Table 1.
Peptide | Δδ Gly10 Hα/Hα′ (ppm) | Fraction Folded (%) | ΔGfold (kcal mol−1) | ΔΔGfold vs. 1 (kcal mol−1) |
---|---|---|---|---|
1 | 0.20 | 65 | −0.3 | |
| ||||
2 | 0.26 | 83 | −0.9 | −0.6 |
| ||||
3 | 0.12 | 39 | +0.2 | +0.5 |
| ||||
4 | 37 b | +0.3 | +0.6 | |
4trans (60%) | 0.19 | 61 | −0.3 | +0.0 |
4cis (40%) | 0.09 | |||
| ||||
5 | 19b | +0.8 | +1.1 | |
5trans (76%) | 0.09 | 30 | +0.5 | +0.8 |
5cis (24%) | 0.00 | |||
| ||||
6 | 29b | +0.5 | +0.8 | |
6trans (65%) | 0.12 | 38 | +0.3 | +0.6 |
6cis (35%) | 0.00 | |||
| ||||
7 | 55b | −0.1 | +0.2 | |
7trans (87%) | 0.20 | 63 | −0.3 | +0.0 |
7cis (13%) | 0.12 |
NMR carried out at 5 °C in pH 6.3 phosphate buffer. Assuming a 0.01 ppm uncertainty in measured Gly Hα/Hα′ separation, error propagation estimates uncertainties of 5% for fraction folded and ~0.2 kcal mol−1 for ΔGfold and ΔΔGfold.
Overall folded population calculated as product of the fraction of peptide in the trans amide configuration and fraction folded for trans isomer.