Structure of PDB 3fm1 Chain A Binding Site BS05
Receptor Information
>3fm1 Chain A (length=319) Species:
5323
(Pleurotus eryngii) [
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ATCDDGRTTANAACCILFPILDDIQENLFDGAQCGEEVHESLRLTFHDAI
GFSPTLGGGGADGSIIAFDTIETNFPANAGIDEIVSAQKPFVAKHNISAG
DFIQFAGAVGVSNCPGGVRIPFFLGRPDAVAASPDHLVPEPFDSVDSILA
RMGDAGFSPVEVVWLLASHSIAAADKVDPSIPGTPFDSTPQVFDSQFFIE
TQLKGRLFPGTADNKGEAQSPLQGEIRLQSDHLLARDPQTACEWQSMVNN
QPKIQNRFAATMSKMALLGQDKTKLIDCSDVIPTPPALVGAAHLPAGFSL
SDVEQACAATPFPALTADP
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
3fm1 Chain A Residue 334 [
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Receptor-Ligand Complex Structure
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PDB
3fm1
Structural and Site-directed Mutagenesis Study of Versatile Peroxidase Oxidizing both Mn(II) and Aromatic Substrates
Resolution
1.78 Å
Binding residue
(original residue number in PDB)
H293 D318
Binding residue
(residue number reindexed from 1)
H293 D318
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R43 H47 H169 F186 D231
Catalytic site (residue number reindexed from 1)
R43 H47 H169 F186 D231
Enzyme Commision number
1.11.1.16
: versatile peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0016689
manganese peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0052750
reactive-black-5:hydrogen-peroxide oxidoreductase activity
Biological Process
GO:0000302
response to reactive oxygen species
GO:0006979
response to oxidative stress
GO:0034599
cellular response to oxidative stress
GO:0042744
hydrogen peroxide catabolic process
GO:0046274
lignin catabolic process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005576
extracellular region
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Cellular Component
External links
PDB
RCSB:3fm1
,
PDBe:3fm1
,
PDBj:3fm1
PDBsum
3fm1
PubMed
UniProt
O94753
|VPL2_PLEER Versatile peroxidase VPL2 (Gene Name=vpl2)
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