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8II2

Crystal structure of V30M-TTR in complex with BBM

Summary for 8II2
Entry DOI10.2210/pdb8ii2/pdb
DescriptorTransthyretin, [3,5-bis(bromanyl)-4-oxidanyl-phenyl]-(2-ethyl-1-benzofuran-3-yl)methanone, CALCIUM ION, ... (4 entities in total)
Functional Keywordsthyroxine, amyloidosis, inhibitor, transport protein
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight35573.41
Authors
Yokoyama, T. (deposition date: 2023-02-24, release date: 2023-06-28, Last modification date: 2024-05-29)
Primary citationMizuguchi, M.,Yokoyama, T.,Okada, T.,Nakagawa, Y.,Fujii, K.,Nabeshima, Y.,Toyooka, N.
Benziodarone and 6-hydroxybenziodarone are potent and selective inhibitors of transthyretin amyloidogenesis.
Bioorg.Med.Chem., 90:117370-117370, 2023
Cited by
PubMed Abstract: Transthyretin amyloidosis is a progressive systemic disorder that is caused by the amyloid deposition of transthyretin in various organs. Stabilization of the native transthyretin is an effective strategy for the treatment of transthyretin amyloidosis. In this study we demonstrate that the clinically used uricosuric agent benziodarone is highly effective to stabilize the tetrameric structure of transthyretin. An acid-induced aggregation assay showed that benziodarone had strong inhibitory activity similar to that of tafamidis, which is currently used as a therapeutic agent for transthyretin amyloidosis. Moreover, a possible metabolite, 6-hydroxybenziodarone, retained the strong amyloid inhibitory activity of benziodarone. An ex vivo competitive binding assay using a fluorogenic probe showed that benziodarone and 6-hydroxybenziodarone were highly potent for selective binding to transthyretin in human plasma. An X-ray crystal structure analysis revealed that the halogenated hydroxyphenyl ring was located at the entrance of the thyroxine binding channel of transthyretin and that the benzofuran ring was located in the inner channel. These studies suggest that benziodarone and 6-hydroxybenziodarone would potentially be effective against transthyretin amyloidosis.
PubMed: 37311373
DOI: 10.1016/j.bmc.2023.117370
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.798 Å)
Structure validation

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数据于2024-11-13公开中

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