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Bioinformatics analysis and construction of phylogenetic tree of aquaporins from Echinococcus granulosus

机译:细粒棘球a水通道蛋白的生物信息学分析及系统树构建

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摘要

Cyst echinococcosis caused by the matacestodal larvae of Echinococcus granulosus (Eg), is a chronic, worldwide, and severe zoonotic parasitosis. The treatment of cyst echinococcosis is still difficult since surgery cannot fit the needs of all patients, and drugs can lead to serious adverse events as well as resistance. The screen of target proteins interacted with new anti-hydatidosis drugs is urgently needed to meet the prevailing challenges. Here, we analyzed the sequences and structure properties, and constructed a phylogenetic tree by bioinformatics methods. The MIP family signature and Protein kinase C phosphorylation sites were predicted in all nine EgAQPs. alpha-helix and random coil were the main secondary structures of EgAQPs. The numbers of transmembrane regions were three to six, which indicated that EgAQPs contained multiple hydrophobic regions. A neighbor-joining tree indicated that EgAQPs were divided into two branches, seven EgAQPs formed a clade with AQP1 from human, a "strict" aquaporins, other two EgAQPs formed a clade with AQP9 from human, an aquaglyceroporins. Unfortunately, homology modeling of EgAQPs was aborted. These results provide a foundation for understanding and researches of the biological function of E. granulosus.
机译:由粒状棘球(虫(Echinococcus granulosus,Eg)的食虫幼虫引起的囊肿棘球co病是一种慢性的,全球性的,严重的人畜共患寄生虫病。由于手术不能满足所有患者的需求,因此仍然难以治疗囊虫包囊球菌病,药物可能导致严重的不良事件以及耐药性。迫切需要筛选与新的抗葡萄胎症药物相互作用的靶蛋白,以应对当前的挑战。在这里,我们分析了序列和结构特性,并通过生物信息学方法构建了系统发育树。在所有九个EgAQP中都预测了MIP家族特征和蛋白激酶C磷酸化位点。 α-螺旋和无规卷曲是EgAQPs的主要二级结构。跨膜区域的数目为3至6,这表明EgAQPs包含多个疏水区域。相邻的一棵树表明,EgAQPs分为两个分支,七个EgAQPs与人的AQP1形成了一个分支,一个“严格”水通道蛋白,另外两个EgAQPs与人的AQP9形成了一个分支,一个人是水性甘油甘油。不幸的是,EgAQPs的同源性建模被中止了。这些结果为理解和研究颗粒大肠杆菌的生物学功能提供了基础。

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