Structure of PDB 5fnb Chain A Binding Site BS02
Receptor Information
>5fnb Chain A (length=329) Species:
5323
(Pleurotus eryngii) [
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ATCDDGRTTANAACCILFPILDDIQENLFDGAQCGEKVRESLRLTFHDAI
GFSPTLGGGGADGSIIAFDTIETNFPANAGIDEIVSAQKPFVAKHNISAG
DFIQFAGAVGVSNCPGGVRIPFFLGRPDAVAASPDHLVPEPFDSVDSILA
RMGDAGFSPAEVVWLLASHSIAAADKVDPSIPGMPFDSTPGVFDSQFFIE
TLLKGRLFPGTAANKGEAQSPLQGEIRLQSDHLLARDPQTACEWQSMVNN
QPKIQNRFAATMSKMALLGQDKTKLIDCSDVIPTPPALVGAAHLPAGFSL
SDVEQACAATPFPALTADPGPVTSVPPVP
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
5fnb Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5fnb
Unveiling the Basis of Alkaline Stability of an Evolved Versatile Peroxidase.
Resolution
1.792 Å
Binding residue
(original residue number in PDB)
S170 D187 T189 V192 D194
Binding residue
(residue number reindexed from 1)
S170 D187 T189 V192 D194
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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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5fnb
,
PDBe:5fnb
,
PDBj:5fnb
PDBsum
5fnb
PubMed
27118867
UniProt
O94753
|VPL2_PLEER Versatile peroxidase VPL2 (Gene Name=vpl2)
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