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. Author manuscript; available in PMC: 2018 Sep 15.
Published in final edited form as: ACS Chem Biol. 2017 Aug 30;12(9):2281–2286. doi: 10.1021/acschembio.7b00330

Figure 1.

Figure 1

The canonical HDAC substrate peptidyl acetyl-L-lysine and structurally-related cyclic tetrapeptide inhibitors. The ketone carbonyl group of each inhibitor is isosteric with the scissile carbonyl of acetyl-L-lysine.