Structure of PDB 1qgj Chain A Binding Site BS02
Receptor Information
>1qgj Chain A (length=300) Species:
3702
(Arabidopsis thaliana) [
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QLSPDIYAKSCPNLVQIVRKQVAIALKAEIRMAASLIRLHFHDCFVNGCD
ASLLLDGADSEKLAIPNINSARGFEVIDTIKAAVENACPGVVSCADILTL
AARDSVVLSGGPGWRVALGRKDGLVANQNSANNLPSPFEPLDAIIAKFVA
VNLNITDVVALSGAHTFGQAKCAVFSNRLFNFTGAGNPDATLETSLLSNL
QTVCPLGGNSNITAPLDRSTTDTFDNNYFKNLLEGKGLLSSDQILFSSDL
AVNTTKKLVEAYSRSQSLFFRDFTCAMIRMGNISNGASGEVRTNCRVINN
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1qgj Chain A Residue 2002 [
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Receptor-Ligand Complex Structure
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PDB
1qgj
Arabidopsis thaliana peroxidase N: structure of a novel neutral peroxidase.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
T166 D217 T220 T223 D225
Binding residue
(residue number reindexed from 1)
T166 D217 T220 T223 D225
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R38 H42 N67 H165
Catalytic site (residue number reindexed from 1)
R38 H42 N67 H165
Enzyme Commision number
1.11.1.7
: peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0140825
lactoperoxidase activity
Biological Process
GO:0006979
response to oxidative stress
GO:0042744
hydrogen peroxide catabolic process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005576
extracellular region
GO:0005634
nucleus
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1qgj
,
PDBe:1qgj
,
PDBj:1qgj
PDBsum
1qgj
PubMed
10713531
UniProt
Q39034
|PER59_ARATH Peroxidase 59 (Gene Name=PER59)
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