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dc.contributor.authorAralaguppe, Shambhu Prasad G.
dc.contributor.authorSharma, Shilpee
dc.contributor.authorMenon, Malini
dc.contributor.authorPrasad, Vinayaka R.
dc.contributor.authorSaravanan, Shanmugam
dc.contributor.authorMurugavel, Kailapuri G.
dc.contributor.authorSolomon, Suniti
dc.contributor.authorRanga, Udaykumar
dc.date.accessioned2017-01-24T06:33:21Z-
dc.date.available2017-01-24T06:33:21Z-
dc.date.issued2016
dc.identifier.citationAralaguppe, S. P. G.; Sharma, S.; Menon, M.; Prasad, V. R.; Saravanan, S.; Murugavel, K. G.; Solomon, S.; Ranga, U., The Evolving Profile of the Signature Amino Acid Residues in HIV-1 Subtype C Tat. Aids Research and Human Retroviruses 2016, 32 (5), 503-514 http://dx.doi.org/10.1089/aid.2015.0208en_US
dc.identifier.citationAIDS Research and Human Retrovirusesen_US
dc.identifier.citation32en_US
dc.identifier.citation5en_US
dc.identifier.issn0889-2229
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/2193-
dc.descriptionRestricted Accessen_US
dc.description.abstractUsing several HIV-1 tat exon 1 amino acid sequences available from public databases and additional sequences derived from a southern Indian clinical cohort, we compared the profile of the signature amino acid residues (SAR) between two different time periods, 1986-2004 and 2005-2014. The analysis identified eight positions as signature residues in subtype C Tat and demonstrated a changing pattern at four of these positions between the two periods. At three locations (histidine 29, serine 57, and proline 60), there appears to be a nonuniform negative selection against the SAR. The negative selection appears to be severe, especially against histidine 29 (p<.0001) and moderate against proline 60 (p<.0001). The negative selection against serine 57 is statistically insignificant and appears to have begun recently. At position 63, the frequency of signature residue glutamic acid increased over the past decade, although the difference was not significant. Importantly, at the three locations where the negative selection is in progress, the substitute amino acids are the generic residues present in most of the other HIV-1 subtypes. Our data demonstrate that viral evolution can subject specific amino acid residues to subtle and progressive selection pressures without affecting the prevalence of other amino acid residues.en_US
dc.description.uri1931-8405en_US
dc.description.urihttp://dx.doi.org/10.1089/aid.2015.0208en_US
dc.language.isoEnglishen_US
dc.publisherMary Ann Liebert, Incen_US
dc.rights@Mary Ann Liebert, Inc, 2016en_US
dc.subjectImmunologyen_US
dc.subjectInfectious Diseasesen_US
dc.subjectVirologyen_US
dc.subjectHuman-Immunodeficiency-Virusen_US
dc.subjectClade-Specific Differencesen_US
dc.subjectMetal-Linked Dimeren_US
dc.subjectProteinen_US
dc.subjectType-1en_US
dc.subjectSequencesen_US
dc.subjectTransactivatoren_US
dc.subjectTranscriptionen_US
dc.subjectMonocytesen_US
dc.subjectMotifen_US
dc.titleThe Evolving Profile of the Signature Amino Acid Residues in HIV-1 Subtype C Taten_US
dc.typeArticleen_US
Appears in Collections:Research Papers (Udaykumar Ranga)

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