Structure of PDB 4de2 Chain B Binding Site BS01
Receptor Information
>4de2 Chain B (length=261) Species:
562
(Escherichia coli) [
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SAVQQKLAALEKSSGGRLGVALIDTADNTQVLYRGDERFPMCSTSKVMAA
AAVLKQSETQKQLLNQPVEIKPADLVNYNPIAEKHVNGTMTLAELSAAAL
QYSDNTAMNKLIAQLGGPGGVTAFARAIGDETFRLDRTEPTLNTAIPGDP
RDTTTPRAMAQTLRQLTLGHALGETQRAQLVTWLKGNTTGAASIRAGLPT
SWTAGDKTGSGDYGTTNDIAVIWPQGRAPLVLVTYFTQPQQNAESRRDVL
ASAARIIAEGL
Ligand information
Ligand ID
DN3
InChI
InChI=1S/C17H18N6O/c1-23(2)11-12-5-3-7-14(9-12)17(24)18-15-8-4-6-13(10-15)16-19-21-22-20-16/h3-10H,11H2,1-2H3,(H,18,24)(H,19,20,21,22)
InChIKey
YNFKRUNLXWQDEZ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
OpenEye OEToolkits 1.7.6
CN(C)Cc1cccc(c1)C(=O)Nc2cccc(c2)c3[nH]nnn3
ACDLabs 12.01
O=C(c1cccc(c1)CN(C)C)Nc2cccc(c2)c3nnnn3
Formula
C17 H18 N6 O
Name
3-[(dimethylamino)methyl]-N-[3-(1H-tetrazol-5-yl)phenyl]benzamide
ChEMBL
CHEMBL2031553
DrugBank
ZINC
PDB chain
4de2 Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4de2
Structure-Based Design of Potent and Ligand-Efficient Inhibitors of CTX-M Class A Beta-Lactamase
Resolution
1.4 Å
Binding residue
(original residue number in PDB)
I155 G156 Q192 G196 H197 A198
Binding residue
(residue number reindexed from 1)
I128 G129 Q165 G169 H170 A171
Annotation score
1
Binding affinity
MOAD
: Ki=76uM
Enzymatic activity
Catalytic site (original residue number in PDB)
S70 K73 S130 E166 K234 S237
Catalytic site (residue number reindexed from 1)
S43 K46 S103 E139 K207 S210
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008800
beta-lactamase activity
GO:0016787
hydrolase activity
Biological Process
GO:0017001
antibiotic catabolic process
GO:0030655
beta-lactam antibiotic catabolic process
GO:0046677
response to antibiotic
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Molecular Function
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Biological Process
External links
PDB
RCSB:4de2
,
PDBe:4de2
,
PDBj:4de2
PDBsum
4de2
PubMed
22296601
UniProt
Q9L5C8
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