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. Author manuscript; available in PMC: 2016 Dec 22.
Published in final edited form as: Methods Enzymol. 2016 Feb 23;573:261–278. doi: 10.1016/bs.mie.2016.01.020

Fig. 2.

Fig. 2

Mechanism of LSD1 inactivation by cyclopropylamine analogs. Cyclopropylamine analogs form covalent bonds with the flavin cofactor of LSD1 through ring opening. The C4a and N5 atoms (top right and bottom right) serve as proposed points of attachment that occur after cyclopropyl ring opening (center).