Structure of PDB 1m99 Chain A Binding Site BS01
Receptor Information
>1m99 Chain A (length=216) Species:
6182
(Schistosoma japonicum) [
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MSPILGYWKIKGLVQPTRLLLEYLEEKYEEHLYERDEGDKWRNKKFELGL
EFPNLPYYIDGDVKLTQSMAIIRYIADKHNMLGGCPKERAEISMLEGAVL
DIRYGVSRIAYSKDFETLKVDFLSKLPEMLKMFEDRLCHKTYLNGDHVTH
PDFMLYDALDVVLYMDPMCLDAFPKLVCFKKRIEAIPQIDKYLKSSKYIA
WPLQGWQATFGGGDHP
Ligand information
Ligand ID
GTS
InChI
InChI=1S/C10H17N3O9S/c11-5(10(18)19)1-2-7(14)13-6(4-23(20,21)22)9(17)12-3-8(15)16/h5-6H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)(H,20,21,22)/t5-,6-/m0/s1
InChIKey
QGWRMTHFAZVWAM-WDSKDSINSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(CC(=O)NC(CS(=O)(=O)O)C(=O)NCC(=O)O)C(C(=O)O)N
CACTVS 3.341
N[CH](CCC(=O)N[CH](C[S](O)(=O)=O)C(=O)NCC(O)=O)C(O)=O
OpenEye OEToolkits 1.5.0
C(CC(=O)N[C@@H](CS(=O)(=O)O)C(=O)NCC(=O)O)[C@@H](C(=O)O)N
CACTVS 3.341
N[C@@H](CCC(=O)N[C@@H](C[S](O)(=O)=O)C(=O)NCC(O)=O)C(O)=O
ACDLabs 10.04
O=C(NC(C(=O)NCC(=O)O)CS(=O)(=O)O)CCC(C(=O)O)N
Formula
C10 H17 N3 O9 S
Name
GLUTATHIONE SULFONIC ACID
ChEMBL
DrugBank
DB03003
ZINC
ZINC000001616624
PDB chain
1m99 Chain A Residue 220 [
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Receptor-Ligand Complex Structure
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PDB
1m99
Characterization of the electrophile binding site and substrate binding mode of the 26-kDa glutathione S-transferase from Schistosoma japonicum
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
Y7 W8 L13 W41 K45 N54 L55 Q67 S68
Binding residue
(residue number reindexed from 1)
Y7 W8 L13 W41 K45 N54 L55 Q67 S68
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
Y7 L13
Catalytic site (residue number reindexed from 1)
Y7 L13
Enzyme Commision number
2.5.1.18
: glutathione transferase.
Gene Ontology
Molecular Function
GO:0004364
glutathione transferase activity
GO:0016740
transferase activity
Biological Process
GO:0006749
glutathione metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1m99
,
PDBe:1m99
,
PDBj:1m99
PDBsum
1m99
PubMed
12596270
UniProt
P08515
|GST26_SCHJA Glutathione S-transferase class-mu 26 kDa isozyme
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