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. 2004 Aug;24(16):7249–7259. doi: 10.1128/MCB.24.16.7249-7259.2004

TABLE 2.

Mass spectrometry analysis of SAGA purified from wild-type and sgf11 deletion strainsa

ORF Protein WT avg NPAF sgf11Δ avg NPAF NPAF sgf11Δ/WT ratio
YGR252W TRA1 0.00624 0.00475 0.7613
YDR145W SPT7 0.00661 0.00621 0.94
YLR055C TAF5 0.00649 0.00749 1.1529
YOL148C ADA3 0.01354 0.01425 1.0523
YDR448W SGF73 0.00774 0.00961 1.2419
YGL066W SPT20 0.00599 0.00817 1.363
YCL010C SPT8 0.00634 0.00905 1.4278
YBR198C TAF12 0.0054 0.00935 1.7327
YGL112C TAF6 0.00607 0.00626 1.0307
YDR176W ADA1 0.00711 0.00467 0.6565
YDR392W UBP8 0.00686 0 0
YBR081C GCN5 0.00405 0.00875 2.1584
YMR236W ADA2 0.01256 0.01597 1.2718
YHR099W SPT3 0.00738 0.007 0.9477
YPL254W SGF29 0.01307 0.01538 1.1766
YDR167W TAF10 0.00545 0.00343 0.6288
YMR223W TAF9 0.00708 0.00587 0.8289
YPL047W SGF11 0.00458 0 0
a

Proteins immunoaffinity purified with Gcn5p from the wild type (WT) and from a sgf11Δ deletion strain were identified by DALPC mass spectrometry. To estimate the relative composition of individual components in purified SAGA, the PAF value for each subunit was normalized to the total number of nonredundant spectra identifying the entire SAGA complex (see Materials and Methods). We call this value the normalized PAF (NPAF). The table shows the average NPAF values from duplicate experiments and the ratio of these averages from the two strains. The overall average ratio ± its SD was 1.02 ± 0.527.