School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ, U.K.
Department of Biology, School of Life Sciences, Southern University of Science and Technology, Nanshan, Shenzhen 518055, China.
Biochem J. 2023 Mar 29;480(6):433-453. doi: 10.1042/BCJ20220579.
Myo-inositol tris/tetrakisphosphate kinases (ITPKs) catalyze diverse phosphotransfer reactions with myo-inositol phosphate and myo-inositol pyrophosphate substrates. However, the lack of structures of nucleotide-coordinated plant ITPKs thwarts a rational understanding of phosphotransfer reactions of the family. Arabidopsis possesses a family of four ITPKs of which two isoforms, ITPK1 and ITPK4, control inositol hexakisphosphate and inositol pyrophosphate levels directly or by provision of precursors. Here, we describe the specificity of Arabidopsis ITPK4 to pairs of enantiomers of diverse inositol polyphosphates and show how substrate specificity differs from Arabidopsis ITPK1. Moreover, we provide a description of the crystal structure of ATP-coordinated AtITPK4 at 2.11 Å resolution that, along with a description of the enantiospecificity of the enzyme, affords a molecular explanation for the diverse phosphotransferase activity of this enzyme. That Arabidopsis ITPK4 has a KM for ATP in the tens of micromolar range, potentially explains how, despite the large-scale abolition of InsP6, InsP7 and InsP8 synthesis in Atitpk4 mutants, Atitpk4 lacks the phosphate starvation responses of Atitpk1 mutants. We further demonstrate that Arabidopsis ITPK4 and its homologues in other plants possess an N-terminal haloacid dehalogenase-like fold not previously described. The structural and enzymological information revealed will guide elucidation of ITPK4 function in diverse physiological contexts, including InsP8-dependent aspects of plant biology.
肌醇三磷酸/四磷酸激酶(ITPKs)催化各种磷酸转移反应,涉及肌醇磷酸盐和肌醇焦磷酸盐底物。然而,由于缺乏核苷酸配位的植物 ITPK 的结构,阻碍了对该家族磷酸转移反应的合理理解。拟南芥拥有一个四聚体 ITPK 家族,其中两个同工酶 ITPK1 和 ITPK4 直接或通过提供前体来控制肌醇六磷酸和肌醇焦磷酸水平。在这里,我们描述了拟南芥 ITPK4 对各种肌醇多磷酸盐对映异构体的特异性,并展示了其底物特异性如何与拟南芥 ITPK1 不同。此外,我们提供了与酶的对映体特异性相关的 ATP 配位的 AtITPK4 的晶体结构描述,分辨率为 2.11 Å,这与酶的多样化磷酸转移酶活性的描述一起,为该酶的不同磷酸转移酶活性提供了分子解释。拟南芥 ITPK4 对 ATP 的 KM 值在数十微摩尔范围内,这可能解释了为什么尽管 Atitpk4 突变体中大规模消除了 InsP6、InsP7 和 InsP8 的合成,但 Atitpk4 缺乏 Atitpk1 突变体的磷酸盐饥饿反应。我们进一步证明,拟南芥 ITPK4 及其在其他植物中的同源物具有以前未描述的 N 端卤代酸脱卤酶样折叠。揭示的结构和酶学信息将指导阐明 ITPK4 在各种生理环境中的功能,包括植物生物学中依赖 InsP8 的方面。