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. 2013 Mar 15;288(18):13110–13123. doi: 10.1074/jbc.M112.444554

FIGURE 6.

FIGURE 6.

E7Ep peptide proline chemical shift assignment. A, selected region of the 1H-13C HMQC spectrum showing the chemical shift assignment of CH2 groups of positions β (left) and γ (right) of prolines at 20 °C. For both Pro-41 (P41) and Pro-47 (P47), the trans isomer is much more abundant at equilibrium (85 and 95%, respectively). B, selected region of the NOESY spectrum at 20 °C showing the cis and trans chemical shift assignments. Characteristic Hδ-Hαi − 1 NOEs are observed for the trans prolines, whereas Hα-Hαi − 1 cross-peaks are detected in the cis isomers.