Structure of PDB 6r79 Chain D Binding Site BS01
Receptor Information
>6r79 Chain D (length=218) Species:
287
(Pseudomonas aeruginosa) [
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LPDLKIEKLEEGVFVHTSFEEVNGVVTKHGLVVLVNTDAYLIDTPFTATD
TEKLVNWFVERGYEIKGTISSHFHSDSTGGIEWLNSQSIPTYASELTNEL
LKKSGKVQAKYSFSEVSYWLVKNKIEVFYPGPGHTQDNLVVWLPESKILF
GGCFIKPHGLGNLGDANLEAWPKSAKILMSKYGKAKLVVSSHSEKGDASL
MKRTWEQALKGLKESKKT
Ligand information
Ligand ID
GLY
InChI
InChI=1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5)
InChIKey
DHMQDGOQFOQNFH-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C(=O)O)N
CACTVS 3.341
NCC(O)=O
ACDLabs 10.04
O=C(O)CN
Formula
C2 H5 N O2
Name
GLYCINE
ChEMBL
CHEMBL773
DrugBank
DB00145
ZINC
ZINC000004658552
PDB chain
6r79 Chain A Residue 311 [
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Receptor-Ligand Complex Structure
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PDB
6r79
Structure and Molecular Recognition Mechanism of IMP-13 Metallo-beta-Lactamase.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
V31 H197
Binding residue
(residue number reindexed from 1)
V26 H192
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H77 H79 D81 H139 C158 K161 N167 H197
Catalytic site (residue number reindexed from 1)
H72 H74 D76 H134 C153 K156 N162 H192
Enzyme Commision number
3.5.2.6
: beta-lactamase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008800
beta-lactamase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0017001
antibiotic catabolic process
GO:0046677
response to antibiotic
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:6r79
,
PDBe:6r79
,
PDBj:6r79
PDBsum
6r79
PubMed
32205343
UniProt
Q7WYA8
|BLAB_PSEAI Metallo-beta-lactamase type 2 (Gene Name=bla-imp13)
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