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Predicting the host protein interactors of Chandipura virus using a structural similarity–based approach

机译:预测蛋白质扶少团团员使用结构Chandipura病毒相似性的方法

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摘要

Chandipura virus (CHPV), alike other pathogens, exploits the cellular infrastructure of their hosts through complex network of interactions for successful infection. CHPV being a recently emerged pediatric encephalitic virus, the mechanisms involved in the establishment of viral persistence are still ill defined. Because the protein interface between CHPV and its host provides one means by which the virus invades and seize control of their human host machinery, the authors in this study have employed computational methods to create a network of putative protein–protein interactions between CHPV and its human host to shed light on the hitherto less-known CHPV biology. On the basis of the 2105 potential interactions predicted among 1650 human proteins and the five proteins of CHPV, the authors decipher the probable mode by which the virus manipulates the biological pathways of its host toward its own end and replicates while evading the immune system. Identification of such conserved set of putative interactions that allow the virus to take control of the host has the potential to deepen our understanding of the virus-specific remodeling processes of the host cell and illuminate new arenas of disease intervention.
机译:Chandipura病毒(CHPV)相似的其他病原体,利用细胞的基础设施主机通过复杂网络的交互成功的感染。小儿出现脑炎的病毒机制的建立病毒持久性仍然是不清楚的。蛋白质CHPV和主机之间的接口病毒侵入和提供了一种手段控制他们的人类宿主机器,作者在本研究中采用计算方法来创建一个假定的网络蛋白质CHPV及其之间的相互作用人类宿主阐明迄今为止不知名的CHPV生物学。潜在的相互作用预测在1650人CHPV蛋白质和五个蛋白质,作者解释的可能模式病毒操纵的生物学途径主持人对自己的结束和复制逃避免疫系统。保存设置允许的假定的交互病毒控制主机的潜在的加深我们的了解特异主机的重构过程细胞和阐明疾病的新领域干预。

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