Structure of PDB 1bfr Chain S Binding Site BS02
Receptor Information
>1bfr Chain S (length=158) Species:
562
(Escherichia coli) [
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MKGDTKVINYLNKLLGNELVAINQYFLHARMFKNWGLKRLNDVEYHESID
EMKHADRYIERILFLEGLPNLQDLGKLNIGEDVEEMLRSDLALELDGAKN
LREAIGYADSVHDYVSRDMMIEILRDEEGHIDWLETELDLIQKMGLQNYL
QAQIREEG
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
1bfr Chain S Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
1bfr
Structure of a monoclinic crystal from of cyctochrome b1 (Bacterioferritin) from E. coli.
Resolution
2.94 Å
Binding residue
(original residue number in PDB)
E18 E51 H54 E127
Binding residue
(residue number reindexed from 1)
E18 E51 H54 E127
Annotation score
1
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:1bfr
,
PDBe:1bfr
,
PDBj:1bfr
PDBsum
1bfr
PubMed
9867433
UniProt
P0ABD3
|BFR_ECOLI Bacterioferritin (Gene Name=bfr)
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