9606
TAXONOMY
1.0
HMDB0014897
HMDB
SubPathwayControl783
InhibitorySubPathwayControl
SubPathway783Control
CHEBI:27902
ChEBI
Adenosine triphosphate
AMP
BioCyc
SMILES
[H][C@@]12C[C@@]3([H])C(=C(O)[C@]1(O)C(=O)C(C(N)=O)=C(O)[C@H]2N(C)C)C(=O)C1=C(O)C=CC=C1[C@@]3(C)O
C10H14N5O7P
Adenosine monophosphate
347.06308
Pyrophosphate
HMDB0000250
HMDB
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
P0A7K6
UniProt
14000-31-8
CAS
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
Tetracycline
SubPathwayInhibitor
C00002
KEGG Compound
1.0
1.0
559142
ChemSpider
Cytoplasm
SMP0000294
SMPDB
PW000362
PathWhiz
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
C22H24N2O8
Tetracycline
444.15326
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
Tetracycline Action Pathway
5957
PubChem-compound
Adenosine monophosphate
5858
ChemSpider
C10H16N5O13P3
Adenosine triphosphate
506.99576
56-65-5
CAS
C00020
KEGG Compound
Bacterial Ribosome
HMDB0000045
HMDB
C06570
KEGG Compound
GO:0005737
GENE ONTOLOGY
PPI
BioCyc
Tetracycline inhibits Bacterial Ribosome
InhibitorySubPathway
10257122
ChemSpider
60-54-8
CAS