9606
TAXONOMY
1.0
Adenosine triphosphate
SMILES
CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]2NC(N)=N)O[C@@H](C)[C@]1(O)C=O
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
19649
PubChem-compound
CHEBI:16027
ChEBI
Bacterial Ribosome
SubPathwayInhibition
SMP0000259
SMPDB
HMDB0000538
HMDB
CHEBI:17076
ChEBI
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
SubPathwayControl778
SubPathway778Control
InhibitorySubPathwayControl
ATP
BioCyc
CHEBI:18361
ChEBI
C00002
KEGG Compound
1.0
1.0
559142
ChemSpider
Cytoplasm
Streptomycin inhibits Bacterial Ribosome
InhibitorySubPathway
C00413
KEGG Compound
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
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
C21H39N7O12
Streptomycin
581.2657
5957
PubChem-compound
Adenosine monophosphate
18508
ChemSpider
Streptomycin Action Pathway
5858
ChemSpider
HMDB0015214
HMDB
C10H16N5O13P3
Adenosine triphosphate
506.99576
PW000357
PathWhiz
57-92-1
CAS
Streptomycin
SubPathwayInhibitor
56-65-5
CAS
C00020
KEGG Compound
Bacterial Ribosome
HMDB0000045
HMDB
GO:0005737
GENE ONTOLOGY
PPI
BioCyc