Skip to main content
. Author manuscript; available in PMC: 2017 Sep 8.
Published in final edited form as: Methods Enzymol. 2016 Jun 24;580:303–332. doi: 10.1016/bs.mie.2016.05.035

Table 2.

Primary Sequences of Model Peptides

Peptide Sequence Calculated m/z Observed m/z
1 CPWRATNPFC 1235.45 1234.91
2 pa-VCNATCHIWH 1262.47 1262.42
3  VCNATCHIWH 1224.43 1224.57
4  VCNATHCIWH 1224.43 1223.26
5  VCNATIHCWH 1224.43 1223.26
6  VCNATSHIWH 1208.36 1208.54
7  VCNATMHIWH 1252.48 1252.59
8  VMNATMHIWH 1280.53 1280.73

All peptides were prepared with C-terminal amides and N-terminal acetyl groups, except for peptide 2 which was prepared with an N-terminal pentynyl group (denoted pa-) as shown in Fig. 5. Sulfur-containing amino acids capable of participating in macrocyclization reactions are shown in bold. Observed m/z are reported as major peaks from MALDI mass spectra.