Structure of PDB 2hdu Chain A Binding Site BS02
Receptor Information
>2hdu Chain A (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
F12
InChI
InChI=1S/C7H7NO3S/c1-4(9)8-6-5(7(10)11)2-3-12-6/h2-3H,1H3,(H,8,9)(H,10,11)
InChIKey
RCEBHKDQZCVBTC-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)c1c(scc1)NC(=O)C
CACTVS 3.341
CC(=O)Nc1sccc1C(O)=O
OpenEye OEToolkits 1.5.0
CC(=O)Nc1c(ccs1)C(=O)O
Formula
C7 H7 N O3 S
Name
2-(ACETYLAMINO)THIOPHENE-3-CARBOXYLIC ACID
ChEMBL
CHEMBL1213612
DrugBank
ZINC
ZINC000001389744
PDB chain
2hdu Chain A Residue 1009 [
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
2hdu
Deconstructing fragment-based inhibitor discovery
Resolution
1.49 Å
Binding residue
(original residue number in PDB)
Y221 A318 T319 G320 N343
Binding residue
(residue number reindexed from 1)
Y218 A315 T316 G317 N340
Annotation score
1
Binding affinity
MOAD
: Ki=5mM
BindingDB: Ki=5000000nM
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:2hdu
,
PDBe:2hdu
,
PDBj:2hdu
PDBsum
2hdu
PubMed
17072304
UniProt
P00811
|AMPC_ECOLI Beta-lactamase (Gene Name=ampC)
[
Back to BioLiP
]