Klemm J D, Rould M A, Aurora R, Herr W, Pabo C O
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Cell. 1994 Apr 8;77(1):21-32. doi: 10.1016/0092-8674(94)90231-3.
The structure of an Oct-1 POU domain-octamer DNA complex has been solved at 3.0 A resolution. The POU-specific domain contacts the 5' half of this site (ATGCAAAT), and as predicted from nuclear magnetic resonance studies, the structure, docking, and contacts are remarkably similar to those of the lambda and 434 repressors. The POU homeodomain contacts the 3' half of this site (ATGCAAAT), and the docking is similar to that of the engrailed, MAT alpha 2, and Antennapedia homeodomains. The linker region is not visible and there are no protein-protein contacts between the domains, but overlapping phosphate contacts near the center of the octamer site may favor cooperative binding. This novel arrangement raises important questions about cooperativity in protein-DNA recognition.
已以3.0埃的分辨率解析了Oct-1 POU结构域-八聚体DNA复合物的结构。POU特异性结构域与该位点的5'半段(ATGCAAAT)接触,并且正如从核磁共振研究中预测的那样,其结构、对接和接触与λ和434阻遏物的结构、对接和接触非常相似。POU同源结构域与该位点的3'半段(ATGCAAAT)接触,其对接与engrailed、MAT α2和触角足同源结构域的对接相似。连接区域不可见,结构域之间没有蛋白质-蛋白质接触,但八聚体位点中心附近重叠的磷酸接触可能有利于协同结合。这种新的排列方式引发了关于蛋白质-DNA识别中协同作用的重要问题。