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Analytical Study of Plasmodium Yoelii Yoelii

机译:疟原虫Yoelii Yoelii的分析研究

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Protein sequence of Plasmodium yoelii yoelii "prt_seq No definition line found" was extracted from GenPept database (ACCESSION: EAA21357), used to predict its hydrophobic, atomic and amino acid composition, PEST region, solvent accessibility, molecular mass, theoretical pI and finally catalytic site detail was identified with their three dimensional structure. Analysis was made using several bioinformatics tool. PEST region was indentified using pestfind tool, whose abundant availability indicates intracellular half-lives of less than two hour. Hydrophobicity was checked using [1] to know it's buried or exposed state in terms of solvent accessibility, also used to find its different physical and chemical properties, secondary structure composition using Hidden Markov models, formation of disulphide bond, effect of point mutation prediction using heat map representation and finally catalytic site identification were made. Online Active site prediction was made using web server [2], where given protein sequence was matched with server's library of catalytic site, resulting in twenty six identified region with maximum score of 0.015 with Orotidine "5-monophosphate decarboxylase" and minimum score of 0.004 with "Endo-alpha-sialidase". Molecular weight of retrieved protein sequence was found to be 32049.9 and Theoretical Pi value was 6.08, protein close to given Pi and molecular mass was matched using TagIdent web server [3], which reveal 126466 protein. The Instability Index was computed to be 36.19 which classifies the protein as stable and the Aliphatic Index showing relative value occupied by aliphatic side chain (alanine, valine, isoleucine, and leucine) was 80.77. The three dimensional structure of catalytic site was visualized using Jmol software.
机译:从GenPept数据库(ACCESSION:EAA21357)中提取约氏疟原虫的蛋白质序列“ prt_seq No definition line found”,用于预测其疏水性,原子和氨基酸组成,PEST区域,溶剂可及性,分子量,理论pI并最终催化站点的详细信息由其三维结构确定。使用几种生物信息学工具进行了分析。使用害虫发现工具鉴定了PEST区域,该工具的丰富可用性表明其细胞内半衰期少于2小时。使用[1]检查疏水性,以了解其在溶剂可及性方面的掩埋或暴露状态,还用于发现其不同的物理和化学性质,使用隐马尔可夫模型的二级结构组成,二硫键的形成,使用点突变预测的效果进行热图表示,最后确定催化部位。使用Web服务器[2]进行在线活动位点预测,其中给定的蛋白质序列与服务器的催化位点库相匹配,从而产生26个已鉴定的区域,其中Orotidine“ 5-一磷酸脱羧酶”的最大得分为0.015,最小得分为0.004与“内切α-唾液酸酶”。检索到的蛋白质序列的分子量为32049.9,理论Pi值为6.08,接近给定Pi的蛋白质,使用TagIdent Web服务器对分子量进行匹配[3],可显示126466蛋白质。计算出的不稳定性指数为36.19,分类为稳定蛋白质,而显示脂肪族侧链(丙氨酸,缬氨酸,异亮氨酸和亮氨酸)相对值的脂肪指数为80.77。使用Jmol软件可视化催化位点的三维结构。

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