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. 2016 Nov 23;292(2):512–527. doi: 10.1074/jbc.M116.753426

TABLE 2.

Thermodynamic analysis by ITC of interactions between RCD1-RST(499–572) and different transcription factors

All experiments were performed as described under “Experimental Procedures.” Syringe/cell indicates whether RCD1-RST or the transcription factor is the titrant in syringe or the titrant in cell. The standard errors for ΔH, Kd, and N were obtained from Origin when fitting the data to a one set of sites binding model.

Protein Kd N ΔH TΔS ΔG Syringe/cell
nm kJ/mol kJ/mol kJ/mol
ANAC016(325–367) 200 ± 76 1.02 ± 0.04 −42.5 ± 2.3 4.2 −38.3 ANAC016/RCD1
ANAC017(296–339) 37 ± 9 0.89 ± 0.02 −54.2 ± 1.0 11.7 −42.5 ANAC017/RCD1
bZIP23(15–36) 128 ± 40 0.94 ± 0.05 −30.6 ± 2.1 −8.7 −39.3 RCD1/bZIP23
STO(229–248) 90 ± 90 1.16 ± 0.12 −3.8 ± 0.5 −36.3 −40.1 RCD1/STO
COL10(175–208) 418 ± 201 1.04 ± 0.08 −9.2 ± 1.0 −27.2 −36.4 RCD1/COL
bHLH19(271–295) NBa RCD1/bHLH19
IRL3(69–100) NB RCD1/IRL3
MYB91(100–291) NB RCD1/MYB91
MYB(100–230) NB RCD1/MYB91
MYB92(239–267) NB RCD1/MYB91
MYB91(239–291) NB RCD1/MYB91

a NB means no detectable binding.