Structure of PDB 4tqi Chain B Binding Site BS01
Receptor Information
>4tqi Chain B (length=116) Species:
9606
(Homo sapiens) [
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CPLMVKVLDAVRGSPAINVAVHVFRKAADDTWEPFASGKTSESGELHGLT
TEEEFVEGIYKVEIDTKSYWKALGISPFHEHAEVVFTANDSGPRRYTIAA
LLSPYSYSTTAVVTNP
Ligand information
Ligand ID
6BD
InChI
InChI=1S/C17H15NO3/c1-11(17(19)20)10-21-18-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11H,10H2,1H3,(H,19,20)/t11-/m0/s1
InChIKey
ZHFDVDMCVXUGGF-NSHDSACASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(CON=C1c2ccccc2-c3c1cccc3)C(=O)O
ACDLabs 10.04
O=C(O)C(C)CO\N=C3/c1ccccc1c2c3cccc2
OpenEye OEToolkits 1.5.0
C[C@@H](CON=C1c2ccccc2-c3c1cccc3)C(=O)O
CACTVS 3.341
C[CH](CON=C1c2ccccc2c3ccccc13)C(O)=O
CACTVS 3.341
C[C@@H](CON=C1c2ccccc2c3ccccc13)C(O)=O
Formula
C17 H15 N O3
Name
(2S)-3-[(9H-fluoren-9-ylideneamino)oxy]-2-methylpropanoic acid;
(S)-3-(9H-fluoren-9-ylideneaminooxy)-2-methylpropanoic acid
ChEMBL
DrugBank
DB07201
ZINC
ZINC000053682981
PDB chain
4tqi Chain B Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
4tqi
X-ray crystal structure and activity of fluorenyl-based compounds as transthyretin fibrillogenesis inhibitors.
Resolution
1.25 Å
Binding residue
(original residue number in PDB)
K15 L17
Binding residue
(residue number reindexed from 1)
K6 L8
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005179
hormone activity
GO:0005515
protein binding
GO:0042802
identical protein binding
GO:0070324
thyroid hormone binding
Biological Process
GO:0006144
purine nucleobase metabolic process
GO:0007165
signal transduction
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0005737
cytoplasm
GO:0035578
azurophil granule lumen
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4tqi
,
PDBe:4tqi
,
PDBj:4tqi
PDBsum
4tqi
PubMed
26235916
UniProt
P02766
|TTHY_HUMAN Transthyretin (Gene Name=TTR)
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