6FKL
Tubulin-TUB015 complex
6FKL の概要
エントリーDOI | 10.2210/pdb6fkl/pdb |
分子名称 | Tubulin alpha-1B chain, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, 2-{1-[(2-Methoxyphenyl)amino]ethylidene}-5-phenyl-1,3-cyclohexanedione, ... (13 entities in total) |
機能のキーワード | cell cycle, tubulin fold, cytoskeleton, microtubule |
由来する生物種 | Rattus norvegicus (Rat) 詳細 |
細胞内の位置 | Cytoplasm, cytoskeleton: P81947 Q6B856 Golgi apparatus : P63043 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 265441.42 |
構造登録者 | |
主引用文献 | Bueno, O.,Estevez Gallego, J.,Martins, S.,Prota, A.E.,Gago, F.,Gomez-SanJuan, A.,Camarasa, M.J.,Barasoain, I.,Steinmetz, M.O.,Diaz, J.F.,Perez-Perez, M.J.,Liekens, S.,Priego, E.M. High-affinity ligands of the colchicine domain in tubulin based on a structure-guided design. Sci Rep, 8:4242-4242, 2018 Cited by PubMed Abstract: Microtubule-targeting agents that bind at the colchicine-site of tubulin are of particular interest in antitumoral therapy due to their dual mechanism of action as antimitotics and vascular disrupting agents. Cyclohexanediones derivatives have been described as a new family of colchicine-domain binders with an association constant to tubulin similar to that of colchicine. Here, the high-resolution structures of tubulin in complex with cyclohexanediones TUB015 and TUB075 were solved by X-ray crystallography. A detailed analysis of the tubulin-TUB075 interaction by means of computational affinity maps allowed the identification of two additional regions at the binding site that were addressed with the design and synthesis of a new series of cyclohexanediones with a distal 2-substituted benzofurane. These new compounds showed potent antiproliferative activity with IC values in the nM range, arrested cell cycle progression at the G/M phase and induced apoptosis at sub μM concentrations. Moreover, they caused the destruction of a preformed vascular network in vitro and inhibited the migration of endothelial cells at non-toxic concentrations. Finally, these compounds displayed high affinity for tubulin as substantiated by a K value of 2.87 × 10 M which, to the best of our knowledge, represents the highest binding constant measured to date for a colchicine-domain ligand. PubMed: 29523799DOI: 10.1038/s41598-018-22382-x 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.098 Å) |
構造検証レポート
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