Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

You are viewing the site in preview mode

Skip to main content
Fig. 4 | Retrovirology

Fig. 4

From: HIV-1 subtype C Nef-mediated SERINC5 down-regulation significantly contributes to overall Nef activity

Fig. 4

The relationship between dE0/dE90 values and SERINC5 down-regulation as well as viral load set point. SERINC5 down-regulation activity of patient-derived Nef clones (expressed relative to SF2 Nef, which represents 100% activity) correlated significantly (Spearman’s correlation) with dE0 values (A) and dE90 values (B), which are proxies for overall Nef function in vivo. dE0 values were derived from the Nef fitness landscape Ising model (only the consensus amino acid present at each residue was modelled explicitly) for each Nef clone, while dE90 values were derived from the Nef fitness landscape Potts model (each amino acid present at each residue was modelled explicitly) [17]. The dE0 values (C) and dE90 values (D) also correlated significantly with viral load set point (Spearman’s correlation)

Back to article page