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Characterization and in silico proteomic analysis of C2 and C3 proteins of squash leaf curl China virus associated with pumpkin leaf curl disease in Assam, India

机译:南瓜叶卷曲中国病毒C2和C3蛋白的表征和硅蛋白质组学分析,印度南瓜叶卷曲疾病相关

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The pumpkin leaf curl disease is an emerging disease of pumpkin in Assam, India. Symptomatic pumpkin leaf samples from different locations were immunologically tested using Begomovirus specific antibody. PCR with the ELISA-positive samples, using Geminivirus universal primers amplified 1.4 kb virus-specific fragments. Sequence of these amplicons showed around 95% identity with squash leaf curl China virus-[Pumpkin: Varanasi] (SLCCV-Pumpkin: Varanasi EU573715). To investigate the possible functions of the viral proteins present in the fragment, the full-length C2 and C3 genes were conceptually translated and were subjected to in silico proteomic analyses. The phylogenetic analysis of both the proteins divulged the relationship of our isolate with related viruses and isolates. Multiple sequence alignment (MSA) of the proteins revealed the presence of the known viral conserved motifs, viz., zinc-finger (ZNF) motif [36CXCX(7) CX(6) H-53], the arginine-rich nuclear localization signal (NLS) motif (28RRRR31) as well as the minimal activation domain in C2 protein. In the C3 protein, the 91LKYLD95 and the replication enhancer motif (30YFK32) were found to be conserved. Finally, 3-D models of the two proteins were predicted via ab initio approach and subsequently, the models were validated. To our knowledge, this study is a pioneering attempt to construct the ab initio 3-D models of two begomoviral proteins taking a SLCCV isolate as a model.
机译:南瓜叶卷曲疾病是印度阿萨姆斯南瓜的新出现疾病。来自不同位置的症状南瓜样品使用Begomovirus特异性抗体免疫测试。使用ELISA阳性样品的PCR,使用Geminivirus Universal引物扩增1.4kb病毒特异性片段。这些扩增子的序列显示大约95%的身份与南瓜卷曲中国病毒 - [南瓜:varanasi](Slccv-南瓜:varanasi Eu573715)。为了研究片段中存在的病毒蛋白的可能功能,概念性翻译全长C2和C3基因并进行硅蛋白质组学分析。两种蛋白质的系统发育分析泄露了与相关病毒和分离株的孤立的关系。蛋白质的多个序列对准(MSA)显示出已知的病毒保守基序,VIZ,锌 - 手指(ZNF)基序[36CXCX(7)CX(6)H-53],富含精氨酸的核定位信号(NLS)基序(28RRRR31)以及C2蛋白中的最小活化结构域。在C3蛋白中,发现91lkyld95和复制增强剂基序(30YFK32)被保守。最后,通过AB Initio方法预测了两种蛋白质的3D模型,随后,验证了模型。据我们所知,该研究是构建两种前对象蛋白的AB Initio 3-D模型的开创性尝试,其占SLCCV分离为模型。

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