Structure of PDB 1aem Chain A Binding Site BS02
Receptor Information
>1aem Chain A (length=291) Species:
4932
(Saccharomyces cerevisiae) [
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LVHVASVEKGRSYEDFQKVYNAIALKLREDDEYDNYIGYGPVLVRLAWHI
SGTWDKHDNTGGSYGGTYRFKKEFNDPSNAGLQNGFKFLEPIHKEFPWIS
SGDLFSLGGVTAVQEMQGPKIPWRCGRVDTPEDTTPDNGRLPDADKDAGY
VRTFFQRLNMNDREVVALMGAHALGKTHLKNSGYEGPGGAANNVFTNEFY
LNLLNEDWKLEKNDANNEQWDSKSGYMMLPTDYSLIQDPKYLSIVKEYAN
DQDKFFKDFSKAFEKLLEDGITFPKDAPSPFIFKTLEEQGL
Ligand information
Ligand ID
MPI
InChI
InChI=1S/C7H6N2/c1-2-5-9-6-4-8-7(9)3-1/h1-6H/p+1
InChIKey
UTCSSFWDNNEEBH-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
[nH]1cc[n+]2ccccc12
ACDLabs 10.04
c1cccc2[n+]1ccn2
OpenEye OEToolkits 1.5.0
c1cc[n+]2cc[nH]c2c1
Formula
C7 H7 N2
Name
IMIDAZO[1,2-A]PYRIDINE
ChEMBL
DrugBank
ZINC
PDB chain
1aem Chain A Residue 296 [
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Receptor-Ligand Complex Structure
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PDB
1aem
Artificial protein cavities as specific ligand-binding templates: characterization of an engineered heterocyclic cation-binding site that preserves the evolved specificity of the parent protein.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
H175 K179 G191 M230 D235
Binding residue
(residue number reindexed from 1)
H172 K176 G188 M227 D232
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R48 H52 H175 G191 D235
Catalytic site (residue number reindexed from 1)
R45 H49 H172 G188 D232
Enzyme Commision number
1.11.1.5
: cytochrome-c peroxidase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0020037
heme binding
Biological Process
GO:0006979
response to oxidative stress
GO:0034599
cellular response to oxidative stress
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1aem
,
PDBe:1aem
,
PDBj:1aem
PDBsum
1aem
PubMed
11812152
UniProt
P00431
|CCPR_YEAST Cytochrome c peroxidase, mitochondrial (Gene Name=CCP1)
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