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. 2022 Sep 7;11:e73031. doi: 10.7554/eLife.73031

Appendix 1—table 2. Protein are specified by the Uniprot identifier (Bairoch et al., 2005) and the corresponding gene ID.

For ions and chemical compounds, the ChEBI (Chemical Entities of Biological Interest Degtyarenko et al., 2008) identifier is used instead. The initial concentrations of all un-phosphorylated species and complexes between proteins were set to 0 pM.

Species Uniprot ID / Gene ID Initial Source
ChEBI ID Concentration
BRI1 O22476 At4g39400 0.182 633pM Wilma van Esse et al., 2011
BAK1 Q94F62 At4g33430 0.099 632pM Wilma van Esse et al., 2011
BIR3 0.237 423 11pM this study
AHA* 0.232 442pM [AHA1]+[AHA2]
AHA1 P20649 At2g18960 0.116 221pM assumption:AHA1AHA211
mRNA data (eFP Browser)
Winter et al., 2007
AHA2 P19456 At4g30190 0.116 221pM this study
AHA CT* C-terminus 0.232 442pM assumed to be
of AHAs [AHA1]+[AHA2]
BKI1 Q9FMZ0 At5g42750 0.219 16pM assumption:1.2[BRI1]t=0
BIK1 O48814 At2g39660 0.219 16pM assumption:1.2[BRI1]t=0
CNGC10 Q9LNJ0 At1g01340 0.1pM
H+in 24636 - 63 000pM
H+out 24636 - fitted to data
K+out 29103 - 9.8425 × 109 pM ½ MS medium
K+in 29103 - 8.4 × 1010 pM Maathuis and Sanders, 1993
K+vac 29103 - 8.4 × 1010 pM assumed to be identical to K+in
BL 28277 - dose see experimental setup
*

To avoid overly complicating the model we have summarized the pump activity of AHA1 and AHA2 into one reaction that is mediated by AHA, which is defined as the sum of [AHA1] and [AHA2]. Similarly, regulatory function of the C-terminal regions of the AHAs is mediated by the unphosphorylated form of the C-terminus AHA CT, which represents the C-terminal regions of both AHA1 and AHA2.