Structure of PDB 2htn Chain A Binding Site BS02
Receptor Information
>2htn Chain A (length=158) Species:
511693
(Escherichia coli BL21) [
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MKGDTKVINYLNKLLGNELVAINQYFLHARMFKNWGLKRLNDVEYHESID
EMKHADRYIERILFLEGLPNLQDLGKLNIGEDVEEMLRSDLALELDGAKN
LREAIGYADSVHDYVSRDMMIEILRDEEGHIDWLETELDLIQKMGLQNYL
QAQIREEG
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
2htn Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
2htn
Fortuitous structure determination of 'as-isolated' Escherichia coli bacterioferritin in a novel crystal form.
Resolution
2.5 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:2htn
,
PDBe:2htn
,
PDBj:2htn
PDBsum
2htn
PubMed
17077480
UniProt
P0ABD3
|BFR_ECOLI Bacterioferritin (Gene Name=bfr)
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