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. 2015 Feb 27;427(4):737–752. doi: 10.1016/j.jmb.2014.11.021

Fig. 9.

Fig. 9

Comparison of the 13C-methyl-TROSY NMR spectra of wild type (a and c) and RAIDD-DD (E188K) (b and d) in the absence and presence of excess PIDD-DD. The positions of the cross-peaks of unbound RAIDD-DD (E188K) are essentially identical with those of the wild type. However, notable differences in the cross-peak clusters corresponding to the well-resolved RAIDD-DD Val189-Cγ2H3 cross-peak (highlighted by red rectangles) are detected, presumably reflecting both the proximity to the mutation site at residue 188 and the different overall stoichiometry of the complex formed.