamine
168.08987
1.0
D-Ribulose 5-phosphate
SubPathwayOutput
Oxygen
529-96-4
CAS
Pyridoxamine
CHEBI:28330
ChEBI
C3H7O6P
D-Glyceraldehyde 3-phosphate
169.99803
CPD-455
BioCyc
C5H10N2O3
L-Glutamine
146.06914
Pyridoxal 5'-phosphate
HMDB0000208
HMDB
21145142
PubChem-compound
L-Glutamic acid
CPD-6641
BioCyc
217
ChemSpider
PYRIDOXAMINE-5P
BioCyc
Pyridoxal
1.0
SMILES
[O-]P([O-])([O-])=O
HMDB0001545
HMDB
SMILES
OC(=O)CCC(=O)C(O)=O
CHEBI:30915
ChEBI
C00009
KEGG Compound
C00008
KEGG Compound
C00007
KEGG Compound
Hydrogen peroxide
ReactionCatalysis98529
ACTIVATION
1.0
HMDB0001429
HMDB
C00001
KEGG Compound
Q8W1X2
UniProt
SMILES
CC1=C(O)C(CN)=C(CO)C=N1
Pyridoxine 5'-phosphate
CHEBI:18367
ChEBI
1032
ChemSpider
C4H7O8P
2-Oxo-3-hydroxy-4-phosphobutanoic acid
213.98785
C00002
KEGG Compound
C4H10NO7P
O-Phospho-4-hydroxy-L-threonine
215.01949
ReactionCatalysis98530
ACTIVATION
HMDB0001431
HMDB
ReactionCatalysis98531
ACTIVATION
HMDB0001555
HMDB
C00250
KEGG Compound
GLN
BioCyc
GLT
BioCyc
7664-41-7
CAS
1.0
H2
Hydrogen
2.01565
C00018
KEGG Compound
CHEBI:18335
ChEBI
CHEBI:18336
ChEBI
Adenosine triphosphate
ReactionCatalysis98538
ACTIVATION
HMDB0001319
HMDB
C8H12NO6P
Pyridoxine 5'-phosphate
249.04022
ReactionCatalysis98539
ACTIVATION
ReactionCatalysis98536
ACTIVATION
ReactionCatalysis98537
ACTIVATION
ReactionCatalysis98534
ACTIVATION
222
PubChem-compound
ReactionCatalysis98535
ACTIVATION
CHEBI:17363
ChEBI
C00014
KEGG Compound
ReactionCatalysis98532
ACTIVATION
ReactionCatalysis98533
ACTIVATION
1.0
ReactionCatalysis98541
ACTIVATION
ReactionCatalysis98540
ACTIVATION
1.0
1.0
HMDB0000239
HMDB
5957
PubChem-compound
O80448
UniProt
CHEBI:16709
ChEBI
1.0
CHEBI:17138
ChEBI
Vitamin B6 Metabolism
C8H10NO6P
Pyridoxal 5'-phosphate
247.02457
SMILES
OCC(=O)[C@H](O)[C@H](O)COP(O)(O)=O
56-65-5
CAS
C00027
KEGG Compound
C00026
KEGG Compound
C00025
KEGG Compound
PYRIDOXAL
BioCyc
Pyridoxine/pyridoxamine 5'-phosphate oxidase 1, chloroplastic
1.0
54-47-7
CAS
Water
C10H15N5O10P2
Adenosine diphosphate
427.02942
GO:0005737
GENE ONTOLOGY
4151-19-3
CAS
Pyridoxal kinase
Threonine synthase 2
PYRIDOXAMINE
BioCyc
Reaction108428
false
Phosphate + Pyridoxine → Pyridoxine 5'-phosphate + Water
LEFT_TO_RIGHT
CHEBI:16410
ChEBI
Pyridoxamine 5'-phosphate
4.2.3.1
false
4.2.3.1
O-Phospho-4-hydroxy-L-threonine + Water → 4-Hydroxy-L-threonine + Phosphate
LEFT_TO_RIGHT
SubPathwayInteraction57043
SubPathway57043Reaction
SubPathwayReaction
SubPathwayInteraction57046
SubPathwayReaction
SubPathway57046Reaction
SubPathwayInteraction57044
SubPathway57044Reaction
SubPathwayReaction
SubPathwayInteraction57045
SubPathway57045Reaction
SubPathwayReaction
Reaction108420
false
Oxygen + Pyridoxine 5'-phosphate → Hydrogen peroxide + Pyridoxal 5'-phosphate
LEFT_TO_RIGHT
Reaction108421
false
Oxygen + Pyridoxamine + Water → Ammonia + Hydrogen + Pyridoxal
LEFT_TO_RIGHT
CPD-8587
BioCyc
1.4.3.5
false
1.4.3.5
Oxygen + Pyridoxine ↔ Hydrogen peroxide + Pyridoxal
REVERSIBLE
3.1.3.74
false
3.1.3.74
Phosphate + Pyridoxamine → Pyridoxamine 5'-phosphate + Water
LEFT_TO_RIGHT
SMILES
CC1=NC=C(COP(O)(O)=O)C(CO)=C1O
2.7.1.35
false
2.7.1.35
Adenosine triphosphate + Pyridoxamine → Adenosine diphosphate + Pyridoxamine 5'-phosphate
LEFT_TO_RIGHT
Reaction108425
false
Adenosine triphosphate + Pyridoxine → Adenosine diphosphate + Pyridoxine 5'-phosphate
LEFT_TO_RIGHT
CHEBI:18276
ChEBI
Reaction108426
false
Adenosine triphosphate + Pyridoxal → Adenosine diphosphate + Pyridoxal 5'-phosphate
LEFT_TO_RIGHT
L-Glutamic acid
Reaction108427
