Structure of PDB 4lv0 Chain B Binding Site BS01
Receptor Information
>4lv0 Chain B (length=358) Species:
83333
(Escherichia coli K-12) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
APQQINDIVHRTITPLIEQQKIPGMAVAVIYQGKPYYFTWGYADIAKKQP
VTQQTLFELGSVSKTFTGVLGGDAIARGEIKLSDPTTKYWPELTAKQWNG
ITLLHLATYTAGGLPLQVPDEVKSSSDLLRFYQNWQPAWAPGTQRLYANS
SIGLFGALAVKPSGLSFEQAMQTRVFQPLKLNHTWINVPPAEEKNYAWGY
REGKAVHVSPGALDAEAYGVKSTIEDMARWVQSNLKPLDINEKTLQQGIQ
LAQSRYWQTGDMYQGLGWEMLDWPVNPDSIINGSDNKIALAARPVKAITP
PTPAVRASWVHKTGATGGFGSYVAFIPEKELGIVMLANKNYPNPARVDAA
WQILNALQ
Ligand information
Ligand ID
APB
InChI
InChI=1S/C6H8BNO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H,8H2
InChIKey
JMZFEHDNIAQMNB-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Nc1cccc(c1)B(O)O
OpenEye OEToolkits 1.5.0
B(c1cccc(c1)N)(O)O
ACDLabs 10.04
OB(O)c1cccc(N)c1
Formula
C6 H8 B N O2
Name
M-AMINOPHENYLBORONIC ACID
ChEMBL
CHEMBL20852
DrugBank
DB01896
ZINC
ZINC000169743006
PDB chain
4lv0 Chain B Residue 401 [
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
4lv0
Covalent docking of large libraries for the discovery of chemical probes.
Resolution
1.652 Å
Binding residue
(original residue number in PDB)
S64 Y150 N152 Y221 A318
Binding residue
(residue number reindexed from 1)
S61 Y147 N149 Y218 A315
Annotation score
1
Binding affinity
BindingDB: Ki=7300nM
Enzymatic activity
Catalytic site (original residue number in PDB)
S64 K67 Y112 A114 V121 Y150 G156 E272 K315 A318
Catalytic site (residue number reindexed from 1)
S61 K64 Y109 A111 V118 Y147 G153 E269 K312 A315
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:0046677
response to antibiotic
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0042597
periplasmic space
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4lv0
,
PDBe:4lv0
,
PDBj:4lv0
PDBsum
4lv0
PubMed
25344815
UniProt
P00811
|AMPC_ECOLI Beta-lactamase (Gene Name=ampC)
[
Back to BioLiP
]