Warsaw University of Life Sciences, Warsaw, Poland.
PLoS One. 2012;7(2):e32138. doi: 10.1371/journal.pone.0032138. Epub 2012 Feb 16.
Selenoproteins serve important functions in many organisms, usually providing essential oxidoreductase enzymatic activity, often for defense against toxic xenobiotic substances. Most eukaryotic genomes possess a small number of these proteins, usually not more than 20. Selenoproteins belong to various structural classes, often related to oxidoreductase function, yet a few of them are completely uncharacterised.Here, the structural and functional prediction for the uncharacterised selenoprotein O (SELO) is presented. Using bioinformatics tools, we predict that SELO protein adopts a three-dimensional fold similar to protein kinases. Furthermore, we argue that despite the lack of conservation of the "classic" catalytic aspartate residue of the archetypical His-Arg-Asp motif, SELO kinases might have retained catalytic phosphotransferase activity, albeit with an atypical active site. Lastly, the role of the selenocysteine residue is considered and the possibility of an oxidoreductase-regulated kinase function for SELO is discussed.The novel kinase prediction is discussed in the context of functional data on SELO orthologues in model organisms, FMP40 a.k.a.YPL222W (yeast), and ydiU (bacteria). Expression data from bacteria and yeast suggest a role in oxidative stress response. Analysis of genomic neighbourhoods of SELO homologues in the three domains of life points toward a role in regulation of ABC transport, in oxidative stress response, or in basic metabolism regulation. Among bacteria possessing SELO homologues, there is a significant over-representation of aquatic organisms, also of aerobic ones. The selenocysteine residue in SELO proteins occurs only in few members of this protein family, including proteins from Metazoa, and few small eukaryotes (Ostreococcus, stramenopiles). It is also demonstrated that enterobacterial mchC proteins involved in maturation of bactericidal antibiotics, microcins, form a distant subfamily of the SELO proteins.The new protein structural domain, with a putative kinase function assigned, expands the known kinome and deserves experimental determination of its biological role within the cell-signaling network.
硒蛋白在许多生物体中具有重要功能,通常提供必需的氧化还原酶酶活性,通常用于抵御有毒的异生物质。大多数真核生物基因组拥有少量这些蛋白质,通常不超过 20 个。硒蛋白属于各种结构类别,通常与氧化还原酶功能有关,但其中一些完全没有特征。在这里,呈现了未表征的硒蛋白 O(SELO)的结构和功能预测。使用生物信息学工具,我们预测 SELO 蛋白采用类似于蛋白激酶的三维折叠。此外,我们认为尽管缺乏典型的 His-Arg-Asp 基序中“经典”催化天冬氨酸残基的保守性,但 SELO 激酶可能保留了催化磷酸转移酶活性,尽管具有非典型的活性位点。最后,考虑了硒代半胱氨酸残基的作用,并讨论了 SELO 的氧化还原酶调节激酶功能的可能性。在模型生物中,FMP40(酵母)和 ydiU(细菌)的 SELO 同源物的功能数据的背景下讨论了新型激酶的预测。来自细菌和酵母的表达数据表明其在氧化应激反应中起作用。对生命三个域中 SELO 同源物的基因组邻近区域的分析表明其在 ABC 转运、氧化应激反应或基本代谢调节中的作用。在具有 SELO 同源物的细菌中,水生生物和需氧生物的数量显著增加。SELO 蛋白中的硒代半胱氨酸残基仅存在于该蛋白质家族的少数成员中,包括来自后生动物门和少数小型真核生物(Ostreococcus,Stramenopiles)的蛋白质。还证明了参与杀菌抗生素、微菌素成熟的肠杆菌 mchC 蛋白形成 SELO 蛋白的一个遥远的亚家族。具有假定激酶功能的新蛋白质结构域扩展了已知的激酶组,值得在细胞信号网络中对其生物学作用进行实验确定。