Structure of PDB 5ihh Chain A Binding Site BS01
Receptor Information
>5ihh Chain A (length=116) Species:
9606
(Homo sapiens) [
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CPLMVKVLDAVRGSPAINVAVHVFRKAADDTWEPFASGKTSESGELHGLT
TEEEFVEGIYKVEIDTKSYWKALGISPFHEHAEVVFTANDSGPRRYTIAA
LLSPYSYSTTAVVTNP
Ligand information
Ligand ID
6B5
InChI
InChI=1S/C16H12O6/c1-21-9-5-12(19)16-13(20)7-14(22-15(16)6-9)8-2-3-10(17)11(18)4-8/h2-7,17-19H,1H3
InChIKey
RRRSSAVLTCVNIQ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.4
COc1cc(c2c(c1)OC(=CC2=O)c3ccc(c(c3)O)O)O
ACDLabs 12.01
c3cc(C=1Oc2c(C(=O)C=1)c(cc(c2)OC)O)cc(c3O)O
CACTVS 3.385
COc1cc(O)c2C(=O)C=C(Oc2c1)c3ccc(O)c(O)c3
Formula
C16 H12 O6
Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4H-1-chromen-4-one;
7,8-DIMETHYLALLOXAZINE;
6,7-DIMETHYLALLOXAZINE
ChEMBL
CHEMBL183745
DrugBank
ZINC
ZINC000014813714
PDB chain
5ihh Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
5ihh
Modifications of the 7-Hydroxyl Group of the Transthyretin Ligand Luteolin Provide Mechanistic Insights into Its Binding Properties and High Plasma Specificity.
Resolution
1.35 Å
Binding residue
(original residue number in PDB)
K15 L17 L110 S117 T119
Binding residue
(residue number reindexed from 1)
K6 L8 L101 S108 T110
Annotation score
1
Binding affinity
MOAD
: Kd=390nM
PDBbind-CN
: -logKd/Ki=6.41,Kd=390nM
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:5ihh
,
PDBe:5ihh
,
PDBj:5ihh
PDBsum
5ihh
PubMed
27050398
UniProt
P02766
|TTHY_HUMAN Transthyretin (Gene Name=TTR)
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