Structure of PDB 6d18 Chain A Binding Site BS03
Receptor Information
>6d18 Chain A (length=270) Species:
573
(Klebsiella pneumoniae) [
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HMLTNLVAEPFAKLEQDFGGSIGVYAMDTGSGATVSYRAEERFPLCSSFK
GFLAAAVLARSQQQAGLLDTPIRYGKNALVPWSPISEKYLTTGMTVAELS
AAAVQYSDNAAANLLLKELGGPAGLTAFMRSIGDTTFRLDRWELELNSAI
PGDARDTSSPRAVTESLQKLTLGSALAAPQRQQFVDWLKGNTTGNHRIRA
AVPADWAVGDKTGTCGVYGTANDYAVVWPTGRAPIVLAVYTRAPNKDDKH
SEAVIAAAARLALEGLGVNG
Ligand information
Ligand ID
GTV
InChI
InChI=1S/C12H13O5P/c1-7-3-8(2)12-9(6-18(14,15)16)5-11(13)17-10(12)4-7/h3-5H,6H2,1-2H3,(H2,14,15,16)
InChIKey
APYPWKQCSUQQTA-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1cc(C)c2C(=CC(=O)Oc2c1)C[P](O)(O)=O
ACDLabs 12.01
Cc2cc(C)c1C(CP(O)(O)=O)=CC(=O)Oc1c2
OpenEye OEToolkits 2.0.6
Cc1cc(c2c(c1)OC(=O)C=C2CP(=O)(O)O)C
Formula
C12 H13 O5 P
Name
[(5,7-dimethyl-2-oxo-2H-1-benzopyran-4-yl)methyl]phosphonic acid
ChEMBL
CHEMBL4545793
DrugBank
ZINC
ZINC000020760687
PDB chain
6d18 Chain A Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
6d18
Heteroaryl Phosphonates as Noncovalent Inhibitors of Both Serine- and Metallocarbapenemases.
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
R83 L142 G147 A150 F151
Binding residue
(residue number reindexed from 1)
R60 L119 G124 A127 F128
Annotation score
1
Binding affinity
MOAD
: Ki=1.4uM
PDBbind-CN
: -logKd/Ki=5.85,Ki=1.4uM
Enzymatic activity
Catalytic site (original residue number in PDB)
S70 K73 S130 E166 K234 T237
Catalytic site (residue number reindexed from 1)
S47 K50 S107 E143 K211 T214
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:6d18
,
PDBe:6d18
,
PDBj:6d18
PDBsum
6d18
PubMed
31483651
UniProt
Q9F663
|BLKPC_KLEPN Carbapenem-hydrolyzing beta-lactamase KPC (Gene Name=bla)
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