Structure of PDB 2z8k Chain B Binding Site BS01
Receptor Information
>2z8k Chain B (length=190) Species:
562
(Escherichia coli) [
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TTHYSVVDKDGNAVAVTYTLNTTFGTGIVAGESGILLNNQMDDFSAKPGV
PNVYGLVGGDANAVGPNKRPLSSMSPTIVVKDGKTWLVTGSPGGSRIITT
VLQMVVNSIDYGLNVAEATNAPRFHHQWLPDELRVEKGFSPDTLKLLEAK
GQKVALKEAMGSTQSIMVGPDGELYGASDPRSVDDLTAGY
Ligand information
Ligand ID
AVN
InChI
InChI=1S/C5H7ClN2O3/c6-3-1-2(11-8-3)4(7)5(9)10/h2,4H,1,7H2,(H,9,10)/t2-,4-/m0/s1
InChIKey
QAWIHIJWNYOLBE-OKKQSCSOSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1C(ON=C1Cl)C(C(=O)O)N
CACTVS 3.341
N[C@@H]([C@@H]1CC(=NO1)Cl)C(O)=O
OpenEye OEToolkits 1.5.0
C1[C@H](ON=C1Cl)[C@@H](C(=O)O)N
CACTVS 3.341
N[CH]([CH]1CC(=NO1)Cl)C(O)=O
ACDLabs 10.04
ClC1=NOC(C(C(=O)O)N)C1
Formula
C5 H7 Cl N2 O3
Name
(2S)-AMINO[(5S)-3-CHLORO-4,5-DIHYDROISOXAZOL-5-YL]ACETIC ACID;
ACIVICIN
ChEMBL
CHEMBL1231101
DrugBank
ZINC
ZINC000003871381
PDB chain
2z8k Chain B Residue 390 [
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Receptor-Ligand Complex Structure
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PDB
2z8k
Crystal structures of Escherichia coli gamma-glutamyltranspeptidase in complex with azaserine and acivicin: novel mechanistic implication for inhibition by glutamine antagonists
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
T391 T409 N411 D433 Y444 S462 S463 M464 G484
Binding residue
(residue number reindexed from 1)
T1 T19 N21 D43 Y54 S72 S73 M74 G94
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.3.2.2
: gamma-glutamyltransferase.
3.4.19.13
: glutathione gamma-glutamate hydrolase.
Gene Ontology
Molecular Function
GO:0036374
glutathione hydrolase activity
Biological Process
GO:0006751
glutathione catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2z8k
,
PDBe:2z8k
,
PDBj:2z8k
PDBsum
2z8k
PubMed
18555071
UniProt
P18956
|GGT_ECOLI Glutathione hydrolase proenzyme (Gene Name=ggt)
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