Analysis of sequence diversity and selection pressure in HIV-1 clade C gp41 from India
Author:
Funder
Department of Biotechnology, Government of India
Publisher
Springer Science and Business Media LLC
Subject
Infectious Diseases,Virology
Link
https://link.springer.com/content/pdf/10.1007/s13337-020-00595-x.pdf
Reference49 articles.
1. Agnihotri KD, Tripathy SP, Jere AP, Kale SM, Paranjape RS. Molecular analysis of gp41 sequences of HIV type 1 subtype C from India. J Acquir Immune Defic Syndr. 2006;41:345–51.
2. Bachu M, Yalla S, Asokan M, Verma A, Neogi U, Sharma S, et al. Multiple NF-κB sites in HIV-1 subtype C long terminal repeat confer superior magnitude of transcription and thereby the enhanced viral predominance. J Biol Chem. 2012;287:44714–35.
3. Bandawe GP, Martin DP, Treurnicht F, Mlisana K, Karim SSA, Williamson C, et al. Conserved positive selection signals in gp41 across multiple subtypes and difference in selection signals detectable in gp41 sequences sampled during acute and chronic HIV-1 subtype C infection. Virol J. 2008;5:141.
4. Bellamy-McIntyre AK, Lay C-S, Baär S, Maerz AL, Talbo GH, Drummer HE, et al. Functional links between the fusion peptide-proximal polar segment and membrane-proximal region of human immunodeficiency virus gp41 in distinct phases of membrane fusion. J Biol Chem. 2007;282:23104–16.
5. Blumenthal R, Durell S, Viard M. HIV entry and envelope glycoprotein-mediated fusion. J Biol Chem. 2012;287:40841–9.
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