Structure of PDB 1b82 Chain A Binding Site BS02
Receptor Information
>1b82 Chain A (length=349) [
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VIEKRATCSNGKTVGDASCCAWFDVLDDIQQNLFHGGQCGAEAHESIRLV
FHDSIAISPAMEAQGKFGGGGADGSIMIFDDIETAFHPNIGLDEIVKLQK
PFVQKHGVTPGDFIAFAGAVALSNCPGAPQMNFFTGRAPATQPAPDGLVP
EPFHTVDQIINRVNDAGEFDELELVWMLSAHSVAAVNDVDPTVQGLPFDS
TPGIFDSQFFVETQLRGTAFPGSGGNQGEVESPLPGEIRIQSDHTIARDS
RTACEWQSFVNNQSKLVDDFQFIFLALTQLGQDPNAMTDCSDVIPQSKPI
PGNLPFSFFPAGKTIKDVEQACAETPFPTLTTLPGPETSVQRIPPPPGA
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
1b82 Chain A Residue 1352 [
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Receptor-Ligand Complex Structure
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PDB
1b82
Crystal structures of pristine and oxidatively processed lignin peroxidase expressed in Escherichia coli and of the W171F variant that eliminates the redox active tryptophan 171. Implications for the reaction mechanism.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
S177 D194 T196 I199 D201
Binding residue
(residue number reindexed from 1)
S182 D199 T201 I204 D206
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H176 F193
Catalytic site (residue number reindexed from 1)
H181 F198
Enzyme Commision number
1.11.1.14
: lignin peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0016690
diarylpropane 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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1b82
,
PDBe:1b82
,
PDBj:1b82
PDBsum
1b82
PubMed
11162097
UniProt
P06181
|LIG8_PHACH Ligninase H8 (Gene Name=LPOA)
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