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. 2020 Aug 20;21:569. doi: 10.1186/s12864-020-06971-7

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 5 — Presence of homologs of gliding motility and type 9 secretion proteins in the predicted proteomes. Presence of homologs is indicated by light blue squares and absence by white squares. Strains sequenced in the framework of this study are indicated in bold. Each species was annotated based on its taxonomy (Groups) and motility as reported in literature. Protein names in bold are considered essential or important for F. johnsoniae gliding. The rest of the proteins are either non-essential or their role in F. johnsoniae gliding has not been determined [24, 32]. Other, gliding motility mechanism other than T9SS-based; NA, no information available (see also Additional file 3)