Exploration of the effect of sequence variations located inside the binding pocket of HIV-1 and HIV-2 proteases

HIV-2 protease (PR2) is naturally resistant to most FDA (Food and Drug Administration)-approved HIV-1 protease inhibitors (PIs), a major antiretroviral class. In this study, we compared the PR1 and PR2 binding pockets extracted from structures complexed with 12 ligands. The comparison of PR1 and PR2...

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Pubblicato in:Sci Rep
Autori principali: Triki, Dhoha, Billot, Telli, Visseaux, Benoit, Descamps, Diane, Flatters, Delphine, Camproux, Anne-Claude, Regad, Leslie
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2018
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5893546/
https://ncbi.nlm.nih.gov/pubmed/29636521
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-24124-5
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