Structure of PDB 4fi7 Chain A Binding Site BS01
Receptor Information
>4fi7 Chain A (length=116) Species:
9606
(Homo sapiens) [
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CPLMVKVLDAVRGSPAINVAVHVFRKAADDTWEPFASGKTSESGELHGLT
TEEEFVEGIYKVEIDTKSYWKALGISPFHEHAEVVFTANDSGPRRYTIAA
LLSPYSYSTTAVVTNP
Ligand information
Ligand ID
0UA
InChI
InChI=1S/C14H7Cl2FN2O4S/c15-10-5-8(6-11(16)12(10)20)14-19-18-13(23-14)7-2-1-3-9(4-7)24(17,21)22/h1-6,20H
InChIKey
QNTFSMWZVMUNMD-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
Oc1c(Cl)cc(cc1Cl)c2oc(nn2)c3cccc(c3)[S](F)(=O)=O
ACDLabs 12.01
FS(=O)(=O)c3cccc(c1nnc(o1)c2cc(Cl)c(O)c(Cl)c2)c3
OpenEye OEToolkits 1.7.6
c1cc(cc(c1)S(=O)(=O)F)c2nnc(o2)c3cc(c(c(c3)Cl)O)Cl
Formula
C14 H7 Cl2 F N2 O4 S
Name
3-[5-(3,5-dichloro-4-hydroxyphenyl)-1,3,4-oxadiazol-2-yl]benzenesulfonyl fluoride
ChEMBL
DrugBank
ZINC
ZINC000098207872
PDB chain
4fi7 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4fi7
Aromatic Sulfonyl Fluorides Covalently Kinetically Stabilize Transthyretin to Prevent Amyloidogenesis while Affording a Fluorescent Conjugate.
Resolution
1.402 Å
Binding residue
(original residue number in PDB)
K15 E54 T106 L110 S117 T118
Binding residue
(residue number reindexed from 1)
K6 E45 T97 L101 S108 T109
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:4fi7
,
PDBe:4fi7
,
PDBj:4fi7
PDBsum
4fi7
PubMed
23350654
UniProt
P02766
|TTHY_HUMAN Transthyretin (Gene Name=TTR)
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