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. 2008 Oct 22;105(43):16496–16501. doi: 10.1073/pnas.0802779105

Table 2.

Chemical structures and physicochemical properties of isoleucine, methionine, and methionine sulfoxide

graphic file with name zpq999085301t002.jpg
LogP 2.38 1.63 −0.50
p [D] 0.01 1.56 3.79
A [Å2] 117.7 122.0 125.0
Ap [Å2] 0.0 0.0 22.3

The following properties were calculated for the displayed amino acid side chains depicted in bold: LogP, octanol-water partition coefficient; p, dipole moment; A, Connolly molecular surface area; Ap, polar surface area. Transitions from isoleucine to methionine are accompanied by a loss in sterical demand in the β position, whereas the overall elongated and hydrophobic character of the side chain is largely maintained.