(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 > Protostomia: NE > Ecdysozoa: NE > Panarthropoda: NE > Arthropoda: NE > Mandibulata: NE > Pancrustacea: NE > Hexapoda: NE > Insecta: NE > Dicondylia: NE > Pterygota: NE > Neoptera: NE > Paraneoptera: NE > Hemiptera: NE > Sternorrhyncha: NE > Aphidomorpha: NE > Aphidoidea: NE > Aphididae: NE > Aphidinae: NE > Aphidini: NE > Aphis [genus]: NE > Toxoptera: NE > Aphis citricidus: 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 MNQWLLWFGYLVASTYGLSLRHARHQSVGTPTAEEILEPQILIEDTDHVF RQRASDMFAQEPEYTEKRNLNHRRRSEFSGNQNTDFESSGKTYRTYRSDD PLIIHTNKGKIRGITQAATTGKLVDAWLGIPYAKKPLGDLRFRHPRPTDR WDTTSPETILDCTTPPNTCVQIFDTLFGDFPGATMWNPNSPVSEDCLYIN VVVPKPRPQNAAVMVWIFGGGFYSGSATLDIYDPKILVSEENVILVSMQY RVASLGFLYFDTEDVPGNAGLFDQLMALQWVHENIQLFGGNPNNVTLFGE SAGAVSVSLHLLSPLSRNLFNQAIMESGSSTAPWAILSREESFSRGLKLA KAMGCPNDRNEIHKTVECLRKVNSSEMVEKEWDHVAICFFPFVPVVDGAF LDDYPQKSLSTNNFKKTNILMGSNSEEGYYSIFYYLTELFKKEENVVVSR ENFIKAIGQLNPNADAAVKSAIEFEYTDWFSPNDPEKNRNALDKMVGDYQ FTCNVNEFAHKYALTGNNVYMYYFKHRSLNNPWPKWTGVMHGDEISYVFG DPLNPNKNYEIEEIELSKKMMRYWTNFAKTGNPSKTLEGSWVTPKWPVHT AYGKEFLTLDTNNTSIGVGPRLEQCAFWKNYVPDLTAISKSMKSDKNCTT ISGGTKTNMIELSVWTIVMTTAVLML
Reference
Title: Functional characterization of two acetylcholinesterase genes in the brown citrus aphid, Aphis (Toxoptera) citricidus (Kirkaldy), using heterologous expression and RNA interference Mou X, Yuan GR, Jiang HB, Liu Z, Wang JJ Ref: Pestic Biochem Physiol, 138:76, 2017 : PubMed
Acetylcholinesterase (AChE) is the primary target of organophosphate- and carbamate-based insecticides. We sequenced the full-length cDNAs of two AChE genes from the brown citrus aphid Aphis (Toxoptera) citricidus (Kirkaldy). These two genes, Tcace1 and Tcace2, which encode TcAChE1 and TcAChE2, respectively, had a shared amino acid identity of 29% and were highly similar to other insect ace1 and ace2 genes, respectively, having specific functional motifs. Potential differences in enzymatic function were characterized by the heterologous expression of the two genes using a baculovirus system in Sf9 insect cells. Both of the recombinant AChEs had high specific activities for three typical substrates, acetylthiocholine iodide, butyrylthiocholine iodide, and propinylthiocholine iodide. TcAChE1 had a lower Michaelis-Menten constant value and a higher maximal reaction velocity than recombinant TcAChE2, indicating a higher affinity for substrates and greater catalytic efficiency, respectively. Bioassays showed a greater sensitivity of recombinant TcAChE1 to the 10 tested insecticides. Silencing of Tcace1 and Tcace2 by RNA interference significantly increased the susceptibility of A. citricidus to malathion and carbaryl; however, silencing Tcace1 resulted in a higher mortality rate than silencing Tcace2. Additionally, the specific enzyme activity decreased more after silencing Tcace1 than after silencing Tcace2. Thus, TcAChE1 plays a major role in postsynaptic neurotransmission in A. citricidus.
