Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
J Struct Biol. 2013 Feb;181(2):185-9. doi: 10.1016/j.jsb.2012.11.001. Epub 2012 Nov 16.
Acetate kinases (ACKs) are members of the acetate and sugar kinase/hsp70/actin (ASKHA) superfamily and catalyze the reversible phosphorylation of acetate, with ADP/ATP the most common phosphoryl acceptor/donor. While prokaryotic ACKs have been the subject of extensive biochemical and structural characterization, there is a comparative paucity of information on eukaryotic ACKs, and prior to this report, no structure of an ACK of eukaryotic origin was available. We determined the structures of ACKs from the eukaryotic pathogens Entamoeba histolytica and Cryptococcus neoformans. Each active site is located at an interdomain interface, and the acetate and phosphate binding pockets display sequence and structural conservation with their prokaryotic counterparts. Interestingly, the E. histolytica ACK has previously been shown to be pyrophosphate (PP(i))-dependent, and is the first ACK demonstrated to have this property. Examination of its structure demonstrates how subtle amino acid substitutions within the active site have converted cosubstrate specificity from ATP to PP(i) while retaining a similar backbone conformation. Differences in the angle between domains surrounding the active site suggest that interdomain movement may accompany catalysis. Taken together, these structures are consistent with the eukaryotic ACKs following a similar reaction mechanism as is proposed for the prokaryotic homologs.
乙酰激酶 (ACK) 是乙酸盐和糖激酶/hsp70/肌动蛋白 (ASKHA) 超家族的成员,可催化乙酸盐的可逆磷酸化,其中 ADP/ATP 是最常见的磷酸化供体/受体。虽然原核 ACK 已经进行了广泛的生化和结构表征,但关于真核 ACK 的信息相对较少,在此报告之前,尚无真核起源的 ACK 结构。我们测定了真核病原体溶组织内阿米巴原虫和新生隐球菌的 ACK 结构。每个活性位点都位于结构域界面之间,并且乙酸盐和磷酸盐结合口袋在序列和结构上与原核对应物保持一致。有趣的是,先前已经表明溶组织内阿米巴原虫的 ACK 依赖焦磷酸盐 (PP(i)),并且是第一个具有这种特性的 ACK。对其结构的检查表明,活性位点内的微小氨基酸取代如何将共底物特异性从 ATP 转换为 PP(i),同时保持类似的骨架构象。围绕活性位点的结构域之间角度的差异表明,结构域间的运动可能伴随催化作用。总之,这些结构与真核 ACK 遵循与原核同源物提出的类似反应机制一致。