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5U4E

Wild-type Transthyretin in complex with 3-[(1E)-2-(2-Chloro-4-boronic acid)ethenyl]benzoic Acid

Summary for 5U4E
Entry DOI10.2210/pdb5u4e/pdb
Related5U48 5U49 5U4A 5U4B 5U4C 5U4D 5U4F 5U4G
DescriptorTransthyretin, 3-[(E)-2-(4-borono-2-chlorophenyl)ethenyl]benzoic acid (3 entities in total)
Functional Keywordsboronic acids, medicinal chemistry, stilbene, covalent ligand, transport protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight28422.15
Authors
Windsor, I.W.,Smith, T.P.,Raines, R.T.,Forest, K.T. (deposition date: 2016-12-03, release date: 2017-09-27, Last modification date: 2023-10-04)
Primary citationSmith, T.P.,Windsor, I.W.,Forest, K.T.,Raines, R.T.
Stilbene Boronic Acids Form a Covalent Bond with Human Transthyretin and Inhibit Its Aggregation.
J. Med. Chem., 60:7820-7834, 2017
Cited by
PubMed: 28920684
DOI: 10.1021/acs.jmedchem.7b00952
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.45 Å)
Structure validation

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