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8AWW

Transthyretin conjugated with a tafamidis derivative

8AWW の概要
エントリーDOI10.2210/pdb8aww/pdb
関連するPDBエントリー3tct
分子名称Transthyretin, ~{N}-(6-azanylhexyl)-2-[3,5-bis(chloranyl)phenyl]-1,3-benzoxazole-6-carboxamide (3 entities in total)
機能のキーワードttr, tafamidis, protein-drug conjugates, drug design, cancer therapy., transport protein
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数2
化学式量合計26219.05
構造登録者
主引用文献Cerofolini, L.,Vasa, K.,Bianconi, E.,Salobehaj, M.,Cappelli, G.,Bonciani, A.,Licciardi, G.,Perez-Rafols, A.,Padilla-Cortes, L.,Antonacci, S.,Rizzo, D.,Ravera, E.,Viglianisi, C.,Calderone, V.,Parigi, G.,Luchinat, C.,Macchiarulo, A.,Menichetti, S.,Fragai, M.
Combining Solid-State NMR with Structural and Biophysical Techniques to Design Challenging Protein-Drug Conjugates.
Angew.Chem.Int.Ed.Engl., 62:e202303202-e202303202, 2023
Cited by
PubMed Abstract: Several protein-drug conjugates are currently being used in cancer therapy. These conjugates rely on cytotoxic organic compounds that are covalently attached to the carrier proteins or that interact with them via non-covalent interactions. Human transthyretin (TTR), a physiological protein, has already been identified as a possible carrier protein for the delivery of cytotoxic drugs. Here we show the structure-guided development of a new stable cytotoxic molecule based on a known strong binder of TTR and a well-established anticancer drug. This example is used to demonstrate the importance of the integration of multiple biophysical and structural techniques, encompassing microscale thermophoresis, X-ray crystallography and NMR. In particular, we show that solid-state NMR has the ability to reveal effects caused by ligand binding which are more easily relatable to structural and dynamical alterations that impact the stability of macromolecular complexes.
PubMed: 37276329
DOI: 10.1002/anie.202303202
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.6 Å)
構造検証レポート
Validation report summary of 8aww
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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