It is of interest to note that motif C includes part of the original sequence isolated in the yeast two-hybrid assay; this sequence is underlined in Figure1. Figure2 shows the results obtained when the SsPAQR1 sequence was analyzed for transmembrane domains using the TMHMM server v. 2.0 and TOPO 2 [32]. This figure shows the 7 transmembrane domains that

characterize these receptors. According to the TMHMM server, SOSUI server and PSIPRED Protein structure prediction server (MEMSAT-SVM) analyses [32–34], the N-terminal domain is extracellular and the C-terminal domain is intracellular as shown. Danusertib PSORT II analysis identified the localization of this receptor in the plasma membrane with a 45% probability [35]. Signal peptide analysis using Predotar [36], TargetP [37] or MitoProt [35] showed that the SsPAQR1 has no mitochondrial

targeting signal peptide at its N-terminal as compared to PAQR 9, 10 and 11 that have mitochondrial localization signals. MEMSAT-SVM analysis identified a signal peptide comprising the region from amino acids 1 to 39 [34]. This signal sequence possibly allows its passage through the ER to its final destination. Figure 2 Transmembrane domain analysis of SsPAQR1. Figure2 Epacadostat shows the transmembrane domain analysis of SsPAQR1 obtained using TMHMM server v. 2.0 (http://www.cbs.dtu.dk/services/TMHMM) for the prediction of transmembrane helices. The 7 transmembrane domains that characterize Chloroambucil this receptor family are shown. Membrane topology was visualized with TOPO2 (http://www.sacs.ucsf.edu/TOPO2/). A multiple sequence alignment of the derived amino acid sequence of SsPAQR1 to other fungal homologues and the human PAQR7 is included in Additional file 1. BLAST search for

the predicted amino acid sequence identified this protein as 65 to 80% identical to other PAQRs of fungi such as: Neurospora crassa, Magnaporthea oryzae, Giberella zeae, among others. It is also shows that it is approximately 50% identical to S. cerevisiae Izh3 family channel protein. Co-immunoprecipitation (Co-IP) and western blots The SSG-2/SsPAQR1 interaction was corroborated using co-immunoprecipitation and Western Blot as shown in Figure3. Lane 1 shows the band obtained using anti-cMyc antibody that recognizes SSG-2. This band is of the expected size (58 kDa) considering that SSG-2 was expressed fused to the GAL-4 binding domain. Lane 2 shows the results obtained in the Western blot when the primary anti-cMyc antibody was not added (negative control). Lane 3 shows the band obtained using anti-HA antibody that recognizes the original SsPAQR1 fragment isolated from the yeast two-hybrid clone. This band is of the expected size (22.