Cyclic pyranopterin monophosphate
CHEBI:71308
ChEBI
SMILES
NC1=NC(=O)C2=C(NCC(=N2)C(O)C(O)CO)N1
937
ChemSpider
1.0
Molybdate
Molybdopterin synthase sulfur carrier subunit
GTP cyclohydrolase 1
Molybdopterin synthase catalytic subunit
1.0
Cytidine triphosphate
SMILES
O
26332851
ChemSpider
C19848
KEGG Compound
Pyrophosphate
C10H14N5O7P
Adenosine monophosphate
347.06308
ReactionCatalysis5127
ACTIVATION
1.0
ReactionCatalysis5125
ACTIVATION
HMDB0002275
HMDB
ReactionCatalysis5126
ACTIVATION
CHEBI:16027
ChEBI
4883416
ChemSpider
Adenylyl-molybdopterin
SMILES
[H]C12NC3=C(NC1([H])C1=C(S[Mo](=O)(=O)S1)C(COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1O)N1C=CC(N)=NC1=O)O2)C(=O)NC(N)=N3
C9H12N5O7P
7,8-dihydroneopterin 3'-phosphate
333.04742
HMDB0000538
HMDB
C9H12N5O13P3
7,8-dihydroneopterin 3'-triphosphate
490.96664
DIHYDROXYPHENYLGLYCOLALDEHYDE
BioCyc
ATP
BioCyc
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
1.0
Molybdopterin
Molybdopterin adenylyltransferase
559142
ChemSpider
Endocytosis
SubPathway
Dihydroneopterin triphosphate pyrophosphatase
C10H12MoN5O8PS2
Molybdopterin
522.8919
C20H26N10O12P2S2
Adenylyl-molybdopterin
724.0648
(2-amino-4-hydroxy-7,8-dihydropteridin-6-yl)methyl diphosphate
6-hydroxymethyl-7,8-dihydropterin
1.0
5742
ChemSpider
1038
PubChem-compound
Uncharacterized protein ygfJ
278
ChemSpider
CHEBI:62728
ChEBI
Adenosine monophosphate
25245170
PubChem-compound
1.0
2.7.7.76
false
2.7.7.76
Cytidine triphosphate + Hydrogen Ion + molybdenum cofactor → Cytidylyl molybdenum cofactor + Pyrophosphate
LEFT_TO_RIGHT
C10H14N5O8P
Cyclic pyranopterin monophosphate
363.058
5858
ChemSpider
O4P
Phosphate
94.95342
Molybdopterin molybdenumtransferase
6830
PubChem-compound
1010
ChemSpider
DIHYDRONEOPTERIN-P3
BioCyc
1.0
PPI
BioCyc
Molybdenum cofactor biosynthesis protein A
ReactionCatalysis5952
ACTIVATION
1.0
C10H16N5O14P3
Guanosine triphosphate
522.99066
C05924
KEGG Compound
Hydrogen Ion
23304237
PubChem-compound
1.0
Adenosine triphosphate
Molybdopterin synthase sulfur carrier subunit
SMILES
[O-]P([O-])([O-])=O
1.0
CHEBI:2137
ChEBI
Formic acid
C00009
KEGG Compound
C00001
KEGG Compound
HMDB0001429
HMDB
17221217
ChemSpider
CTP
BioCyc
CHEBI:18361
ChEBI
CHEBI:18367
ChEBI
141-46-8
CAS
molybdenum cofactor
1032
ChemSpider
GTP cyclohydrolase 1
C00002
KEGG Compound
Molybdopterin synthase catalytic subunit
Dihydroneopterin triphosphate pyrophosphatase
Glycolaldehyde
C06232
KEGG Compound
46173482
PubChem-compound
C2H4O2
Glycolaldehyde
60.02113
2.0
thiocarboxylated small subunit of molybdopterin synthase
GTP cyclohydrolase I
P26281
UniProt
C10H18MoN5O8PS2
