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. 2020 Sep 25;21:664. doi: 10.1186/s12864-020-07052-5

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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. 4 — Distribution of CLec variable protein paralogs in cyanobacterial genomes. DGR-internal variable proteins and remote variable proteins are indicated by triangles and asterisks over corresponding representatives. The CLec paralogs of VPs and RVPs are also shown for each genome. The CLec domain found in all paralogs is indicated by either a red square (CLec only) or two grafted domains shown as adjacent rectangles (C-terminal CLec in red; N-terminal domains in various colors). For clarity, paralogs of the same domain architecture in Trichodesmium erythraeum IMS101 are indicated below the representative protein (e.g. × 2). Note: only a representative subset of DGR-containing genomes is shown (15 of 52 genomes)