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. 2019 Nov 4;9:15975. doi: 10.1038/s41598-019-52341-z

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© The Author(s) 2019

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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N-GlyDE prediction results of human VEGFR2, where sites with a prediction score above 0.6 (shown by the dotted line) are predicted as glycosites. Green bars represent the three glycosites with experimental evidence in UniProt. Glycosites annotated by sequence analysis in UniProt were recently validated by Chandler et al.’s mass spectrometry (MS) experiment on extracellular domain of murine VEGFR2, which shares 86% sequence similarity with human VEGFR2. Blue bars represent the MS-validated glycosites; the brown bar (N631) represents sites undetected in the MS experiment; and the orange bar (N66) represents the sequon only in human, not in murine. Red bars represent the non-glycosites, which was not studied by Chandler et al. The number following ‘N’ represents the asparagine position of the sequon in the sequence.