Structure of PDB 3e1n Chain E Binding Site BS02
Receptor Information
>3e1n Chain E (length=156) Species:
83333
(Escherichia coli K-12) [
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MKGDTKVINYLNKLLGNELVAINQYFLHARMFKNWGLKRLNDVEYHESID
EMKHADRYIERILFLEGLPNLQDLGKLNIGEDVEEMLRSDLALELDGAKN
LREAIGYADSVHDYVSRDMMIEILRDEEGHIDWLETELDLIQKMGLQNYL
QAQIRE
Ligand information
Ligand ID
FE2
InChI
InChI=1S/Fe/q+2
InChIKey
CWYNVVGOOAEACU-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Fe+2]
CACTVS 3.341
[Fe++]
Formula
Fe
Name
FE (II) ION
ChEMBL
DrugBank
DB14510
ZINC
PDB chain
3e1n Chain E Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
3e1n
Structural basis for iron mineralization by bacterioferritin
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
E51 E94 E127 H130
Binding residue
(residue number reindexed from 1)
E51 E94 E127 H130
Annotation score
5
Enzymatic activity
Enzyme Commision number
1.16.3.1
: ferroxidase.
Gene Ontology
Molecular Function
GO:0004322
ferroxidase activity
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0008199
ferric iron binding
GO:0015093
ferrous iron transmembrane transporter activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0140315
iron ion sequestering activity
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:0005829
cytosol
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3e1n
,
PDBe:3e1n
,
PDBj:3e1n
PDBsum
3e1n
PubMed
19391621
UniProt
P0ABD3
|BFR_ECOLI Bacterioferritin (Gene Name=bfr)
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