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. Author manuscript; available in PMC: 2014 Jun 16.
Published in final edited form as: Angew Chem Int Ed Engl. 2013 Nov 19;52(52):13975–13979. doi: 10.1002/anie.201305882

Figure 1.

Figure 1

Molecular structures of the N-tL (A) and C-tL (B) developed against the C-terminal epitope of Akt2 near the pS474 residue. The 1° and 2° ligand branches are common to both PCC agents, and are drawn in red and blue, respectively. The poly (ethylene glycol)-linked biotin groups were included in the development process and thus do not represent interfering perturbations.