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. 2018 Mar 20;8:85. doi: 10.3389/fcimb.2018.00085

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Copyright © 2018 Ni, Fan, Li, Wu, Hou, Hu, Zheng, Zhu, Wang, Cao, Shao and Pan.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Identification of DivIVA phosphorylated sites. (A) Protein sequence of DivIVA: The peptide containing a phosphorylated signal is highlighted in yellow and labeled with arrows. The threonine residues introduced by mutagenesis are labeled in green. (B) Mass spectra showing that DivIVA is phosphorylated at threonine 199. Recombinant DivIVA was incubated with rSTK and then subjected to trypsin digestion. (C) rSTK incubated with mutant DivIVA proteins were separated by SDS-PAGE and then stained with Coomassie blue. (D) An anti-pThr antibody was used to assess the effect of mutant DivIVA proteins.