Mohanty Smita, Srinivasan N
Molecular Biophysics Unit, Indian Institute of Science, Bangalore-560012, India.
Protein Pept Lett. 2009;16(8):961-8. doi: 10.2174/092986609788923257.
The genome of Plasmodium falciparum, a malarial parasite, is atypical as many of the encoded proteins have diverged extensively from their homologues in other organisms. Hence homology-based information transfer is not entirely successful and presently, proper function annotation is unavailable for over 50% of the proteome. It has been hypothesized that enzymes participating in nearly 69 metabolic steps are not yet identified. In this paper we report detection of some of the "missing metabolic enzymes" of P. falciparum. Our approach for remote homology detection to recognize the "missing" P. falciparum enzymes employs multiple profiles for every protein domain family. A blind assessment of the approach to recognize known metabolic proteins of P. falciparum resulted in 94% success rate. Using this approach we have successfully recognized 14 of the "missing" enzymes. Results of protein fold recognition and information from microarray and protein-protein interaction datasets are consistent with our predictions. In a few cases we also provide the list of functionally important residues extrapolated on the basis of homology.
恶性疟原虫是一种疟疾寄生虫,其基因组具有非典型性,因为许多编码蛋白与其他生物体中的同源物相比已经发生了广泛的分化。因此,基于同源性的信息传递并不完全成功,目前,超过50%的蛋白质组无法进行正确的功能注释。据推测,参与近69个代谢步骤的酶尚未被鉴定出来。在本文中,我们报告了对恶性疟原虫一些“缺失的代谢酶”的检测。我们用于远程同源性检测以识别恶性疟原虫“缺失”酶的方法,对每个蛋白质结构域家族采用多个谱。对识别恶性疟原虫已知代谢蛋白的方法进行的盲测成功率为94%。使用这种方法,我们成功识别了14种“缺失”的酶。蛋白质折叠识别结果以及来自微阵列和蛋白质 - 蛋白质相互作用数据集的信息与我们的预测一致。在少数情况下,我们还提供了基于同源性推断出的功能重要残基列表。