Structure of PDB 1b80 Chain B Binding Site BS02
Receptor Information
>1b80 Chain B (length=345) [
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RATCSNGKTVGDASCCAWFDVLDDIQQNLFHGGQCGAEAHESIRLVFHDS
IAISPAMEAQGKFGGGGADGSIMIFDDIETAFHPNIGLDEIVKLQKPFVQ
KHGVTPGDFIAFAGAVALSNCPGAPQMNFFTGRAPATQPAPDGLVPEPFH
TVDQIINRVNDAGEFDELELVWMLSAHSVAAVNDVDPTVQGLPFDSTPGI
FDSQFFVETQLRGTAFPGSGGNQGEVESPLPGEIRIQSDHTIARDSRTAC
EWQSFVNNQSKLVDDFQFIFLALTQLGQDPNAMTDCSDVIPQSKPIPGNL
PFSFFPAGKTIKDVEQACAETPFPTLTTLPGPETSVQRIPPPPGA
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
1b80 Chain B Residue 352 [
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Receptor-Ligand Complex Structure
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PDB
1b80
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
1.73 Å
Binding residue
(original residue number in PDB)
S177 D194 T196 I199 D201
Binding residue
(residue number reindexed from 1)
S178 D195 T197 I200 D202
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H176 F193
Catalytic site (residue number reindexed from 1)
H177 F194
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:1b80
,
PDBe:1b80
,
PDBj:1b80
PDBsum
1b80
PubMed
11162097
UniProt
P06181
|LIG8_PHACH Ligninase H8 (Gene Name=LPOA)
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