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. Author manuscript; available in PMC: 2019 Feb 6.
Published in final edited form as: Biochemistry. 2018 Jan 10;57(5):631–644. doi: 10.1021/acs.biochem.7b01155

Figure 6.

Figure 6.

Population plot obtained with the scheme of Figure 5. The apparent pK of the alkaline transition is 9.26 and the fraction of protein with a distal lysine ligand (HK|H) is 0.55 at pH 10.5. The value of pK3 is then 9.64. K1/K2 is 1.38, corresponding to a free energy difference of 0.8 kJ mol−1 favoring the lysine bound form.