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. 2017 Mar 2;65(5):932–940.e6. doi: 10.1016/j.molcel.2017.01.003

Figure 3.

Figure 3

Additional Targets of Serine ADPr

(A) High-resolution ETD fragmentation spectrum of an HMGB1 peptide with ADP-ribose on serine 181 is shown.

(B) Schematic representations of HMGB1 (upper) and HMGA1 (lower). The three novel serine ADPr sites were identified in vivo. A box and B box, positively charged homologous DNA-binding structures; acidic tail, negatively charged region composed of 30 glutamic and aspartic acids, exclusively; AT, AT-hook with the Arg-Gly-Arg-Pro (RGRP) core motif.

(C) Serine ADPr sites identified in histone-depleted fractions. ADPr sites were identified using ETD mass spectrometry. Modified serines are in red.

(D) High-resolution ETD fragmentation spectrum of a PARP-1 peptide with ADP-ribose on serine 499, obtained by reprocessing a published dataset (Phanstiel et al., 2011). The chemical structure of ADP-ribose is depicted.

See also Figure S3.