(Below N is a link to NCBI taxonomic web page and E link to ESTHER at designed phylum.) > cellular organisms: NE > Eukaryota: NE > Opisthokonta: NE > Metazoa: NE > Eumetazoa: NE > Bilateria: NE > Platyhelminthes: NE > Trematoda: NE > Digenea: NE > Plagiorchiida: NE > Echinostomata: NE > Echinostomatoidea: NE > Fasciolidae: NE > Fasciola: NE > Fasciola hepatica: NE
LegendThis sequence has been compared to family alignement (MSA) red => minority aminoacid blue => majority aminoacid color intensity => conservation rate title => sequence position(MSA position)aminoacid rate Catalytic site Catalytic site in the MSA MIRSQQPTTSVEGEVDQISWEETVLGRSPSVSNLRVSECRRRFTSVCWLN LVLLFTLMIAIAVILYFVVQPYIQARNYQAQTVVNTLCGTLQGFVNSDGI ITFLGIPYALAPVGVNRFKRPVELTTQELCKQAWGTNSSDMVHLVTQYKS PCMQLEPITDKLVGNEDCLYANVFVPVSDQPLTPSTARPVIVQISGLFFL YGGSAAGLSVTAGQQPHARTVRTVDAIHVTFNHRIGPLGFLTHPRTKQPN LGLYDQLALLRWIRSNIGAFGGDPTRVTLFGYGSGATCALALSQSLLGHS LFDRLWISAPALGLPKLSLEEAVTHSEQLFECNSSLNASCEAGYLNDGPS ILRLWSWFHMEPWLKQGLFSLPDLTSDSMNLDKSTRSWFDRILVDDGNLV DARRWYNPTYTVPTVIGQTGHEAALYLAPVTVPFWDETFYQQYLLGRLAQ DESSKMDLITQLRFALTDPTCSNRSQPKQITDVEAHLTSLITDARYTCPL TQVVRKWTEQGQPIYRYYLISTHRRFDPYALSSFVSLAFHGWDGMLYLRG YLSHPDYISSGLVFSNEQEVDDLLQMSQLLNRAMHEFSRTGRIRQWKPSE SDWDHVNLIDEGQVCRPWKFLEQRCKVWEHLIGSPDLLHLAWPV
Bioinformatics analysis of the complete transcriptome of Fasciola hepatica, identified a total of ten putative carboxylesterase transcripts, including a 3146 bp mRNA transcript coding a 2205 bp open reading frame that translates into a protein of 735 amino acids, resulting in a predicted protein mass of 83.5 kDa and a putative carboxylesterase B enzyme. The gene coding for this enzyme was found in two reported F. hepatica complete genomes stretching 23,230 bp, containing two exons of 1282 and 1864 bp, respectively, as well as a 20,084 bp intron between the exons. The enzymatic activity was experimentally assayed on F. hepatica protein extracts by SDS-PAGE zymograms using synthetic chromogenic substrates, confirming both the theoretical molecular weight and carboxylesterase enzymatic activity. Further bioinformatics predicted that this enzyme is an integral component of the cellular membrane that should be active as a 167 kDa homodimer complex and polyacrylamide gel electrophoresis (PAGE) zymograms experiments confirmed the analysis. Additional bioinformatics analysis showed that DNA sequences that code for this particular enzyme are highly conserved in other parasitic trematodes, although they are labeled hypothetical proteins.
