Figure 3.
Fig. 3. Comparison of the and aspartyl
isomers of MCoTI-II. a, structure of and aspartic
acid residues and sequential NOEs expected to be observed in the
-Asp form.
b, comparison of the -proton
chemical shifts of the two isomers of MCoTI-II. The fact that
the differences occur only near residue Asp-5 suggests that
isomerization of this residue ( / aspartic
acid) is responsible for the differences between the two
isolated peptides.
The above figure is reprinted
by permission from the ASBMB:
J Biol Chem
(2001,
276,
22875-22882)
copyright 2001.
and 
aspartyl
isomers of MCoTI-II. a, structure of