Structure of PDB 6ooh Chain A Binding Site BS02
Receptor Information
>6ooh Chain A (length=263) Species:
562
(Escherichia coli) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
PTSAVQQKLAALEKSSGGRLGVALIDTADNTQVLYRGDERFPMCSTSKVM
AAAAVLKQSETQKQLLNQPVEIKHADLVNYNPIAEKHVNGTMTLAELSAA
ALQYSDNTAMNKLIAQLGGPGGVTAFARAIGDETFRLDRTEPTLNTAIPG
DPRDTTTPRAMAQTLRQLTLGHALGETQRAQLVTWLKGNTTGAASIRAGL
PTSWTVGDKTGSGGYGTTNDIAVIWPQGRAPLVLVTYFTQPQQNAESRRD
VLASAARIIAEGL
Ligand information
Ligand ID
J1X
InChI
InChI=1S/C18H12F3N7O/c19-18(20,21)13-7-12(9-15(10-13)28-6-2-5-22-28)17(29)23-14-4-1-3-11(8-14)16-24-26-27-25-16/h1-10H,(H,23,29)(H,24,25,26,27)
InChIKey
ZMYXPNSTNVZUGF-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
FC(F)(F)c1cc(cc(c1)C(=O)Nc2cccc(c2)c3[nH]nnn3)n4cccn4
ACDLabs 12.01
C(=O)(c1cc(C(F)(F)F)cc(c1)n2cccn2)Nc3cccc(c3)c4nnnn4
OpenEye OEToolkits 2.0.7
c1cc(cc(c1)NC(=O)c2cc(cc(c2)n3cccn3)C(F)(F)F)c4[nH]nnn4
Formula
C18 H12 F3 N7 O
Name
3-(1H-pyrazol-1-yl)-N-[3-(1H-tetrazol-5-yl)phenyl]-5-(trifluoromethyl)benzamide
ChEMBL
DrugBank
ZINC
PDB chain
6ooh Chain A Residue 302 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
6ooh
An Empirical Study of Amide-Heteroarene pi-Stacking Interactions Using Reversible Inhibitors of a Bacterial Serine Hydrolase.
Resolution
1.499 Å
Binding residue
(original residue number in PDB)
N104 Y105 T216 S237 S274 R276
Binding residue
(residue number reindexed from 1)
N79 Y80 T191 S212 S247 R249
Annotation score
1
Binding affinity
MOAD
: Kd=2.19uM
Enzymatic activity
Catalytic site (original residue number in PDB)
S70 K73 S130 E166 K234 S237
Catalytic site (residue number reindexed from 1)
S45 K48 S105 E141 K209 S212
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6ooh
,
PDBe:6ooh
,
PDBj:6ooh
PDBsum
6ooh
PubMed
32774871
UniProt
I7AP60
[
Back to BioLiP
]