Structure of PDB 1e3b Chain A Binding Site BS01
Receptor Information
>1e3b Chain A (length=172) Species:
6239
(Caenorhabditis elegans) [
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MSRSKVFFDITIGGKASGRIVMELYDDVVPKTAGNFRALCTGENGIGKSG
KPLHFKGSKFHRIIPNFMIQGGDFTRGNGTGGESIYGEKFPDENFKEKHT
GPGVLSMANAGPNTNGSQFFLCTVKTEWLDGKHVVFGRVVEGLDVVKAVE
SNGSQSGKPVKDCMIADCGQLK
Ligand information
Ligand ID
3EP
InChI
InChI=1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
InChIKey
RXJKFRMDXUJTEX-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OpenEye OEToolkits 1.5.0
CCP(CC)CC
ACDLabs 10.04
P(CC)(CC)CC
Formula
C6 H15 P
Name
TRIETHYLPHOSPHANE
ChEMBL
DrugBank
ZINC
ZINC000001846538
PDB chain
1e3b Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
1e3b
First Crystal Structure of a Medicinally Relevant Gold Protein Complex:Unexpected Binding of [Au(Pet (3))](+) to Histidine
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
W128 K132
Binding residue
(residue number reindexed from 1)
W128 K132
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R62 F67 Q70 N109 F120 L129 H133
Catalytic site (residue number reindexed from 1)
R62 F67 Q70 N109 F120 L129 H133
Enzyme Commision number
5.2.1.8
: peptidylprolyl isomerase.
Gene Ontology
Molecular Function
GO:0003755
peptidyl-prolyl cis-trans isomerase activity
GO:0005515
protein binding
GO:0016018
cyclosporin A binding
Biological Process
GO:0000413
protein peptidyl-prolyl isomerization
GO:0006457
protein folding
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1e3b
,
PDBe:1e3b
,
PDBj:1e3b
PDBsum
1e3b
PubMed
11028014
UniProt
P52011
|CYP3_CAEEL Peptidyl-prolyl cis-trans isomerase 3 (Gene Name=cyn-3)
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