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. 2020 Oct 6;21:692. doi: 10.1186/s12864-020-07102-y

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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. 2 — a; Isoelectric point distribution of proteins within piezophilic (blue points) or piezosensitive (black) strains, with an average line of fit within each group. b; Isoelectric point protein bias within each strain as a function of their growth pressure. c; Asymmetry index values indicating preference of amino acids in the piezophiles or C. psychrerythraea 34H within orthologous proteins present in all strains. d; Specific amino acid substitutions from C. psychrerythraea 34H to the piezophiles within orthologous proteins. The substitutions shown were also identified within comparisons between piezophilic and piezosensitive Shewanella