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. 2021 Mar 26;22:163. doi: 10.1186/s12859-021-04045-3

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© The Author(s) 2021

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 — Structural properties of CMH-I putative epitopes resembling segments from Tetanus toxin protein and chain A of the Measles hemagglutinin Protein. A Location of DISGINASVV on the structure of the six-helical bundle fusion core from the spike protein. B Calculation of SASA for the vaccines DISGFNSSVI and MSLSLLDLYL segment using a probe of 1.4 Å. C Crystal structure of the Measles virus hemagglutinin [22]. The peptide (in yellow) shows putative T-cell immunogenicity with the interaction pocket residues (light purple)