Structure of PDB 1ny0 Chain A Binding Site BS01
Receptor Information
>1ny0 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
]
HPETLVKVKDAEDQLGARVGYIELDLNSGKILESFRPEERFPMMSTFKVL
LCGAVLSRVDAGQEQLGRRIHYSQNDLVEYSPVTEKHLTDGMTVRELCSA
AITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRWEPELNEAIPN
DERDTTTPAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSAL
PAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNR
QIAEIGASLIKHW
Ligand information
Ligand ID
NBF
InChI
InChI=1S/C14H16BNO4/c1-2-20-12-8-7-10-5-3-4-6-11(10)13(12)14(17)16-9-15(18)19/h3-8,18-19H,2,9H2,1H3,(H,16,17)
InChIKey
VGXJNGVFESCMME-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
CCOc1ccc2ccccc2c1C(=O)NCB(O)O
OpenEye OEToolkits 1.5.0
B(CNC(=O)c1c2ccccc2ccc1OCC)(O)O
ACDLabs 10.04
O=C(c1c2c(ccc1OCC)cccc2)NCB(O)O
Formula
C14 H16 B N O4
Name
[(2-ETHOXY-1-NAPHTHOYL)AMINO]METHYLBORONIC ACID
ChEMBL
CHEMBL1234635
DrugBank
DB02841
ZINC
ZINC000169748477
PDB chain
1ny0 Chain A Residue 300 [
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
1ny0
Recognition and Resistance in TEM beta-lactamase
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
S70 K73 Y105 S130 N132 N170 G236 A237 G238 E240
Binding residue
(residue number reindexed from 1)
S45 K48 Y80 S105 N107 N145 G211 A212 G213 E214
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=5.85,Ki=1.4uM
Enzymatic activity
Catalytic site (original residue number in PDB)
S70 K73 S130 E166 K234 A237
Catalytic site (residue number reindexed from 1)
S45 K48 S105 E141 K209 A212
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
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:1ny0
,
PDBe:1ny0
,
PDBj:1ny0
PDBsum
1ny0
PubMed
12859188
UniProt
P62593
|BLAT_ECOLX Beta-lactamase TEM (Gene Name=bla)
[
Back to BioLiP
]