Structure of PDB 7c89 Chain D Binding Site BS02
Receptor Information
>7c89 Chain D (length=244) Species:
272557
(Aeropyrum pernix K1) [
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PGSIPLIGERFPEMEVTTDHGVIKLPDHYVSQGKWFVLFSHPADFTPVST
TEFVSFARRYEDFQRLGVDLIGLSVDSVCSHIKWKEWIERHIGVRIPFPI
IADPQGTVARRLGLLHAESATHTVRGVFIVDARGVIRTMLYYPMELGRLV
DEILRIVKALKLGDSLKRAVPADWPNNEIIGEGLIVPPPTTEDQARARME
SGQYRSLDWWFSWDTPASRDDVEEARRYLRRAAEKPAKLLYEEA
Ligand information
Ligand ID
FL0
InChI
InChI=1S/C8H7BrO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2
InChIKey
LIGACIXOYTUXAW-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
c1ccc(cc1)C(=O)CBr
CACTVS 3.385
BrCC(=O)c1ccccc1
Formula
C8 H7 Br O
Name
2-bromanyl-1-phenyl-ethanone
ChEMBL
CHEMBL102953
DrugBank
ZINC
ZINC000000331704
PDB chain
7c89 Chain D Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
7c89
Rebuilding Ring-Type Assembly of Peroxiredoxin by Chemical Modification.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
V79 C80
Binding residue
(residue number reindexed from 1)
V78 C79
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.11.1.24
: thioredoxin-dependent peroxiredoxin.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0008379
thioredoxin peroxidase activity
GO:0016209
antioxidant activity
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0051920
peroxiredoxin activity
GO:0140824
thioredoxin-dependent peroxiredoxin activity
Biological Process
GO:0006979
response to oxidative stress
GO:0033554
cellular response to stress
GO:0042744
hydrogen peroxide catabolic process
GO:0045454
cell redox homeostasis
GO:0070301
cellular response to hydrogen peroxide
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7c89
,
PDBe:7c89
,
PDBj:7c89
PDBsum
7c89
PubMed
33334100
UniProt
Q9Y9L0
|TDXH_AERPE Peroxiredoxin (Gene Name=APE_2278)
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