47205727
PubChem-compound
47205726
PubChem-compound
47205725
PubChem-compound
6022
PubChem-compound
647
PubChem-compound
1.0
ReactionCatalysis202877
ACTIVATION
ReactionCatalysis202876
ACTIVATION
3702
TAXONOMY
ReactionCatalysis202873
ACTIVATION
ReactionCatalysis202872
ACTIVATION
937
ChemSpider
ReactionCatalysis202875
ACTIVATION
ReactionCatalysis202874
ACTIVATION
C03024
KEGG Compound
ReactionCatalysis202871
ACTIVATION
C15H24N5O13P3
Isopentenyl-ATP
575.05835
AMP
BioCyc
tRNA adenine
C15H24N5O14P3
trans-Zeatin riboside triphosphate
591.0533
C15H23N5O10P2
Isopentenyladenosine-5'-diphosphate
495.092
C04083
KEGG Compound
SMILES
O
Isopentenyl-AMP
tRNA adenine
47205723
PubChem-compound
C10H14N5O7P
Adenosine monophosphate
347.06308
47205722
PubChem-compound
trans-Zeatin riboside diphosphate
N6-dimethylallyladenine
1.0
HMDB0001341
HMDB
1.0
CHEBI:71938
ChEBI
CHEBI:16027
ChEBI
1.0
1.0
1.0
HMDB0000538
HMDB
ATP
BioCyc
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
1.0
C15H23N5O11P2
trans-Zeatin riboside diphosphate
511.08694
C15H22N5O7P
Isopentenyl-AMP
415.12567
C15H22N5O8P
trans-Zeatin riboside monophosphate
431.1206
C03161
KEGG Compound
2365-40-4
CAS
1.0
ADP
BioCyc
92180
PubChem-compound
Cytokinin hydroxylase
CHEBI:15422
ChEBI
SMP0121210
SMPDB
358-72-5
CAS
5742
ChemSpider
SubPathwayInteraction113050
SubPathwayReaction
SubPathway113050Reaction
Arabidopsis thaliana
7732-18-5
CAS
1.0
Adenylate isopentenyltransferase 1, chloroplastic
952
ChemSpider
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
Isopentenyl-ATP
O2
Oxygen
31.98983
CHEBI:81008
ChEBI
GO:0009507
GENE ONTOLOGY
Isopentenyladenosine-5'-diphosphate
CPD-4209
BioCyc
SMILES
OP(O)(=O)OP(O)(O)=O
HMDB0001120
HMDB
trans-Zeatin riboside triphosphate
CHEBI:15819
ChEBI
5858
ChemSpider
CPD-4211
BioCyc
CHEBI:71719
ChEBI
C10H16N5O13P3
Adenosine triphosphate
506.99576
CHEBI:71679
ChEBI
[Reduced NADPH---hemoprotein reductase]
[Oxidized NADPH---hemoprotein reductase]
CHEBI:71678
ChEBI
CHEBI:16761
ChEBI
1023
PubChem-compound
7782-44-7
CAS
HMDB0001377
HMDB
Oxygen
HMDB0000045
HMDB
Dimethylallylpyrophosphate
SubPathwayOutput
SMILES
CC(C)=CCNC1=NC=NC2=C1N=CN2
962
PubChem-compound
1.0
[Reduced NADPH---hemoprotein reductase]
83222
ChemSpider
5800
ChemSpider
1.0
Adenosine monophosphate
[Oxidized NADPH---hemoprotein reductase]
C04713
KEGG Compound
CPD-6641
BioCyc
C00235
KEGG Compound
CHEBI:16057
ChEBI
CHEBI:17660
ChEBI
Terpenoid Backbone Biosynthesis
SubPathway
SMILES
O=O
Adenosine triphosphate
SMP0122765
SMPDB
H4O7P2
Diphosphoric acid
177.94322
HMDB0002111
HMDB
CHEBI:15377
ChEBI
C00008
KEGG Compound
C00007
KEGG Compound
CHEBI:15379
ChEBI
C16430
KEGG Compound
Chloroplast
C5H12O7P2
Dimethylallylpyrophosphate
246.00583
58-64-0
CAS
C00001
KEGG Compound
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
Diphosphoric acid
1.0
tRNA dimethylallyltransferase
PW122504
PathWhiz
1.0
C00002
KEGG Compound
CHEBI:29888
ChEBI
C16429
KEGG Compound
C10H13N5
N6-dimethylallyladenine
203.1171
C16426
KEGG Compound
C16428
KEGG Compound
tRNA dimethylallyltransferase
PW124096
PathWhiz
C16424
KEGG Compound
Zeatin Biosynthesis
1.0
6083
PubChem-compound
2466-09-3
CAS
2.5.1.112,2.5.1.27
false
2.5.1.112,2.5.1.27
Adenosine triphosphate + Dimethylallylpyrophosphate → Diphosphoric acid + Isopentenyl-ATP
LEFT_TO_RIGHT
1.14.13.-
false
1.14.13.-
Isopentenyl-ATP + Oxygen + [Reduced NADPH---hemoprotein reductase] → Water + [Oxidized NADPH---hemoprotein reductase] + trans-Zeatin riboside triphosphate
LEFT_TO_RIGHT
2.5.1.112
false
2.5.1.112
Adenosine diphosphate + Dimethylallylpyrophosphate → Diphosphoric acid + Isopentenyladenosine-5'-diphosphate
LEFT_TO_RIGHT
Reaction213286
false
Dimethylallylpyrophosphate + tRNA adenine → Diphosphoric acid + N6-dimethylallyladenine
LEFT_TO_RIGHT
1.14.13.-
false
1.14.13.-
Isopentenyladenosine-5'-diphosphate + Oxygen + [Reduced NADPH---hemoprotein reductase] → Water + [Oxidized NADPH---hemoprotein reductase] + trans-Zeatin riboside diphosphate
LEFT_TO_RIGHT
2.5.1.27
false
2.5.1.27
Adenosine monophosphate + Dimethylallylpyrophosphate → Diphosphoric acid + Isopentenyl-AMP
LEFT_TO_RIGHT
1.0
Adenosine diphosphate
1.14.13.-
false
1.14.13.-
Isopentenyl-AMP + Oxygen + [Reduced NADPH---hemoprotein reductase] → Water + [Oxidized NADPH---hemoprotein reductase] + trans-Zeatin riboside monophosphate
LEFT_TO_RIGHT
C00013
KEGG Compound
SMILES
CC(C)=CCNC1=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
H2O
Water
18.010565
SMILES
C\C(CO)=C/CNC1=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
SMILES
CC(C)=CCNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
5957
PubChem-compound
Q9ZUX7
UniProt
977
PubChem-compound
7285
PubChem-compound
trans-Zeatin riboside monophosphate
56-65-5
CAS
CHEBI:71875
ChEBI
627
ChemSpider
SMILES
CC(C)=CCO[P@](O)(=O)OP(O)(O)=O
C00020
KEGG Compound
SMILES
C\C(CO)=C/CNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O
1.0
C10H15N5O10P2
Adenosine diphosphate
427.02942
Water
1.0
SMILES
C\C(CO)=C/CNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
SMILES
CC(C)=CCNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O