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. 2020 Oct 26;12(12):2403–2416. doi: 10.1093/gbe/evaa226

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© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Fig. 2 — Clustal-W analysis of the expanded salivarian RAC clades. Some clades containing sequences of T. evansi and T. congolense are collapsed. RACs with translational efficiency values retrieved from Vasquez et al. and selected for endogenous tagging of T. brucei procyclics are indicated in bold. The support values are in the following format: SH-aLRT support (%)/bootstrap support (%). Only support values ≥50% are shown. Flagellum-localized RACs (ACP1 thru 6) described by Saada et al. (2014) are in brackets. Shaded boxes represent distinct chromosomes indicated with roman numbers. Asterisk denote pseudogenes and no. of genes in collapsed clades are indicated in brackets.