Butts Carter T, Bierma Jan C, Martin Rachel W
Department of Electrical Engineering and Computer Science, UC Irvine, Irvine, California, 92697.
Department of Statistics, UC Irvine, Irvine, California, 92697.
Proteins. 2016 Oct;84(10):1517-33. doi: 10.1002/prot.25095. Epub 2016 Jul 13.
In his 1875 monograph on insectivorous plants, Darwin described the feeding reactions of Drosera flypaper traps and predicted that their secretions contained a "ferment" similar to mammalian pepsin, an aspartic protease. Here we report a high-quality draft genome sequence for the cape sundew, Drosera capensis, the first genome of a carnivorous plant from order Caryophyllales, which also includes the Venus flytrap (Dionaea) and the tropical pitcher plants (Nepenthes). This species was selected in part for its hardiness and ease of cultivation, making it an excellent model organism for further investigations of plant carnivory. Analysis of predicted protein sequences yields genes encoding proteases homologous to those found in other plants, some of which display sequence and structural features that suggest novel functionalities. Because the sequence similarity to proteins of known structure is in most cases too low for traditional homology modeling, 3D structures of representative proteases are predicted using comparative modeling with all-atom refinement. Although the overall folds and active residues for these proteins are conserved, we find structural and sequence differences consistent with a diversity of substrate recognition patterns. Finally, we predict differences in substrate specificities using in silico experiments, providing targets for structure/function studies of novel enzymes with biological and technological significance. Proteins 2016; 84:1517-1533. © 2016 Wiley Periodicals, Inc.
在1875年关于食虫植物的专著中,达尔文描述了茅膏菜捕蝇器的捕食反应,并预测其分泌物中含有一种类似于哺乳动物胃蛋白酶(一种天冬氨酸蛋白酶)的“发酵剂”。在此,我们报告了好望角茅膏菜(Drosera capensis)的高质量基因组草图序列,这是石竹目食肉植物的首个基因组,石竹目还包括捕蝇草(捕蝇草属)和热带猪笼草(猪笼草属)。选择该物种部分是因其耐寒且易于栽培,使其成为进一步研究植物食肉性的优秀模式生物。对预测的蛋白质序列进行分析,得到了与其他植物中发现的蛋白酶同源的编码基因,其中一些显示出暗示新功能的序列和结构特征。由于在大多数情况下,与已知结构蛋白质的序列相似性太低,无法进行传统的同源建模,因此使用全原子精修的比较建模来预测代表性蛋白酶的三维结构。尽管这些蛋白质的整体折叠和活性残基是保守的,但我们发现结构和序列差异与多种底物识别模式一致。最后,我们通过计算机实验预测底物特异性的差异,为具有生物学和技术意义的新型酶的结构/功能研究提供靶点。《蛋白质》2016年;84:1517 - 1533。©2016威利期刊公司。