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. 2021 Apr 21;203(10):e00631-20. doi: 10.1128/JB.00631-20

TABLE 1.

MaxQuant iBAQ quantitation of proteins coimmunoprecipitated with anti-A-LPS from a mix of 33277 wzy and 381 porU strainsa

Protein name Locus tagd LFQ intensity
LFQ ratio iBAQ abundance No. of peptides (mix)
Mix Negative
RgpBb PGN_1466 7.6E+08 1.27E+08 6.0 2.5E+07 9
HBP35 PGN_0659 2.5E+08 2.4E+06 106.4 1.4E+07 7
RgpAc PGN_1970 7.8E+08 1.4E+08 5.4 1.2E+07 11
RgpB PGN_1466 7.8E+08 1.4E+08 5.4 1.2E+07
PPAD PGN_0898 8.0E+07 0 2.7E+06 10
Unknown function PGN_1321 1.3E+07 0 6.3E+05 3
Unknown function PGN_1366 2.5E+07 9.6E+05 26.3 6.2E+05 6
47-kDa antigen PGN_0852 7.8E+06 0 4.1E+05 4
Transketolase PGN_1689 5.5E+06 0 2.1E+05 2
CPG70 PGN_0335 4.2E+06 0 1.2E+05 2
Ribonuclease E/G PGN_1391 4.0E+06 0 8.3E+04 3
AcrB-type transporter PGN_1430 5.2E+06 0 7.6E+04 2
a

T9SS cargo proteins are shaded.

b

RgpB is inferred considering that peptides in common between RgpA and RgpB were enriched in the mix, whereas the RgpA-specific peptides were depleted (see Materials and Methods and Fig. 5). These data were therefore produced by removing the RgpA sequence from the database.

c

Because the sequences of RgpA and RgpB catalytic domains are very similar, the data generated using both sequences in the database could not distinguish between the two proteins.

d

The locus tag can be found in the National Center for Biotechnology Information database (NCBI), https://www.ncbi.nlm.nih.gov.