4 [82] and TatP 1.0 [83] servers. Although these servers are designed for the same purpose (i.e. identify proteins secreted by the TAT system), the algorithms used for each differ and as such proteins identified as TAT substrates do not overlap 100% between the two prediction algorithms. Six ORFs were predicted

to be TAT substrates in strain ATCC43617, only one of which was identified by both algorithms (Figure 8). The TatP 1.0 server identified MCORF 312 and MCORF 1197 as proteins potentially secreted by the TAT system, but no twin-arginine motif was found within the signal sequences of these gene DNA Damage inhibitor products. Conversely, the TatFind 1.4 server identified MCORF 1917 as a TAT substrate and a twin-arginine

motif was observed Saracatinib in vivo between residues 18 and 23. Although the encoded protein does not specify characteristics of a prokaryotic signal sequence (i.e. n-, h-, c-region), a potential lipoprotein signal sequence cleavage site was identified using the LipoP server. Interestingly, the MCORF 1197 and MCORF 1199 gene products resemble cytochrome c molecules involved in the electron transport chain. Cytochromes have been predicted, as well as demonstrated, to be TAT substrates in several bacterial species [84–87]. MCORF 1917 exhibits similarities to iron-dependent peroxidases, which is consistent with the previously reported Non-specific serine/threonine protein kinase role of the TAT system in the secretion of enzymes that bind metal ions, while MCORF 518 resembles the phosphate ABC transporter inner membrane protein PstA [88]. MCORF 838 shows similarities to a family of C-terminal processing peptidases and contains important functional domains including a post-translational processing, maturation and degradation region (PDZ-CTP),

and a periplasmic protease Prc domain described as important for cell envelope biogenesis. Figure 8 Comparison of the putative TAT substrates identified in the genomes of M. GSK3326595 catarrhalis strains ATCC43617 a and BBH18 b . Six putative TAT substrates were identified in the genome of M. catarrhalis strain BBH18, five of which overlapping those predicted in ATCC43617 (Figure 8). Strain BBH18 specifies the unique TAT substrate MCR_920, which is predicted to be a highly-conserved phosphatase (Figure 8). The MCORF 1659 of strain ATCC43617 encodes a gene product that is 96.8% identical to this putative phosphatase, but neither of the TatFind 1.4 and TatP 1.0 servers identified the ORF as a TAT substrate, likely due to significant amino acid divergence in the signal sequence (data not shown). Strain BBH18 specifies a putative C-terminal processing peptidase (MCR_1063) that is 98.1% identical to the putative TAT substrate MCORF 838 of ATCC43617. Like the MCORF 838 of ATCC43617, the BBH18 gene product lacked a TAT motif in its signal sequence (data not shown).