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. 2024 Feb 26;52(6):3180–3198. doi: 10.1093/nar/gkae129

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© The Author(s) 2024. 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 11. — Tyrosine recombinases in Acinetobacter baumannii genomes. An iterative search was performed against all annotated proteins (67 128 995) of Acinetobacter baumannii genomes (17 469). The representative hits (232) were aligned with the MUSCLE algorithm. Aligned sequences were then used to build an approximately-maximum-likelihood phylogeny using the FastTree algorithm and displayed with iTOL(v6). Branch nodes with host XerC (light blue highlight) and XerD (light green highlight) are included with the major group of well-studied tyrosine recombinases from mobile genetic elements (magenta branches). Others branches of tyrosine recombinases are represented as black.