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. 2014 Apr 9;289(21):14458–14469. doi: 10.1074/jbc.M114.548156

TABLE 1.

LTQ-MALDI peptide mass fingerprinting of proteins differentially expressed in transgenic Arabidopsis expressing pBA002-AtPARK13 compared with plants expressing pBA002 alone with and without 37 °C heat treatment

Spot no. Protein Swiss-Prot Accession no. Mr pI Average -fold change
Function
21 °C 37 °C
Da -fold
Down-regulated proteins in pBA002-AtPARK13
    1 Photosystem II subunit P-1 Q42029 28,249 6.90 1.19 ± 0.08a 0.94 ± 0.21 Calcium ion binding, poly(U) RNA binding
    2 Peptidyl-prolyl cis-transp isomerase CYP20–3 P34791 28,532 8.83 1.08 ± 0.18 1.23 ± 0.09a Peptide binding, peptide-prolyl cis-trans isomerase activity
    3 Germin-like protein P92998 23,195 6.81 2.06 ± 0.84 1.824 ± 0.14a Manganese ion binding, Nutrient reservoir activity

Up-regulated protein in pBA002-AtPARK13
    4 Glutathione transferase O80852 24,148 7.03 1.35 ± 0.42 1.42 ± 0.01a Copper ion binding, glutathione binding, glutathione transferase activity, peroxidase activity

a Significantly (p < 0.05) different proteins at 21 and 37 °C as compared with transgenic plants harboring the empty vector controls.