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Resolution: standard / high Figure 6.
A TGF-β receptor type I from Opisthorchis viverrini. Multiple sequence alignment of the ORFs of OvAE22 with homologues from Schistosoma mansoni (SmRK-I – GenBank AF031557), the hydatid tapeworm Echinococcus multilocularis (TR1 – AJ841786) and human (TGF-β receptor type I – L11695) (A). The overlined region denotes the putative serine-threonine kinase active site in
SmRK-I [44]. Residues highlighted in red font in OvAE22 are putative sites of serine/threonine
phosphorylation. Both SmRK-I and human TGF-β receptor type I sequences shown here
are truncated at the N-terminus and SmRK-I is truncated at the C-terminus for comparative
purposes with the partial sequence from O. viverrini. Black boxes denote identical residues shared by two or more of the sequences. Grey
boxes denote conservative substitutions. Neighbour joining phylogenetic tree showing
the relationship between the ORF of OvAE22 and other members of the TGF-β receptor
type I family (B). Numbers on branches denote bootstrap values from 100 samplings. The nominated outgroup
was the type 2 receptor, SmRK-2. GenBank accession numbers not already provided above
are as follows: pig bone morphogenic protein (BMP) receptor type I (AY065994); dog hookworm Ancylostoma caninum S/T kinase (AY053388); Caenorhabditis briggsae CBG02627 (CAAC01000012); filarial nematode Brugia pahangi trk-1 (AF013991); S. mansoni SmRK-2 (AY550912).
Laha et al. BMC Genomics 2007 8:189 doi:10.1186/1471-2164-8-189 |