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. 2018 Oct 30;8:16053. doi: 10.1038/s41598-018-34415-6

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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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Structure of β-glucan synthases. (a) Structure of ScrFKS1 (on contig 5) and ScrFKS2 (on contig 4) genes in S. crispa. The intron-exon structure is shown above, while transcriptome mapping results are shown below. Transcriptional directions are shown by arrows. (b) Structure of ScrFKS1 and ScrFKS2 proteins. The transmembrane domains predicted by TMHMM are shadowed, and their clusters are marked with TM1 and TM2. The regions homologous to FKS1 domains (FKS1) and glucan synthases (GS) predicted by Pfam are shown in orange and green, respectively. The potential N-glycosylation sites predicted by ScanProsite are shown by open triangles, and the exon-intron junctions are shown by filled triangles.