7UDP
Crystal structure of COQ8A-CA157 inhibitor complex in space group C2
7UDP の概要
| エントリーDOI | 10.2210/pdb7udp/pdb |
| 分子名称 | Atypical kinase COQ8A, mitochondrial, 4-[(3,4,5-trimethoxyphenyl)amino]quinoline-7-carbonitrile (3 entities in total) |
| 機能のキーワード | coq biosynthesis, kinase-like, transferase |
| 由来する生物種 | Homo sapiens (human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 45583.32 |
| 構造登録者 | Bingman, C.A.,Murray, N.,Smith, R.W.,Pagliarini, D.J. (登録日: 2022-03-20, 公開日: 2023-01-18, 最終更新日: 2023-10-25) |
| 主引用文献 | Murray, N.H.,Asquith, C.R.M.,Fang, Z.,East, M.P.,Ptak, N.,Smith, R.W.,Vasta, J.D.,Zimprich, C.A.,Corona, C.R.,Robers, M.B.,Johnson, G.L.,Bingman, C.A.,Pagliarini, D.J. Small-molecule inhibition of the archetypal UbiB protein COQ8. Nat.Chem.Biol., 19:230-238, 2023 Cited by PubMed Abstract: Small-molecule tools have enabled mechanistic investigations and therapeutic targeting of the protein kinase-like (PKL) superfamily. However, such tools are still lacking for many PKL members, including the highly conserved and disease-related UbiB family. Here, we sought to develop and characterize an inhibitor for the archetypal UbiB member COQ8, whose function is essential for coenzyme Q (CoQ) biosynthesis. Guided by crystallography, activity assays and cellular CoQ measurements, we repurposed the 4-anilinoquinoline scaffold to selectively inhibit human COQ8A in cells. Our chemical tool promises to lend mechanistic insights into the activities of these widespread and understudied proteins and to offer potential therapeutic strategies for human diseases connected to their dysfunction. PubMed: 36302899DOI: 10.1038/s41589-022-01168-3 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.01 Å) |
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