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. 2022 Apr 20;298(6):101963. doi: 10.1016/j.jbc.2022.101963

Table 2.

Thermodynamic analysis of interactions

Syringe/cell Temperature (°C) Kd (nM) N ΔH (kJ mol−1) −TΔS (kJ mol−1) ΔG (kJ mol−1)
AtTAF4–RST/DREB2A 25 740 ± 320 1.24 ± 0.04 −5.19 ± 0.03 −29.8 −35.0
AtTAF4–RST/DREB2A 30 1050 ± 140 1.18 ± 0.01 −10.5 ± 0.2 −24.2 −34.7
AtRCD1–RST/DREB2Aa 25 16 ± 1 0.90 ± 0.00 −63.3 ± 0.2 18.7 −44.6
HsTAF4–TAFH/DREB2A 25 110 ± 50 1.15 ± 0.02 −15.4 ± 0.4 −24.1 −39.5
HsTAF4–TAFH/DREB2A 30 420 ± 120 0.85 ± 0.02 −23.9 ± 0.7 −12.9 –36.9
AtTAF4–RST/ANAC013 25 NB NB NB NB NB
AtTAF4–RST/ANAC013 30 1080 ± 630 0.68 ± 0.04 −1.8 ± 0.1 −32.7 −34.5
AtRCD1–RST/ANAC013b 25 9 ± 4 0.80 ± 0.01 −45.0 ± 0.8 −0.6 −45.6

Abbreviation: NB, no detectable binding.

Syringe/cell indicates whether the αα-hub domain or the TF is the titrant in the syringe or the titrant in the cell. The standard errors for ΔH, Kd, and N were obtained from Origin when fitting the data to a model of one set of binding sites.

a

Data from Ref. (28).

b

Data from Ref. (27).