Structure of PDB 5agy Chain A Binding Site BS03
Receptor Information
>5agy Chain A (length=219) Species:
3847
(Glycine max) [
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MQDEVVLLDFWPSPFGMRVRIALAEKGIKYEYKEEDLQNKSPLLLKMNPV
HKKIPVLIHNGKPICESLIAVQYIEEVWNDRNPLLPSDPYQRAQTRFWAD
YVDKKIYDLGRKICTSKGEEKEAAKKEFIEALKLLEEQLGDKTYFGGDNL
GFVDIALVPFYTWFKAYETFGTLNIESECPKFVAWAKRCLQKESVAKSLP
DQQKVYEFIMDLRKKLGIE
Ligand information
Ligand ID
GTB
InChI
InChI=1S/C17H22N4O8S/c18-12(17(26)27)5-6-14(22)20-13(16(25)19-7-15(23)24)9-30-8-10-1-3-11(4-2-10)21(28)29/h1-4,12-13H,5-9,18H2,(H,19,25)(H,20,22)(H,23,24)(H,26,27)/t12-,13-/m0/s1
InChIKey
OAWORKDPTSAMBZ-STQMWFEESA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1cc(ccc1CSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)[N+](=O)[O-]
ACDLabs 12.01
O=[N+]([O-])c1ccc(cc1)CSCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N
OpenEye OEToolkits 1.7.0
c1cc(ccc1CSCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)[N+](=O)[O-]
CACTVS 3.370
N[CH](CCC(=O)N[CH](CSCc1ccc(cc1)[N+]([O-])=O)C(=O)NCC(O)=O)C(O)=O
CACTVS 3.370
N[C@@H](CCC(=O)N[C@@H](CSCc1ccc(cc1)[N+]([O-])=O)C(=O)NCC(O)=O)C(O)=O
Formula
C17 H22 N4 O8 S
Name
S-(P-NITROBENZYL)GLUTATHIONE
ChEMBL
DrugBank
DB03686
ZINC
ZINC000003874914
PDB chain
5agy Chain A Residue 1222 [
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Receptor-Ligand Complex Structure
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PDB
5agy
Directed Evolution of Tau Class Glutathione Transferases Reveals a Site that Regulates Catalytic Efficiency and Masks Cooperativity.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
F10 S13 F15 L37 K40 K53 I54 E66 S67 Y107 F208 L212
Binding residue
(residue number reindexed from 1)
F10 S13 F15 L37 K40 K53 I54 E66 S67 Y107 F208 L212
Annotation score
2
Enzymatic activity
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
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5agy
,
PDBe:5agy
,
PDBj:5agy
PDBsum
5agy
PubMed
26637269
UniProt
I1MJ34
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