Structure of PDB 1qpa Chain B Binding Site BS07
Receptor Information
>1qpa Chain B (length=344) [
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VACPDGVHTASNAACCAWFPVLDDIQQNLFHGGQCGAEAHEALRMVFHDS
IAISPKLQSQGKFGGGGADGSIITFSSIETTYHPNIGLDEVVAIQKPFIA
KHGVTPGDFIAFAGAVGVSNCPGAPQMQFFLGRPEATQAAPDGLVPEPFH
TIDQVLARMLDAGGFDEIETVWLLSAHSIAAANDVDPTISGLPFDSTPGQ
FDSQFFVETQLRGTAFPGKTGIQGTVMSPLKGEMRLQTDHLFARDSRTAC
EWQSFVNNQTKLQEDFQFIFTALSTLGHDMNAMIDCSEVIPAPKPVNFGP
SFFPAGKTHADIEQACASTPFPTLITAPGPSASVARIPPPPSPN
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
1qpa Chain B Residue 352 [
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Receptor-Ligand Complex Structure
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PDB
1qpa
The crystal structure of lignin peroxidase at 1.70 A resolution reveals a hydroxy group on the cbeta of tryptophan 171: a novel radical site formed during the redox cycle.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D48 G66 D68 S70
Binding residue
(residue number reindexed from 1)
D49 G67 D69 S71
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:1qpa
,
PDBe:1qpa
,
PDBj:1qpa
PDBsum
1qpa
PubMed
10024453
UniProt
P11542
|LIG4_PHACH Ligninase H2 (Gene Name=GLG4)
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