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. 2017 Dec 21;8:2236. doi: 10.1038/s41467-017-02341-2

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© The Author(s) 2017

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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Fig. 5 — CPH1 is a central hub interacting with multiple proteins at the conoid. a Replicate mass spectrometry data sets generated with BirA fusion lines were analyzed using SFINX (http://sfinx.ugent.be/) to generate a proximity-based protein interaction network. Interactors of CPH1 and MyoH completely overlapped, and were partially shared with those for RNG2. Baits (BirA fusions)—deep blue nodes; prey (interactors)—light blue nodes. See Supplementary Data 2. b Localizations for the CPH1-MyoH-RNG2 interactome were analyzed for annotated and hypothetical proteins identified in the CPH1-MyoH-RNG2 interactome. Pie chart shows percentages of each category. The number in each category indicates protein number. N = 24 interactors. c Domains were analyzed for apical proteins and microtubule in the CPH1-MyoH-RNG2 interactome with InterPro. N = 17 interactors. b, c Protein localizations and domains for proteins in the CPH1-MyoH-RNG2 interactome were determined as defined in Supplementary Data 2. See also Supplementary Data 4, 5 and Supplementary Fig. 5 for GO term analysis. CC coiled coil, DCX double cortin microtubule-binding domain, myosin myosin A and H, prichextensin proline-rich motif present in plant cell wall, IDRs intrinsically disordered regions