Malopolska Centre of Biotechnology (MCB), Jagiellonian University, Krakow, Poland.
Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.
Curr Genet. 2020 Aug;66(4):823-833. doi: 10.1007/s00294-020-01070-2. Epub 2020 Mar 31.
Kti12 (Kluyveromyces lactis toxin insensitive 12) is an evolutionary highly conserved ATPase, crucial for the tRNA-modification activity of the eukaryotic Elongator complex. The protein consists of an N-terminal ATPase and a C-terminal tRNA-binding domain, which are connected by a flexible linker. The precise role of the linker region and its involvement in the communication between the two domains and their activities remain elusive. Here, we analyzed all available Kti12 protein sequences and report the discovery of a subset of Kti12 proteins with abnormally long linker regions. These Kti12 proteins are characterized by a co-occurring lysine to leucine substitution in their Walker A motif, previously thought to be invariable. We show that the K14L substitution lowers the affinity to ATP, but does not affect the catalytic activity of Kti12 at high ATP concentrations. We compare the activity of mutated variants of Kti12 in vitro with complementation assays in vivo in yeast. Ultimately, we compared Kti12 to other known p-loop ATPase family members known to carry a similar deviant Walker A motif. Our data establish Kti12 of Eurotiomycetes as an example of eukaryotic ATPase harboring a significantly deviating but still functional Walker A motif.
Kti12(乳克鲁维酵母毒素不敏感 12)是一种进化上高度保守的 ATP 酶,对真核延伸因子复合物的 tRNA 修饰活性至关重要。该蛋白由 N 端 ATP 酶和 C 端 tRNA 结合结构域组成,它们通过柔性接头连接。接头区域的确切作用及其在两个结构域之间的通讯及其活性中的作用仍然难以捉摸。在这里,我们分析了所有可用的 Kti12 蛋白序列,并报告了一组具有异常长接头区域的 Kti12 蛋白的发现。这些 Kti12 蛋白的特征是其 Walker A 基序中的赖氨酸到亮氨酸取代,以前认为是不变的。我们表明,K14L 取代降低了与 ATP 的亲和力,但不影响高 ATP 浓度下 Kti12 的催化活性。我们比较了 Kti12 在体外的突变变体的活性与酵母体内的互补测定。最终,我们将 Kti12 与其他已知的携带类似异常 Walker A 基序的 p 环 ATP 酶家族成员进行了比较。我们的数据将 Eurotiomycetes 的 Kti12 确立为具有明显偏离但仍然具有功能的 Walker A 基序的真核 ATP 酶的一个例子。