Structure of PDB 2h6a Chain A Binding Site BS01
Receptor Information
>2h6a Chain A (length=266) Species:
40324
(Stenotrophomonas maltophilia) [
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EVPLPQLRAYTVDASWLQPMAPLQIADHTWQIGTEDLTALLVQTPDGAVL
LDGGMPQMASHLLDNMKARGVTPRDLRLILLSHAHADHAGPVAELKRRTG
AKVAANAESAVLLARGGSDDLHFGDGITYPPANADRIVMDGEVITVGGIV
FTAHFMAGHTPGSTAWTWTDTRNGKPVRIAYADSLSAPGYQLQGNPRYPH
LIEDYRRSFATVRALPCDVLLTPHPGASNWDYAAGARAGAKALTCKAYAD
AAEQKFDGQLAKETAG
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2h6a Chain A Residue 320 [
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Receptor-Ligand Complex Structure
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PDB
2h6a
Structural insights into the design of inhibitors for the L1 metallo-beta-lactamase from Stenotrophomonas maltophilia.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
H116 H118 H196
Binding residue
(residue number reindexed from 1)
H83 H85 H159
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H116 H118 D120 H121 H196 Y229 H263
Catalytic site (residue number reindexed from 1)
H83 H85 D87 H88 H159 Y190 H224
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:0030655
beta-lactam antibiotic catabolic process
GO:0046677
response to antibiotic
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2h6a
,
PDBe:2h6a
,
PDBj:2h6a
PDBsum
2h6a
PubMed
17999929
UniProt
P52700
|BLA1_STEMA Metallo-beta-lactamase L1 type 3
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