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Structural Comparative Analysis of Secreted NTPDase Models of Schistosoma mansoni and Homo sapiens

机译:曼氏血吸虫和智人分泌型NTPDase模型的结构比较分析

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The control of extracellular nucleoside concentrations by Nu-cleoside Triphosphate Diphosphohydrolase (NTPDase) is essential in the regulation of the purinergic signalling and also in immune response. In humans, eight members (HsNTPDase) were identified as transmembrane and secreted proteins. In Schistosoma mansoni, the causative agent of schistosomiasis, NTPDases similar to the humans enzymes have also been identified. The expression of these enzymes in S. mansoni (SmATPDases) is related to the weakening of the immune and inflammatory responses of the host against infections. Despite of the high phylogenetic conservation between these proteins, SmATPDases have been reported as molecular target candidates for antischistosomal treatment. In this work, we constructed three-dimensional models for secreted SmATPDase and HsNTPDase6, using comparative modeling technique. The comparative structural analysis aim the investigation of possible differences that could help future works in the development of new therapies that minimize the risk of cross inhibition.
机译:Nu-核苷三磷酸二磷酸水解酶(NTPDase)对胞外核苷浓度的控制在嘌呤能信号传导的调节以及免疫应答中至关重要。在人类中,八个成员(HsNTPDase)被鉴定为跨膜和分泌蛋白。在血吸虫病的病原体曼氏血吸虫中,还鉴定出了与人类酶相似的NTPDase。这些酶在曼氏链球菌中的表达(SmATPDases)与宿主抵抗感染的免疫和炎症反应减弱有关。尽管这些蛋白之间具有很高的系统发育保守性,但据报道SmATPDases是抗血吸虫病治疗的分子靶标候选物。在这项工作中,我们使用比较建模技术为分泌的SmATPDase和HsNTPDase6构建了三维模型。比较结构分析旨在研究可能的差异,这些差异可能有助于将来开发新疗法的工作,从而最大程度地降低交叉抑制的风险。

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