Institute for Pharmacology and Toxicology, University of Würzburg, Versbacher Strasse 9, D-97078 Würzburg, Germany.
Biochim Biophys Acta Mol Cell Res. 2019 Jan;1866(1):153-166. doi: 10.1016/j.bbamcr.2018.07.007. Epub 2018 Jul 18.
Mammalian haloacid dehalogenase (HAD)-type phosphatases have evolved to dephosphorylate a wide range of small metabolites, but can also target macromolecules such as serine/threonine, tyrosine-, and histidine-phosphorylated proteins. To accomplish these tasks, HAD phosphatases are equipped with cap domains that control access to the active site and provide substrate specificity determinants. A number of capped HAD phosphatases impact protein phosphorylation, although structural data are consistent with small metabolite substrates rather than protein substrates. This review discusses the structures, functions and disease implications of the three closely related, capped HAD phosphatases pyridoxal phosphatase (PDXP or chronophin), phosphoglycolate phosphatase (PGP, also termed AUM or glycerol phosphatase) and phospholysine phosphohistidine inorganic pyrophosphate phosphatase (LHPP or HDHD2B). Evidence in support of small metabolite and protein phosphatase activity is discussed in the context of the diversity of their biological functions.
哺乳动物卤酸脱卤酶 (HAD)-型磷酸酶已进化为能够去磷酸化广泛的小分子代谢物,但也可以靶向丝氨酸/苏氨酸、酪氨酸和组氨酸磷酸化蛋白等大分子。为了完成这些任务,HAD 磷酸酶配备了帽结构域,这些结构域控制着对活性位点的访问,并提供了底物特异性决定因素。许多带帽的 HAD 磷酸酶会影响蛋白质磷酸化,尽管结构数据与小分子代谢物底物而非蛋白质底物一致。这篇综述讨论了三种密切相关的带帽 HAD 磷酸酶——吡哆醛磷酸酶 (PDXP 或 chronophin)、磷酸甘油酸磷酸酶 (PGP,也称为 AUM 或甘油磷酸酶) 和磷酸多赖氨酸磷酸组氨酸无机焦磷酸磷酸酶 (LHPP 或 HDHD2B) 的结构、功能和疾病意义。本文还讨论了它们的生物功能多样性背景下的小分子和蛋白质磷酸酶活性的证据。