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. 2018 Jan 22;8:1326. doi: 10.1038/s41598-018-19640-3

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© The Author(s) 2018

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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TatE paralogs in Gram-positive bacteria. The degree of sequence similarity, indicated by the percent of identity and the expect e-value (which decreases with the lower chance of random match) between Tat proteins from Escherichia coli and Corynebacterium glutamicum (A) and Bacillus subtilis (B), respectively, were calculated using NCBI BLAST (upper panels). (A) The closest homologue of C. glutamicum TatE is TatA from E. coli, both featuring non-charged N-termini as revealed in the multiple sequence alignment (lower panel). (B) In B. subtilis, TatAc is most similar to TatE of E coli, as shown by the common ExxxxK motif. Sequence source: C. glutamicum TatA (Q8NQE4), TatE (Q2MGW8), TatB (Q8NRD0); B. subtilis TatAy (O05522), TatAc (O31804), TatAd (O31467).