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. 2017 Jun 7;7:3013. doi: 10.1038/s41598-017-03369-6

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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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Properties of the lysine crotonylation sites. (a) Sequence probability logos of significantly enriched crotonylation site motifs around the lysine crotonylation sites. (b) Heat map of the amino acid compositions around the lysine crotonylation sites showing the frequency of different types of amino acids around this residue. Red indicates enrichment and green indicates depletion. (c) Probabilities of lysine crotonylation in different protein secondary structures (alpha helix, beta-strand and disordered coil). (d) Predicted surface accessibility of crotonylation sites.