Skip to main content
. Author manuscript; available in PMC: 2017 Feb 19.
Published in final edited form as: ACS Chem Biol. 2015 Dec 28;11(2):491–499. doi: 10.1021/acschembio.5b00893

Figure 2.

Figure 2

Natural and synthetic polyamines used in this study. The 1,3-diaminopropane moiety in each molecule is shown in bold blue, putrescine (1,4-diaminobutane) in red and cadaverine in green (1,5-diaminopentane). Carboxyspermidine accumulates only in the ΔCASDC mutant. Each of the methylated carbon positions (in purple) of the methylated spermidine analogues is displayed on the same molecule.