Analysis of phosphorylation sites on proteins from Saccharomyces cerevisiae by electron transfer dissociation (ETD) mass spectrometry -- Chi et al. 104 (7): 2193 Data Supplement - HTML Page - index.htslp -- Proceedings of the National Academy of Sciences

Chi et al. 10.1073/pnas.0607084104.

Supporting Information

Files in this Data Supplement:

SI Table 2
SI Table 3
SI Figure 6
SI Table 4
SI Table 5
SI Figure 7

SI Figure 6

Fig. 6. SCANSITE motif enrichment in phosphoproteins. Counts of each SCANSITE motif recovered in these phosphopeptides relative to those drawn from identically sized random genomic samples.

SI Figure 7

Fig. 7. Conservation of phosphorylation sites. Conservation of phosphorylation sites relative to identically sized random samples. SS and TT represent conserved serine and threonine sites, while ST and TS represent serines in yeast converted to threonines in another organism and vice versa. The five model organisms used were A. gossypii, C. elegans, D. melanogaster, H. sapiens, and A. thaliana. The fungal scan covered all genomes covered by BlastP through the Saccharomyces Genome Database (www.yeastgenome.org).