Structure of PDB 3u9f Chain A Binding Site BS01
Receptor Information
>3u9f Chain A (length=215) Species:
562
(Escherichia coli) [
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EKKITGYTTVDISQWHRKEHFEAFQSVAQCTYNQTVQLDITAFLKTVKKN
KHKFYPAFIHILARLMNAHPEFRMAMKDGELVIWDSVHPCYTVFHEQTET
FSSLWSEYHDDFRQFLHIYSQDVACYGENLAYFPKGFIENMFFVSANPWV
SFTSFDLNVANMDNFFAPVFTMGKYYTQGDKVLMPLAIQVHHAVCDGFHV
GRMLNELQQYCDEWQ
Ligand information
Ligand ID
CLM
InChI
InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)/t8-,9-/m1/s1
InChIKey
WIIZWVCIJKGZOK-RKDXNWHRSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(ccc1C(C(CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
CACTVS 3.341
OC[CH](NC(=O)C(Cl)Cl)[CH](O)c1ccc(cc1)[N+]([O-])=O
OpenEye OEToolkits 1.5.0
c1cc(ccc1[C@H]([C@@H](CO)NC(=O)C(Cl)Cl)O)[N+](=O)[O-]
CACTVS 3.341
OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+]([O-])=O
ACDLabs 10.04
ClC(Cl)C(=O)NC(C(O)c1ccc([N+]([O-])=O)cc1)CO
Formula
C11 H12 Cl2 N2 O5
Name
CHLORAMPHENICOL
ChEMBL
CHEMBL130
DrugBank
DB00446
ZINC
ZINC000000113382
PDB chain
3u9f Chain A Residue 221 [
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Receptor-Ligand Complex Structure
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PDB
3u9f
The structural basis for substrate versatility of chloramphenicol acetyltransferase CAT(I).
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
S104 Y133 S146 F166
Binding residue
(residue number reindexed from 1)
S103 Y132 S145 F165
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
R18 T172 H193 D197
Catalytic site (residue number reindexed from 1)
R17 T171 H192 D196
Enzyme Commision number
2.3.1.28
: chloramphenicol O-acetyltransferase.
Gene Ontology
Molecular Function
GO:0008811
chloramphenicol O-acetyltransferase activity
GO:0016746
acyltransferase activity
Biological Process
GO:0046677
response to antibiotic
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3u9f
,
PDBe:3u9f
,
PDBj:3u9f
PDBsum
3u9f
PubMed
22294317
UniProt
P62577
|CAT_ECOLX Chloramphenicol acetyltransferase (Gene Name=cat)
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