Structure of PDB 1nfv Chain D Binding Site BS03
Receptor Information
>1nfv Chain D (length=170) Species:
876
(Desulfovibrio desulfuricans) [
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GNREDRKAKVIEVLNKARAMELHAIHQYMNQHYSLDDMDYGELAANMKLI
AIDEMRHAENFAERIKELGGEPTTQKEGKVVTGQAVPVIYESDADQEDAT
IEAYSQFLKVCKEQGDIVTARLFERIIEEEQAHLTYYENIGSHIKNLGDT
YLAKIAGTPSSTGTASKGFV
Ligand information
Ligand ID
3PY
InChI
InChI=1S/C3H4O4/c4-1-2(5)3(6)7/h4H,1H2,(H,6,7)
InChIKey
HHDDCCUIIUWNGJ-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)C(=O)CO
CACTVS 3.341
OCC(=O)C(O)=O
OpenEye OEToolkits 1.5.0
C(C(=O)C(=O)O)O
Formula
C3 H4 O4
Name
3-HYDROXYPYRUVIC ACID
ChEMBL
CHEMBL1230192
DrugBank
DB02951
ZINC
ZINC000001532558
PDB chain
1nfv Chain D Residue 1310 [
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Receptor-Ligand Complex Structure
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PDB
1nfv
The nature of the di-iron site in the bacterioferritin from Desulfovibrio desulfuricans
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
R127 E131
Binding residue
(residue number reindexed from 1)
R125 E129
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.16.3.1
: ferroxidase.
Gene Ontology
Molecular Function
GO:0003674
molecular_function
GO:0004322
ferroxidase activity
GO:0005506
iron ion binding
GO:0008199
ferric iron binding
GO:0015093
ferrous iron transmembrane transporter activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006826
iron ion transport
GO:0006879
intracellular iron ion homeostasis
GO:0006880
intracellular sequestering of iron ion
GO:0034755
iron ion transmembrane transport
Cellular Component
GO:0005575
cellular_component
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:1nfv
,
PDBe:1nfv
,
PDBj:1nfv
PDBsum
1nfv
PubMed
12627224
UniProt
Q93PP9
|BFR_DESDA Bacterioferritin (Gene Name=bfr)
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