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. 2019 Aug 7;9:11440. doi: 10.1038/s41598-019-47725-0

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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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^{(a,b) The RMSF of C}α ^{atoms of all residues averaged over 9 protomers calculated from 40-} ns MD trajectories for the wild-type (black), E84A E85A mutant (red), and E84K E85K mutant (green) lysenin embedded in mixed lipids (a) and pure POPC lipids (b). (c–h) The number of lipids interacting with different residues of the PFM region (c,e,g) and the C-terminal domain (d,f,h), averaged over 40-ns MD trajectories are shown for different lipid types including CHOL (black), POPC (blue), POPE (green), POPI (red), and SM (orange).