molybdenum cofactor
528.93884
7782-91-4
CAS
molybdopterin synthase
molybdopterin adenylyltransferase
7,8-dihydroneopterin 3'-triphosphate
Molybdopterin adenylyltransferase
HMDB0059628
HMDB
C00013
KEGG Compound
7,8-dihydroneopterin 3'-phosphate
CHEBI:17001
ChEBI
2.0
Uncharacterized protein ygfJ
O7P2
Pyrophosphate
173.91193
3.0
dihydroneopterin aldolase
ReactionCatalysis5904
ACTIVATION
1.0
5957
PubChem-compound
C9H16N3O14P3
Cytidine triphosphate
482.9845
562
TAXONOMY
Dihydroneopterin aldolase
H
Hydrogen Ion
1.007825
CHEBI:15996
ChEBI
P0AC16
UniProt
GTP Degradation and Molybdenum Cofactor Biosynthesis
H2MoO4
Molybdate
163.89961
56-65-5
CAS
C00020
KEGG Compound
HMDB0059639
HMDB
Guanosine triphosphate
SubPathwayOutput
C00266
KEGG Compound
Molybdenum cofactor biosynthesis protein A
1.0
CPD0-1882
BioCyc
Cytidylyl molybdenum cofactor
P0AF03
UniProt
CPD-8587
BioCyc
C04874
KEGG Compound
73508-07-3
CAS
4.1.2.25
false
4.1.2.25
7,8-Dihydroneopterin → 6-hydroxymethyl-7,8-dihydropterin + Glycolaldehyde
LEFT_TO_RIGHT
Reaction3398
false
7,8-dihydroneopterin 3'-phosphate + Water → 7,8-Dihydroneopterin + Phosphate
LEFT_TO_RIGHT
Water
3.6.1.-
false
3.6.1.-
7,8-dihydroneopterin 3'-triphosphate + Water → 7,8-dihydroneopterin 3'-phosphate + Hydrogen Ion + Pyrophosphate
LEFT_TO_RIGHT
AMP
BioCyc
3.5.4.16
false
3.5.4.16
Guanosine triphosphate + Water → 7,8-dihydroneopterin 3'-triphosphate + Formic acid + Hydrogen Ion
LEFT_TO_RIGHT
CHEBI:25371
ChEBI
SMILES
NC1=NC(=O)N(C=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
HMDB0000250
HMDB
SMILES
[H][C@@]12COP(O)(=O)O[C@]1([H])C(O)(O)[C@]1([H])NC3=C(NC(=N)N=C3O)N[C@]1([H])O2
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
C18239
KEGG Compound
14000-31-8
CAS
SMP0001902
SMPDB
1218-98-0
CAS
CHEBI:21437
ChEBI
756
PubChem-compound
C00044
KEGG Compound
7,8-Dihydroneopterin
SMILES
O[Mo++](O)(=O)=O
1.0
CHEBI:17071
ChEBI
HMDB0002206
HMDB
18971002
PubChem-compound
2.0
HMDB0000142
HMDB
CHEBI:15422
ChEBI
Escherichia coli
P30745
UniProt
7732-18-5
CAS
C00058
KEGG Compound
P30749
UniProt
P30748
UniProt
61-19-8
CAS
SMILES
NC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1
CH2O2
Formic acid
46.005478
Dihydroneopterin aldolase
C00063
KEGG Compound
molybdopterin molybdenumtransferase
ReactionCatalysis3364
ACTIVATION
FORMATE
BioCyc
PW001888
PathWhiz
10.0
ReactionCatalysis3367
ACTIVATION
4.0
ReactionCatalysis3365
ACTIVATION
ReactionCatalysis3366
ACTIVATION
SMILES
NC1=NC2=C(N=C(CO)CN2)C(=O)N1
1.0
SMILES
OP(=O)(OCC1=NC2=C(NC1)NC(=N)N=C2[O-])OP([O-])([O-])=O
C19H24MoN8O15P2S2
Cytidylyl molybdenum cofactor
827.93317
C10H16N5O13P3
Adenosine triphosphate
