Structure of PDB 6rz0 Chain A Binding Site BS02
Receptor Information
>6rz0 Chain A (length=251) Species:
83333
(Escherichia coli K-12) [
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MNLNSIPAFDDNYIWVLNDEAGRCLIVDPGDAEPVLNAIAANNWQPEAIF
LTHHHHDHVGGVKELVEKFPQIVVYGPQETQDKGTTQVVKDGETAFVLGH
EFSVIATPGHTLGHICYFSKPYLFCGDTLFSGGCGRLFEGTASQMYQSLK
KLSALPDDTLVCCAHEYTLSNMKFALSILPHDLSINDYYRKVKELRAKNQ
ITLPVILKNERQINVFLRTEDIDLINVINEETLLQQPEERFAWLRSKKDR
F
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
6rz0 Chain A Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
6rz0
Crystal structure of Escherichia coli Glyoxalase II
Resolution
1.1 Å
Binding residue
(original residue number in PDB)
D57 H58 D127 H165
Binding residue
(residue number reindexed from 1)
D57 H58 D127 H165
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H53 H55 D57 H58 H110 D127 H165
Catalytic site (residue number reindexed from 1)
H53 H55 D57 H58 H110 D127 H165
Enzyme Commision number
3.1.2.6
: hydroxyacylglutathione hydrolase.
Gene Ontology
Molecular Function
GO:0004416
hydroxyacylglutathione hydrolase activity
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0009408
response to heat
GO:0009636
response to toxic substance
GO:0019243
methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione
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Molecular Function
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Biological Process
External links
PDB
RCSB:6rz0
,
PDBe:6rz0
,
PDBj:6rz0
PDBsum
6rz0
PubMed
UniProt
P0AC84
|GLO2_ECOLI Hydroxyacylglutathione hydrolase GloB (Gene Name=gloB)
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