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. 2018 Jan 29;9(3):198–203. doi: 10.1021/acsmedchemlett.7b00458

Table 1. Binding Constant, Free Energy, Enthalpy, and Entropy of Binding at 300 K Derived from ITC Measurements for M2TM WT (from Udorn, Upper Table) and the M2TM S31N (Lower Table).

liganda Kdb ΔGc ΔHd TΔSe
M2TM WT
1 2.17 ± 0.52 –7.77 ± 0.14 –6.66 ± 0.50 –1.11 ± 0.52
2 0.51 ± 0.26 –8.64 ± 0.30 –7.60 ± 0.28 –1.04 ± 0.41
2-R 0.32 ± 0.16 –8.97 ± 0.26 –7.54 ± 0.34 –1.42 ± 0.43
2-S 0.34 ± 0.12 –8.88 ± 0.21 –7.73 ± 0.28 –1.15 ± 0.35
3 0.13 ± 0.12 –9.30 ± 0.43 –4.19 ± 0.28 –5.12 ± 0.51
4 4.59 ± 2.21 –7.33 ± 0.28 –3.29 ± 0.62 –4.03 ± 0.68
5 3.43 ± 1.05 –7.50 ± 0.18 –6.23 ± 0.45 –1.27 ± 0.48
M2TM S31N
13 f f f f
5 >10 f f f
a

See Scheme 1.

b

Binding constant Kd in μM 2.

c

Free energy of binding in kcal mol–1.

d

Binding enthalpy in kcal mol–1.

e

Entropy of binding in kcal mol–1.

f

Values could not be determined reliably due to the limitations of the methods in the area of very weak binding (see also SI for definition of quantities).