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. 2018 May 24;19:393. doi: 10.1186/s12864-018-4715-9

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — Comparison of the sequences of the diagnostic domains of Par6: The N-terminal Phox and Bem1 (PB1) domains required for interaction with the PB1 domain of atypical Protein Kinase C (aPKC); the semi-CRIB (Cdc42/Rac interactive binding) domain and the C-terminal Postsynaptic-density-95/Disc-large/Zona-occludens1 (PDZ) domain required for the interaction with Par3. Sequences were aligned with MAFFT v.7 and visualized with Jalview 2.9. Critical residues are labelled in red: Lysine K19 in PB1 domain is essential for the interaction with aPKC; Proline 136 (P136) in the semi-CRIB motif is necessary to bind cdc42; Methionine 235 (M235) in the PDZ domain binds the LGL protein