01. This is not surprising as values reasonably close to the cut-off point for significance would be expected to be very sensitive to changes in protein detection and sampling depth, with a small shift in the peptides involved in the calculations moving the protein over or under the significance cut-off point. A small number of proteins, 15, switched trend direction, moving from statistically significant increased

Vactosertib molecular weight or reduced abundance in internalized cells in the W83 analysis to the opposite trend in the ATCC 33277 analysis. The 15 proteins are listed in Table 2. In every case these 15 proteins showed inconsistency between two control cultures. In these cases the direction of change differed between the two controls with one control giving statistically significant

change in one direction and the other giving change in the other direction but without making the statistical cut-off. Again, we saw shifts in borderline cases, in these 15 instances enough to shift the direction of abundance change. We also found that some proteins detected using the W83 genome annotation were no longer detected using the ATCC 33277 annotation. In most cases this was due to the presence of a second similar protein in the ATCC 33277 annotation, but not in the W83 annotation. Peptides that could not be unambiguously assigned to a single protein were not retained for the finished dataset given in Additional file 1: Table S1. The presence of the same peptide sequence in another protein eliminated the data from consideration both here and in the original W83-based Smoothened Agonist clinical trial analysis. Despite the shifts in assigned click here q-values and abundance ratio magnitudes as a consequence of the change in annotations, the abundance trends observed for P. gingivalis virulence factors did not differ greatly from those reported previously [9], except as noted in Table 2. Table 2 The 15 proteins with opposite abundance trends. PGN0148 conserved domain protein PGN0152 Histidine ammonia-lyase immunoreactive 61 kDa antigen PG91 PGN0294 ragB lipoprotein RagB PGN0302 rubrerythrin PGN0503 mmdC methylmalonyl-CoA decarboxylase gamma subunit PGN0678 thiL thiamine monophosphate kinase PGN0914 peptidase M24 family PGN1032 hypothetical

protein PG_0914 PGN1403 acetylornithine aminotransferase putative PGN1529 oxidoreductase putative PGN1590 rplM ribosomal protein L13 PGN1830 TonB-dependent receptor putative PGN1849 rplO ribosomal protein L15 PGN1904 hemagglutinin protein HagB PGN2070 hypothetical protein PG_2204 Out of 1,113 detected (see Table 1) using both annotations, these 15 proteins showed inconsistent trends for significant (q ≤ 0.01) abundance change depending on whether the W83 [10] or ATCC 33277 [11] genome annotations were used for database searching. The ORF numbers and descriptors given are those for ATCC 33277. Metabolic pathways differentially regulated in internalized P. gingivalis The consensus assignments (see Additional file 1: Table S1) of differentially expressed proteins were used to populate metabolic pathways.