Structure of PDB 1yyd Chain A Binding Site BS04
Receptor Information
>1yyd Chain A (length=357) [
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AVCPDGTRVSHAACCAFIPLAQDLQETIFQNECGEDAHEVIRLTFHDAIA
ISRSQGPKAGGGADGSMLLFPTVEPNFSANNGIDDSVNNLIPFMQKHNTI
SAADLVQFAGAVALSNCPGAPRLEFLAGRPNKTIAAVDGLIPEPQDSVTK
ILQRFEDAGGFTPFEVVSLLASHSVARADKVDQTIDAAPFDSTPFTFDTQ
VFLEVLLKGVGFPGSANNTGEVASPLPLGSGSDTGEMRLQSDFALAHDPR
TACIWQGFVNEQAFMAASFRAAMSKLAVLGHNRNSLIDCSDVVPVPKPAT
GQPAMFPASTGPQDLELSCPSERFPTLTTQPGASQSLIAHCPDGSMSCPG
VQFNGPA
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
1yyd Chain A Residue 381 [
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Receptor-Ligand Complex Structure
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PDB
1yyd
High-Resolution Crystal Structure of Manganese Peroxidase: Substrate and Inhibitor Complexes.
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
E35 E39 D179
Binding residue
(residue number reindexed from 1)
E35 E39 D179
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
R42 H46 H173 F190 D242
Catalytic site (residue number reindexed from 1)
R42 H46 H173 F190 D242
Enzyme Commision number
1.11.1.13
: manganese peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0016689
manganese peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
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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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1yyd
,
PDBe:1yyd
,
PDBj:1yyd
PDBsum
1yyd
PubMed
15850380
UniProt
Q02567
|PEM1_PHACH Manganese peroxidase 1 (Gene Name=MNP1)
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