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. 2022 Oct 27;50(19):11285–11300. doi: 10.1093/nar/gkac934

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© The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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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Figure 1. — Sequence alignments of HflX and HflXr proteins and MIC data. (A) Sequence alignment of the resistance-associated loop region within the N-terminal domain of selected HflX (blue) and HflXr (pink) representatives, showing independently evolved insertions in HflXr and HflX. Taxa in bold are those with both HflX and HflXr. Conserved R/Q residue (R149 in L. monocytogenes HflXr) is marked with a red asterisk. The full alignment is found in Supplementary Data S1. (B) Minimum inhibitory concentrations (MICs) of ribosome-targeting antibiotics against L. monocytogenes EGDe strains lacking or expressing HflXr or/and VgaL/Lmo0919 ARE-ABCF. The color code is made with respect to the first column that contains the ΔvgaL/pIMK3 MICs.