Crystal structure of the multidrug binding transcriptional repressor QacR bound to rhodamine 6G
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Crystal structure of the multidrug binding transcriptional repressor QacR bound to rhodamine 6G Descriptor: HYPOTHETICAL TRANSCRIPTIONAL REGULATOR IN QACA 5'REGION, RHODAMINE 6G, SULFATE ION Authors: Schumacher, M.A, Miller, M.C, Grkovic, S, Brown, M.H, Skurray, R.A, Brennan, R.G. Deposit date: 2001-08-27 Release date: 2001-12-12 Last modified: 2024-11-20 Method: X-RAY DIFFRACTION (2.84 Å) Cite: Structural mechanisms of QacR induction and multidrug recognition. Science, 294, 2001
多药结合转录阻遏蛋白QacR与罗丹明6G(rhodamine 6G)结合的晶体结构
描述:QACA 5'区域的假设型转录调控因子、罗丹明6G、硫酸根离子
作者:Schumacher, M.A.、Miller, M.C.、Grkovic, S.、Brown, M.H.、Skurray, R.A.、Brennan, R.G.
保藏日期:2001-08-27
发布日期:2001-12-12
最后更新日期:2024-11-20
实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率为2.84埃
引用文献:《QacR的诱导与多药识别的结构机制》,《科学》(Science),第294卷,2001年
创建时间:
2001-08-27



