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. 2019 Mar 4;9:3331. doi: 10.1038/s41598-019-39219-w

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© The Author(s) 2019

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Antimicrobial activity of HR1-18 depends not on structure-defining parameters. Sensitivity of P. a. ATCC 10145 towards HR1-18, a retro-analog with the reversed AA-sequence of HR1-18 (reverse HR1-18), a peptide with a scrambled AA-sequence of HR1-18 (scrambled HR1-18) and an enantiomeric HR1-18 peptide where all L-amino acids have been replaced by D-amino acids ((D)HR1-18) were tested in 10 mM NaP/0.25% glucose/pH 5.5. AA-sequences are shown in Supplementary Table 5. Data are mean ± s.e.m. (n = 3).