506.99576
1.0
659
PubChem-compound
53356705
PubChem-compound
HMDB0012260
HMDB
P0AFC0
UniProt
8.0
HMDB0000045
HMDB
65-47-4
CAS
P0A6T5
UniProt
25201779
PubChem-compound
SMILES
NC1=NC2=C(NC3C(N2)OC(COP(O)(O)=O)C2=C3S[Mo](=O)(=O)S2)C(=O)N1
962
PubChem-compound
SMILES
O.O.[Mo++].OC1=NC(=N)NC2=C1NC1C(N2)OC(COP(O)(O)=O)C(S)=C1S
SubPathwayInteraction112380
SubPathway112380Reaction
SubPathwayReaction
736
ChemSpider
Phosphate
1.0
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
2.0
C00080
KEGG Compound
CHEBI:30751
ChEBI
1.0
HMDB0002111
HMDB
SMILES
OC=O
CHEBI:15377
ChEBI
CHEBI:17677
ChEBI
CHEBI:15378
ChEBI
SMILES
[H+]
14265-44-2
CAS
C7H8N5O8P2
(2-amino-4-hydroxy-7,8-dihydropteridin-6-yl)methyl diphosphate
351.9848
6176
PubChem-compound
C7H9N5O2
6-hydroxymethyl-7,8-dihydropterin
195.07562
74188
ChemSpider
6569
ChemSpider
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
GTP
BioCyc
1.0
1.0
CHEBI:57602
ChEBI
CHEBI:60210
ChEBI
HMDB0001273
HMDB
644102
PubChem-compound
thiocarboxylated small subunit of molybdopterin synthase
5941
ChemSpider
6083
PubChem-compound
SMILES
NC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O)C(=O)N1
639
ChemSpider
Q46810
UniProt
64-18-6
CAS
C9H13N5O4
7,8-Dihydroneopterin
255.09676
1.0
1.0
H2O
Water
18.010565
CHEBI:17083
ChEBI
Molybdopterin molybdenumtransferase
4.1.99.18
false
4.1.99.18
Guanosine triphosphate → Cyclic pyranopterin monophosphate + Pyrophosphate
LEFT_TO_RIGHT
2.8.1.12
false
2.8.1.12
Cyclic pyranopterin monophosphate + Water + thiocarboxylated small subunit of molybdopterin synthase → 4 Hydrogen Ion + Molybdopterin + 2 thiocarboxylated small subunit of molybdopterin synthase
LEFT_TO_RIGHT
2.7.7.75
false
2.7.7.75
Adenosine triphosphate + Hydrogen Ion + Molybdopterin → Adenylyl-molybdopterin + Pyrophosphate
LEFT_TO_RIGHT
86-01-1
CAS
HMDB0003344
HMDB
1061
PubChem-compound
SMILES
NC1=NC(=O)C2=C(NCC(=N2)C(O)C(O)COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)N1
HMDB0059597
HMDB
SMILES
[H][C@@](O)(COP(O)([O-])=O)[C@@]([H])(O)C1=NC2=C(NC1)NC(=N)N=C2[O-]
16061579
PubChem-compound
2.10.1.1
false
2.10.1.1
Adenylyl-molybdopterin + Hydrogen Ion + Molybdate → Adenosine monophosphate + Water + molybdenum cofactor
LEFT_TO_RIGHT
SMILES
OCC=O
1.0
HMDB0000082
HMDB
SMILES
[H][C@]1(COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)O[C@@]2([H])NC3=C(N[C@@]2([H])C(S)=C1S)C(=O)N=C(N)N3
2.7.6.3
false
2.7.6.3
6-hydroxymethyl-7,8-dihydropterin + Adenosine triphosphate → (2-amino-4-hydroxy-7,8-dihydropteridin-6-yl)methyl diphosphate + Adenosine monophosphate + Hydrogen Ion
LEFT_TO_RIGHT
P12281
UniProt
82208
PubChem-compound