Department of Molecular and Cellular Biology, University of Connecticut, Storrs, CT 06269, USA.
Biochemistry. 2012 Sep 4;51(35):6932-41. doi: 10.1021/bi300922z. Epub 2012 Aug 21.
Receiver domains control intracellular responses triggered by signal transduction in bacterial two-component systems. Here, we report the solution nuclear magnetic resonance structure and dynamics of Sma0114 from the bacterium Sinorhizobium meliloti, the first such characterization of a receiver domain from the HWE-kinase family of two-component systems. The structure of Sma0114 adopts a prototypical α(5)/β(5) Rossman fold but has features that set it apart from other receiver domains. The fourth β-strand of Sma0114 houses a PFxFATGY sequence motif, common to many HWE-kinase-associated receiver domains. This sequence motif in Sma0114 may substitute for the conserved Y-T coupling mechanism, which propagates conformational transitions in the 455 (α4-β5-α5) faces of receiver domains, to prime them for binding downstream effectors once they become activated by phosphorylation. In addition, the fourth α-helix of the consensus 455 face in Sma0114 is replaced with a segment that shows high flexibility on the pico- to nanosecond time scale by (15)N relaxation data. Secondary structure prediction analysis suggests that the absence of helix α4 may be a conserved property of the HWE-kinase-associated family of receiver domains to which Sma0114 belongs. In spite of these differences, Sma0114 has a conserved active site, binds divalent metal ions such as Mg(2+) and Ca(2+) that are required for phosphorylation, and exhibits micro- to millisecond active-site dynamics similar to those of other receiver domains. Taken together, our results suggest that Sma0114 has a conserved active site but differs from typical receiver domains in the structure of the 455 face that is used to effect signal transduction following activation.
受体结构域控制细菌双组分系统信号转导引发的细胞内反应。在这里,我们报告了来自根瘤菌 Sinorhizobium meliloti 的 Sma0114 的溶液核磁共振结构和动力学,这是第一个对 HWE-激酶家族双组分系统的受体结构域进行这样的描述。Sma0114 的结构采用了典型的α(5)/β(5)Rossman 折叠,但具有使其与其他受体结构域区分开来的特征。Sma0114 的第四β-链包含一个 PFxFATGY 序列基序,这是许多 HWE-激酶相关受体结构域所共有的。Sma0114 中的这个序列基序可能替代保守的 Y-T 偶联机制,该机制在受体结构域的 455(α4-β5-α5)面上传播构象转变,一旦它们被磷酸化激活,就为它们与下游效应物结合做好准备。此外,Sma0114 中共识 455 面的第四α-螺旋被一个在皮秒到纳秒时间尺度上表现出高灵活性的片段所取代,这是通过 (15)N 弛豫数据得出的。二级结构预测分析表明,α4 螺旋的缺失可能是 Sma0114 所属的 HWE-激酶相关受体家族的一个保守特性。尽管存在这些差异,Sma0114 具有保守的活性位点,结合二价金属离子(如 Mg(2+)和 Ca(2+)),这些金属离子是磷酸化所必需的,并且表现出与其他受体结构域相似的微秒到毫秒的活性位点动力学。总之,我们的结果表明,Sma0114 具有保守的活性位点,但在 455 面的结构上与典型的受体结构域不同,该结构域在激活后用于信号转导。