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. Author manuscript; available in PMC: 2007 May 2.
Published in final edited form as: Peptides. 2006 Nov 30;28(1):109–118. doi: 10.1016/j.peptides.2006.09.019

Figure 1.

Figure 1

Figure 1

ClustalW alignment of the deduced amino acid sequences of the Open Reading Frames (ORFs) of dipteran sNPFs and sNPFRs. (A) Alignment of the deduced sNPF prepropeptides of An. gambiae (GenBank DQ437578) and Ae. aegypti (GenBank DQ459411). The predicted signal peptides are underlined, processed form of sNPFs are in bold, convertase cleavage sites are boxed and C-terminal amide donors are shaded. Locations of introns are denoted by a ▾placed above the amino acid sequences. For the D. melanogaster prepropeptide (CG13968-RA), see [24]. (B) Alignment of the deduced sNPFR ORFs of An. gambiae (Ang; GenBank DQ437579), Ae. aegypti (Aea; ENSEMBL Supercontigs 1.289 and 1.858) and D. melanogaster (Drm; CG7395). The predicted transmembrane domains (TM) are underlined, and intracellular (ICL) and extracellular (ECL) loops labeled. For Ang-SNPFR, predicted start methionines are in bold shaded, signal peptide is double underlined, potential N-glycosylation sites are shaded and phosphorylation sites in bold.