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. 2012 Jan 16;441(Pt 3):803–812. doi: 10.1042/BJ20111474

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© 2012 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Modelling of the interaction between human PABP1 PABC (green) and the eRF3-N PAM2 motif (purple) when Lys⁶⁰⁶ is dimethylated (middle panel) or acetylated (bottom panel), based on the crystal structure of unmodified PABC [18] (top panel). Key residues are numbered according to their position in full-length PABP1 or the eRF3-N PAM2 motif (1–12). Depiction, labels and colour scheme are as in Figure 4.