Structure of PDB 1aeh Chain A Binding Site BS02
Receptor Information
>1aeh Chain A (length=291) Species:
4932
(Saccharomyces cerevisiae) [
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LVHVASVEKGRSYEDFQKVYNAIALKLREDDEYDNYIGYGPVLVRLAWHI
SGTWDKHDNTGGSYGGTYRFKKEFNDPSNAGLQNGFKFLEPIHKEFPWIS
SGDLFSLGGVTAVQEMQGPKIPWRCGRVDTPEDTTPDNGRLPDADKDAGY
VRTFFQRLNMNDREVVALMGAHALGKTHLKNSGYEGPGGAANNVFTNEFY
LNLLNEDWKLEKNDANNEQWDSKSGYMMLPTDYSLIQDPKYLSIVKEYAN
DQDKFFKDFSKAFEKLLEDGITFPKDAPSPFIFKTLEEQGL
Ligand information
Ligand ID
24T
InChI
InChI=1S/C4H6N2S/c1-3-2-7-4(5)6-3/h2H,1H3,(H2,5,6)
InChIKey
OUQMXTJYCAJLGO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1csc(N)n1
ACDLabs 10.04
n1c(csc1N)C
OpenEye OEToolkits 1.5.0
Cc1csc(n1)N
Formula
C4 H6 N2 S
Name
2-AMINO-4-METHYLTHIAZOLE
ChEMBL
CHEMBL505019
DrugBank
ZINC
ZINC000005438431
PDB chain
1aeh Chain A Residue 296 [
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Receptor-Ligand Complex Structure
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PDB
1aeh
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 T180 L232 D235
Binding residue
(residue number reindexed from 1)
H172 K176 T177 L229 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:1aeh
,
PDBe:1aeh
,
PDBj:1aeh
PDBsum
1aeh
PubMed
11812152
UniProt
P00431
|CCPR_YEAST Cytochrome c peroxidase, mitochondrial (Gene Name=CCP1)
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