D polymer refine detection kit (Menarini/Leica, Germany). Tissue sections had been scanned at 230 nm resolution making use of a MiraxMidi Scanner (Zeiss MicroImaging GmbH, Germany) [48].Supporting InformationS1 Information. Excel spreadsheet Akt Modulators targets containing underlying numerical data and statistical analyses for Figs 1A, 5BE, 6B and 6C, 7B and 7C, 8AC, S1A, S7, S8B, S9A and S9B and S12A and S12B Figs. (XLSX) S1 Fig. PtdThr is often a key phospholipid in T. gondii. (A) HPLC profile of threonine obtained by hydrolysis of X1lipid from extracellular tachyzoites (107). Detection and quantification was accomplished by multiplereactionmonitoring (MRM) MS of threonine decarboxylation (transition, 120/74 Da). (B) Twodimensional TLC of lipids from tachyzoites (108) displaying major iodinestained phospholipids. Lipids had been identified by their migration patterns in comparison to genuine phospholipid requirements except for PtdThr, for which no industrial standard is available. (C) Chemical identity of PtdThr by MS evaluation. TLCresolved X1 band from panel B was confirmed as PtdThr by fragmentation pattern and m/z ratios. (TIFF) S2 Fig. Human foreskin fibroblast cells usually do not contain detectable amounts of phosphatidylthreonine. (A) Liquid chromatographymass spectrometry (LCMS) elution profile displaying the retention instances and peak intensities of phospholipids isolated from human fibroblasts. (B) MS evaluation with the indicated fraction revealing the prevalent occurrence of PtdSer species as well as a full lack of detectable PtdThr species. Fibroblast lipids had been detected within the damaging ionization mode, as described for the parasite lipids. (TIFF) S3 Fig. N-Methylbenzamide Description orthologs of PtdThr synthase are present in selected freeliving and parasitic protists but absent in most other organisms. Phylogenetic analysis from the orthologs of PTS and PSS from distinct organisms shows an early divergence of your two enzymes. TgPSS (ToxoDB: TGGT1_261480) clusters with the mainstream PSS clade that also comprises other parasite orthologs. In contrast, TgPTS (ToxoDB: TGGT1_273540) segregates with selected parasitic (Eimeria, Neospora, Phytophtora) and freeliving (Perkinsus) chromalveolates. Colored circles signify bootstrap values. Sequences for performing phylogenetic analysis (www.phylogeny.fr) had been obtained in the NCBI (www.ncbi.nlm.nih.gov) and parasite databases (www.ToxoDB. org). Accession numbers are indicated next for the sequence. NCBI accession IDs for TgPTS and TgPSS are KJ026547 and KJ026548, respectively. (TIFF) S4 Fig. PtdThr synthase from T. gondii harbors numerous substitutions in the catalytic domain of an otherwise universal baseexchangetype PtdSer synthase. (A) SecondaryPLOS Biology | DOI:ten.1371/journal.pbio.November 13,19 /Phosphatidylthreonine Is Needed for the Parasite Virulencestructure and membrane topology of TgPTS, as predicted by SOSUI plan (http://bp.nuap. nagoyau.ac.jp/sosui). (B) Amino acid sequence alignment of PSS and PTS from T. gondii with orthologs from indicated organisms. The diamond and arrow indicators specify the residues contributing towards the PSS activity and to substrate binding, respectively. Other conserved residues in PSS proteins show distinct substitutions in PTS orthologs (colored boxes). Gray bar below the alignment denotes the transmembrane domain. (TIFF) S5 Fig. Immunofluorescence costaining of TgPTSHA with organellespecific markers. Transgenic parasites ectopically expressing TgPTSHA beneath the manage from the TgGRA1 promoter and 3’UTR in the UPRT locus were generated by FUDR.