With regard to the segregation machinery, we identified a putative PrgP-PrgO partitioning system, upstream and inverted to the replicase gene.
Supporting the presence of a standard mRNA splicing machinery, we identified seven homologs of members of the spliceosome complex: Splicing factor 3B subunit 1, Splicing factor 3A subunit 3, splicing factor YT521, Splicing factor 1, splicing factor SLU7, Spliceosomal U5 snRNP-specific 15 kDa protein and Splicing factor U2AF 35 kDa subunit.
In trying to determine the type of siderophore produced and enzymatic machinery responsible, we identified isochorismatase (E.C 3.3.2.1; Table 4), an enzyme involved in the production of the siderophores vibriobactin, enterochelin and bacillibactin (KEGG pathway KO1053).
With a view to understand the functional role of ClpQY machinery in the parasite, we identified a peptide-based inhibitor that could be utilized to disrupt the interaction of PfClpQ and PfClpY, and hence inhibit function of ClpQY machinery in parasite.
In both the High and Low extracellular ATP groups, we identified components of machinery that regulate the trafficking of membrane proteins and associated vesicles through the endosome.
Furthermore, we identified the core RNAi protein machinery in Symbiodinium.
We propose that we identified a preferred relative rotation for SNARE-based fusion machineries between fusing membranes.
Among proteins containing this sequence we identified Atg9, another essential component of the autophagic machinery.
We identified NER proteins by MS suggesting physical association of Wss1 and NER machinery.
To uncover the JAM-A transduction machinery, we first sought to identify transcripts regulated by JAM-A expression.