false
Pyridoxal 5'-phosphate + Water → Phosphate + Pyridoxal
LEFT_TO_RIGHT
328-50-7
CAS
Water
SMILES
CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O
Pyridoxine
C00282
KEGG Compound
HYDROGEN-PEROXIDE
BioCyc
1.0
2.6.1.52
false
2.6.1.52
O-Phospho-4-hydroxy-L-threonine + Oxoglutaric acid → 2-Oxo-3-hydroxy-4-phosphobutanoic acid + L-Glutamic acid
LEFT_TO_RIGHT
Phosphoserine aminotransferase 1, chloroplastic
HMDB0001341
HMDB
Glyoxylate and dicarboxylate metabolism
SubPathway
389731
ChemSpider
1.0
L-Glutamine
Glycolysis
SubPathway
Pentose phosphate pathway
SubPathway
56-85-9
CAS
Pentose phosphate pathway
SubPathway
1.0
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
HMDB0001112
HMDB
65-23-6
CAS
763
ChemSpider
Pyridoxal
762
ChemSpider
HMDB0000148
HMDB
Pyridoxal 5'-phosphate
HMDB0006801
HMDB
HMDB0006802
HMDB
Cytoplasm
Oxoglutaric acid
193577
PubChem-compound
784
PubChem-compound
CHEBI:15422
ChEBI
85-87-0
CAS
Arabidopsis thaliana
7732-18-5
CAS
591-59-3
CAS
O2
Oxygen
31.98983
C8H9NO3
Pyridoxal
167.05824
AMMONIA
BioCyc
SMILES
N
56-86-0
CAS
SMILES
N[C@@H]([C@H](O)CO)C(O)=O
Adenosine diphosphate
HMDB0001362
HMDB
C5H9NO4
L-Glutamic acid
147.05316
33032
PubChem-compound
Inorganic pyrophosphatase 2
SMP0063472
SMPDB
4.3.3.6
false
4.3.3.6
D-Glyceraldehyde 3-phosphate + D-Ribulose 5-phosphate + L-Glutamine → L-Glutamic acid + Phosphate + Pyridoxal 5'-phosphate + 3 Water
LEFT_TO_RIGHT
1.4.3.5
false
1.4.3.5
Oxygen + Pyridoxamine 5'-phosphate + Water → Ammonia + Hydrogen peroxide + Pyridoxal 5'-phosphate
LEFT_TO_RIGHT
1.0
Pyridoxal kinase
C10H16N5O13P3
Adenosine triphosphate
506.99576
Threonine synthase 2
C00627
KEGG Compound
Pyridoxal 5'-phosphate synthase subunit PDX1.1
O-Phospho-4-hydroxy-L-threonine
Pyridoxine/pyridoxamine 5'-phosphate oxidase 1, chloroplastic
C00064
KEGG Compound
CHEBI:16761
ChEBI
7782-44-7
CAS
HMDB0001377
HMDB
PW064434
PathWhiz
C8H13N2O5P
Pyridoxamine 5'-phosphate
248.05621
C06055
KEGG Compound
C06054
KEGG Compound
2-Oxo-3-hydroxy-4-phosphobutanoic acid
SubPathwayOutput
Pyridoxamine 5'-phosphate
1.0
HMDB0001491
HMDB
SMILES
CC1=C(O)C(CO)=C(CO)C=N1
962
PubChem-compound
1050
PubChem-compound
1333-74-0
CAS
1051
PubChem-compound
Ammonia
1052
PubChem-compound
2-KETOGLUTARATE
BioCyc
RIBULOSE-5P
BioCyc
5800
ChemSpider
C00199
KEGG Compound
1.0
440901
PubChem-compound
1053
PubChem-compound
1.0
Phosphate
1054
PubChem-compound
Q96255
UniProt
1.0
1055
PubChem-compound
Pyridoxamine
SMILES
CC1=NC=C(CO)C(C=O)=C1O
SMILES
O=O
729
PubChem-compound
HMDB0000051
HMDB
Pyridoxal 5'-phosphate synthase subunit PDX1.1
1.0
HMDB0002111
HMDB
SMILES
N[C@@H](CCC(O)=O)C(O)=O
C4H9NO4
4-Hydroxy-L-threonine
135.05316
CHEBI:15377
ChEBI
C00647
KEGG Compound
Q9FZ62
UniProt
1.0
CHEBI:15379
ChEBI
14265-44-2
CAS
Chloroplast
C5H11O8P
D-Ribulose 5-phosphate
230.01915
CHEBI:18405
ChEBI
1.0
58-64-0
CAS
1.0
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
1.0
CHEBI:17310
ChEBI
HMDB0000618
HMDB
Phosphate
1.0
1.0
1.0
SMILES
CC1=NC=C(COP(O)(O)=O)C(CN)=C1O
1.0
4-Hydroxy-L-threonine
447-05-2
CAS
C00534
KEGG Compound
1.0
SMILES
N[C@@H](CCC(N)=O)C(O)=O
SMILES
OC(COP(O)(O)=O)C=O
PYRIDOXINE-5P
BioCyc
Pyridoxine
CHEBI:18050
ChEBI
H2O
Water
18.010565
Pyridoxamine 5'-phosphate
H2O2
Hydrogen peroxide
34.005478
Q9SSP5
UniProt
Pyridoxine 5'-phosphate
GAP
BioCyc
1061
PubChem-compound
977
PubChem-compound
1.0
C00661
KEGG Compound
SMILES
O[C@H](COP(O)(O)=O)C(=O)C(O)=O
SMILES
N[C@@H]([C@H](O)COP(O)(O)=O)C(O)=O
Q9LTX3
UniProt
HMDB0000641
HMDB
Hydrogen
SMILES
[H][H]