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. 2022 Sep 28;45(6):1311–1328. doi: 10.1007/s13402-022-00719-z

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© The Author(s) 2022

Open AccessThis 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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Fig. 3 — Differentially abundant phosphosites of WPMY-1 proteins in co-culture with PC3 versus in mono-culture. A, Volcano plot showing differentially abundant phosphosites of ‘light’ WPMY-1 proteins in co-culture versus mono-culture. Increased phosphosites with a FC > 2.5 are represented by yellow dots; and FC > 5 phosphosites are represented by red dots. Phosphosites that decreased in abundance upon co-culture with PC3 by FC > 2.5 and FC > 5 are represented by light and deep blue dots, respectively. B, Cell signalling pathway enrichment of up-regulated WPMY-1 phosphoproteome in co-culture. Data from NCI-nature pathway database. C and D, Networks of proteins with increased (C) and decreased (D) phosphorylation abundance in WPMY-1 cells. Analysis was undertaken using STRING/Cytoscape