Show simple item record

dc.contributor.authorSari, Yulia
dc.contributor.authorPrasetyo, Afiono Agung
dc.contributor.authorDesyardi, Martinus Nuherwan
dc.date.accessioned2012-04-25T04:15:54Z
dc.date.available2012-04-25T04:15:54Z
dc.date.issued2010-02
dc.identifier.citationAlter M. J. 2007. Epidemiology of hepatitis C infection. World Journal of Gastroenterology 13(17): 2436-41. Brohm C, Steinmann E, Friesland M, Lorenz IC, Patel A, Penin F, Bartenschlager R, Pietschmann T. 2009. Characterization of determinants important for hepatitis C virus p7 function in morphogenesis by using trans-complementation. J Virol 83(22): 11682-93. Chevaliez S. and Pawlotsky J. M. 2006. HCV genome and life cycle. In: Tan S. L. (ed). 2006. Hepatitis C Viruses: Genomes and Molecular Biology. Horizon Scientific Press. Cook GA, Opella SJ. 2010. NMR studies of p7 protein from hepatitis C virus. Eur Biophys J 39(7): 1097-104. Griffin S, Stgelais C, Owsianka AM, Patel AH, Rowlands D, Harris M. 2008. Genotype-dependent sensitivity of hepatitis C virus to inhibitors of the p7 ion channel. Hepatology core protein reveals numerous residues essential for production of infectious virus. J Virol 81(19): 10220-31. Russell RS, Meunier JC, Takikawa S, Faulk K, Engle RE, Bukh J, Purcell RH, Emerson SU. 2008. Advantages of a single-cycle production assay to study cell culture-adaptive mutations of hepatitis C virus. Proc Natl Acad Sci U S A 105(11): 4370-5. Steinmann E, Penin F, Kallis S, Patel AH, Bartenschlager R, Pietschmann T. 2007. Hepatitis C virus p7 protein is crucial for assembly and release of infectious virions. PLoS Pathog 3(7):e103. StGelais C, Foster TL, Verow M, Atkins E, Fishwick CW, Rowlands D, Harris M, Griffin S. 2009. Determinants of hepatitis C virus p7 ion channel function and drug sensitivity identified in vitro. J Virol 83(16): 7970-81. Tamura K, Dudley J, Nei M, Kumar S. 2007. MEGA4: Molecular Evolutionary Genetic Analysis (MEGA) software version 4.0. Mol Biol Evol 24: 1596-9. Thompson JD, Higgins DG, Gibson TJ. 1994. CLUSTAL W: improving the sensitivity of progressive multiple sequence aligment through sequence weighting, position-specific gap penalties and weight matrix choice. Nuc Acids Res 22 (22): 4673-80. Wozniak AL, Griffin S, Rowlands D, Harris M, Yi M, Lemon SM, Weinman SA. 2010. Intracellular proton conductance of the hepatitis C virus p7 protein and its contribution to infectious virus production. PLoS Pathog. 6(9):e1001087.en_US
dc.identifier.issn2085-8345
dc.identifier.urihttp://hdl.handle.net/11617/1003
dc.description.abstractThe hepatitis C virus (HCV) p7 protein is known essential for virus infection and replication. It exhibits ion-channel activity reported to be specifically blocked by various compounds, making it an attractive drug target. However, at present only little is known about the underlying molecular mechanisms of HCV p7. To predict and more understanding the molecular pattern of HCV p7 we cloned the p7 gene of HCV isolated in Central of Java Indonesia. The sequence results were then aligned with all of HCV 1a p7 complete coding sequences reported in GenBank. In total, 591 sequences were retrieved and aligned by ClustalW. We revealed the nucleotide and amino acid sequence consensus of HCV p7 gene. Overall, only aa 5, 12, 30, 34, 42, 48, 52, 58, and 63 were not have any variation. Amino acid variations may have relevant changes of physicochemical properties so that influence the replication efficiency, therefore, the amino acid variations found in the present report need further study.en_US
dc.subjectHCVen_US
dc.subjectp7en_US
dc.titleCloning and Molecular Analysis of HCVP7 Complete Coding Sequenceen_US
dc.typeArticleen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record