8C4M
CdaA-Adenosine complex
8C4M の概要
エントリーDOI | 10.2210/pdb8c4m/pdb |
分子名称 | Diadenylate cyclase, ADENOSINE, CHLORIDE ION, ... (4 entities in total) |
機能のキーワード | complex, protein binding |
由来する生物種 | Listeria monocytogenes |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 39111.80 |
構造登録者 | |
主引用文献 | Neumann, P.,Kloskowski, P.,Ficner, R. Computer-aided design of a cyclic di-AMP synthesizing enzyme CdaA inhibitor. Microlife, 4:uqad021-uqad021, 2023 Cited by PubMed Abstract: Cyclic di-AMP (c-di-AMP) is an essential secondary messenger regulating cell wall homeostasis and myriads of physiological processes in several Gram-positive and mycobacteria, including human pathogens. Hence, c-di-AMP synthesizing enzymes (DACs) have become a promising antibacterial drug target. To overcome a scarcity of small molecule inhibitors of c-di-AMP synthesizing enzyme CdaA, a computer-aided design of a new compound that should block the enzyme has been performed. This has led to the identification of a molecule comprising two thiazole rings and showing inhibitory potential based on ITC measurements. Thiazole scaffold is a good pharmacophore nucleus known due to its various pharmaceutical applications. It is contained in more than 18 FDA-approved drugs as well as in dozens of experimental drugs. Hence, the designed inhibitor can serve as a potent lead compound for further development of inhibitor against CdaA. PubMed: 37223749DOI: 10.1093/femsml/uqad021 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.51 Å) |
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