9606
TAXONOMY
1.0
37768
PubChem-compound
Adenosine triphosphate
37517-28-5
CAS
AMP
BioCyc
C10H14N5O7P
Adenosine monophosphate
347.06308
Pyrophosphate
HMDB0000250
HMDB
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
P0A7K6
UniProt
14000-31-8
CAS
SubPathwayControl770
SubPathway770Control
InhibitorySubPathwayControl
HMDB0014622
HMDB
CHEBI:16027
ChEBI
Bacterial Ribosome
SubPathwayInhibition
HMDB0000538
HMDB
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
ATP
BioCyc
CHEBI:18361
ChEBI
C06820
KEGG Compound
C00002
KEGG Compound
1.0
1.0
SMILES
NCC[C@H](O)C(=O)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CN)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](N)[C@H]1O
559142
ChemSpider
Cytoplasm
SMP0000253
SMPDB
Amikacin
SubPathwayInhibitor
34635
ChemSpider
CHEBI:15422
ChEBI
644102
PubChem-compound
Reaction1959
false
Adenosine triphosphate → Adenosine monophosphate + Pyrophosphate
LEFT_TO_RIGHT
6083
PubChem-compound
Homo sapiens
5742
ChemSpider
C00013
KEGG Compound
61-19-8
CAS
Amikacin Action Pathway
SMILES
NC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1
O7P2
Pyrophosphate
173.91193
5957
PubChem-compound
Adenosine monophosphate
Amikacin inhibits Bacterial Ribosome
InhibitorySubPathway
CHEBI:2637
ChEBI
5858
ChemSpider
PW000351
PathWhiz
C10H16N5O13P3
Adenosine triphosphate
506.99576
56-65-5
CAS
C00020
KEGG Compound
Bacterial Ribosome
HMDB0000045
HMDB
C22H43N5O13
Amikacin
585.28577
GO:0005737
GENE ONTOLOGY
PPI
BioCyc