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. 2020 Feb 5;18(8):1810–1829. doi: 10.1111/pbi.13343

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© 2020 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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Homology modelling of the GmSNAP18, GmSHMT08 and GmPR08‐Bet VI from Forrest (Peking‐type resistance). (a) The tetrameric GmSHMT08 with important residues highlighted. (b) One SHMT subunit with highlighted catalytic and structural residues labelled. (c) The predicted interaction between GmSHMT08 (left) and GmSNAP18 (right). Locations of the four TPR motifs (TPR1: yellow, TPR2: orange, TPR3: blue, TPR4: red) and polymorphisms (green) at the GmSNAP18 are shown (right). (d) The predicted interaction between the GmSNAP18, GmSHMT08 and GmPR08‐Bet VI protein complex.