Structure of PDB 3juo Chain B Binding Site BS01
Receptor Information
>3juo Chain B (length=157) [
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ENTSENRAQVAARQHNRKIVEQYMHTRGEARLKRHLLFTEDGVGGLWTTD
SGQPIAIRGREKLGEHAVWSLQCFPDWVWTDIQIFETQDPNWFWVECRGE
GAIVFPGYPRGQYRNHFLHSFRFENGLIKEQREFMNPCEQFRSLGIEVPE
VRRDGLP
Ligand information
Ligand ID
AJD
InChI
InChI=1S/C12H15BrN2O2/c13-8-3-4-11(10(6-8)12(16)17)15-9-2-1-5-14-7-9/h3-4,6,9,14-15H,1-2,5,7H2,(H,16,17)/t9-/m1/s1
InChIKey
DFYNENBDVWMLFE-SECBINFHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1cc(c(cc1Br)C(=O)O)NC2CCCNC2
ACDLabs 11.02
O=C(O)c2c(NC1CCCNC1)ccc(Br)c2
CACTVS 3.352
OC(=O)c1cc(Br)ccc1N[CH]2CCCNC2
OpenEye OEToolkits 1.7.0
c1cc(c(cc1Br)C(=O)O)N[C@@H]2CCCNC2
CACTVS 3.352
OC(=O)c1cc(Br)ccc1N[C@@H]2CCCNC2
Formula
C12 H15 Br N2 O2
Name
5-bromo-2-[(3R)-piperidin-3-ylamino]benzoic acid
ChEMBL
DrugBank
ZINC
ZINC000058632126
PDB chain
3juo Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
3juo
The Active Site of an Enzyme Can Host Both Enantiomers of a Racemic Ligand Simultaneously
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
R38 R41 H73 A74 S77 F81 W84 E140
Binding residue
(residue number reindexed from 1)
R31 R34 H66 A67 S70 F74 W77 E133
Annotation score
1
Binding affinity
MOAD
: Kd=8.55uM
PDBbind-CN
: -logKd/Ki=5.07,Kd=8.55uM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0017000
antibiotic biosynthetic process
View graph for
Biological Process
External links
PDB
RCSB:3juo
,
PDBe:3juo
,
PDBj:3juo
PDBsum
3juo
PubMed
19876985
UniProt
Q396C9
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