Structure of PDB 3fz5 Chain A Binding Site BS01
Receptor Information
>3fz5 Chain A (length=190) Species:
272943
(Cereibacter sphaeroides 2.4.1) [
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AMNPIEFWFDFSSGYAFFAAQRIEALAAELGRTVLWRPYMLGLSSTPLKR
DYAQRDWARIARQRGLTFRPPADHPHVALAATRAFYWIEAQSPDAATAFA
QRVFDLYFSDRLDTASPEAVSRLGPEVGLEPEALLAGIADPALKETVRKI
GEDAVARGIFGSPFFLVDDEPFWGWDRMEMMAEWIRTGGW
Ligand information
Ligand ID
GSH
InChI
InChI=1S/C10H17N3O6S/c11-5(10(18)19)1-2-7(14)13-6(4-20)9(17)12-3-8(15)16/h5-6,20H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)/t5-,6-/m0/s1
InChIKey
RWSXRVCMGQZWBV-WDSKDSINSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(NCC(=O)O)C(NC(=O)CCC(C(=O)O)N)CS
OpenEye OEToolkits 1.7.6
C(CC(=O)N[C@@H](CS)C(=O)NCC(=O)O)[C@@H](C(=O)O)N
CACTVS 3.370
N[CH](CCC(=O)N[CH](CS)C(=O)NCC(O)=O)C(O)=O
CACTVS 3.370
N[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O)C(O)=O
OpenEye OEToolkits 1.7.6
C(CC(=O)NC(CS)C(=O)NCC(=O)O)C(C(=O)O)N
Formula
C10 H17 N3 O6 S
Name
GLUTATHIONE
ChEMBL
CHEMBL1543
DrugBank
DB00143
ZINC
ZINC000003830891
PDB chain
3fz5 Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
3fz5
Crystal structure of possible 2-hydroxychromene-2-carboxylate isomerase from Rhodobacter sphaeroides
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
S12 Y14 G170 S171 W182 G183 W184 D185
Binding residue
(residue number reindexed from 1)
S13 Y15 G161 S162 W173 G174 W175 D176
Annotation score
1
Enzymatic activity
Enzyme Commision number
5.99.1.4
: 2-hydroxychromene-2-carboxylate isomerase.
Gene Ontology
Molecular Function
GO:0004364
glutathione transferase activity
GO:0004602
glutathione peroxidase activity
GO:0016491
oxidoreductase activity
GO:0016853
isomerase activity
GO:0018845
2-hydroxychromene-2-carboxylate isomerase activity
GO:0046872
metal ion binding
Biological Process
GO:0006749
glutathione metabolic process
GO:0098869
cellular oxidant detoxification
GO:1901170
naphthalene catabolic process
Cellular Component
GO:0005777
peroxisome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3fz5
,
PDBe:3fz5
,
PDBj:3fz5
PDBsum
3fz5
PubMed
UniProt
Q3J568
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