5J3P
Crystal structure of the catalytic domain of human tyrosyl DNA phosphodiesterase 2
5J3P の概要
エントリーDOI | 10.2210/pdb5j3p/pdb |
分子名称 | Tyrosyl-DNA phosphodiesterase 2, MAGNESIUM ION, GLYCEROL, ... (4 entities in total) |
機能のキーワード | tyrosyl, dna phosphodiesterase 2, catalytic domain, hydrolase |
由来する生物種 | Homo sapiens (Human) |
細胞内の位置 | Nucleus: O95551 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 57789.33 |
構造登録者 | Hornyak, P.,Pearl, L.H.,Caldecott, K.W.,Oliver, A.W. (登録日: 2016-03-31, 公開日: 2016-05-04, 最終更新日: 2024-01-10) |
主引用文献 | Hornyak, P.,Askwith, T.,Walker, S.,Komulainen, E.,Paradowski, M.,Pennicott, L.E.,Bartlett, E.J.,Brissett, N.C.,Raoof, A.,Watson, M.,Jordan, A.M.,Ogilvie, D.J.,Ward, S.E.,Atack, J.R.,Pearl, L.H.,Caldecott, K.W.,Oliver, A.W. Mode of action of DNA-competitive small molecule inhibitors of tyrosyl DNA phosphodiesterase 2. Biochem.J., 473:1869-1879, 2016 Cited by PubMed Abstract: Tyrosyl-DNA phosphodiesterase 2 (TDP2) is a 5'-tyrosyl DNA phosphodiesterase important for the repair of DNA adducts generated by non-productive (abortive) activity of topoisomerase II (TOP2). TDP2 facilitates therapeutic resistance to topoisomerase poisons, which are widely used in the treatment of a range of cancer types. Consequently, TDP2 is an interesting target for the development of small molecule inhibitors that could restore sensitivity to topoisomerase-directed therapies. Previous studies identified a class of deazaflavin-based molecules that showed inhibitory activity against TDP2 at therapeutically useful concentrations, but their mode of action was uncertain. We have confirmed that the deazaflavin series inhibits TDP2 enzyme activity in a fluorescence-based assay, suitable for high-throughput screen (HTS)-screening. We have gone on to determine crystal structures of these compounds bound to a 'humanized' form of murine TDP2. The structures reveal their novel mode of action as competitive ligands for the binding site of an incoming DNA substrate, and point the way to generating novel and potent inhibitors of TDP2. PubMed: 27099339DOI: 10.1042/BCJ20160180 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (3.1 Å) |
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