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. 2021 Apr 2;11:7466. doi: 10.1038/s41598-021-86820-z

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© The Author(s) 2021

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 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/.

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Alignment of the amino acids of nuclear RPL32 of Euphorbia schimperi, Populus alba (BAF80584.1), Passiflora biflora; (QKY65178.1), P. contracta; (QKY65180.1), P. oerstedii; (QKY65177.1) and P. pittieri; (QKY65179.1) and Populus alba nuclear SOD-1(BAF80585.1). Pink annotation indicates plastid transit peptide of SOD-1 in Populus. Purple annotation indicates a conserved domain of RPL32 in Populus. Open and filled triangles indicate the position of introns in the cp rpl32 and cp sod-1 genes in Populus (Ueda et al. 2007). Pairwise aa sequence identity of nuclear-encoded RPL32 from E. schimperi, Populus alba, Passiflora (P. biflora, P. contracta, P. oerstedii and P. pittieri) and nuclear-encoded SOD-1 of Populus alba was 59.4% and 88.9% for transit peptide and the ribosomal protein L32 conserved domain, respectively. Gaps are indicated by dashes.