APETx1 structure (PDB ID: 1WQK) was used as a template by I-TASSER software for the molecular modeling of the toxins. The estimated accuracy of the models were evaluated by I-TASSER software, and were validated by the tools Anolea, DFire, QMEAN, Gromos, Endocrinology antagonist Promotif and ProCheck, available in the “structure assessment” tool of the SWISS-MODEL structure homology-modeling server (http://swissmodel.expasy.org/workspace/) [3], [4], [5], [40], [42], [56] and [88]. All the graphic designs represented

were rendered by PovRay (version 3.6 by Persistence of Vision Raytracer, Pty., Ltd.). The reversed-phase chromatographic fractions were assayed on male shore crabs Uca thayeri weighing 2–4 g, based on the well know crab bioassay used for detection of sea anemone neurotoxins [7] and [76]. Samples were injected (10 μL/g crab weight) into the base of the

third walking leg. A dose of 2 μg/g crab weight (2000 μg/kg) was assayed for toxicity screening and 6 crabs were used per sample. The toxicity was considered positive when the crabs placed upward were unable to right themselves within two hours after toxin administration. Furthermore, symptoms evoked by toxin administration were carefully observed. The immersion of S. helianthus in distilled water yielded 178 mg (average: 89 mg/specimen) whereas B. granulifera specimens yielded 203 mg of total proteinaceous content (average: 20.3 mg/specimen). Both exudates were submitted to gel filtration chromatography in Sephadex G-50 ( Fig. 1A and B). The chromatographic profile of B. granulifera exudate comprised Rapamycin clinical trial 6 main fractions ( Fig. 1B) and it was very similar to the Sephadex G-50 profile of B. cangicum, despite these exudates were obtained from different sea anemones

by using different extraction protocols. The neurotoxic fractions of S. helianthus and B. granulifera were named as Sh-3-4 and Bg-3-4, respectively. The neurotoxic fraction of S. helianthus (Sh-3-4) yielded 15 mg of peptide content (8.4% of the total proteinaceous content), and B. granulifera (Bg-3-4) 30 mg (14.8%). The reversed-phase and mass spectrometry data allowed the construction Mannose-binding protein-associated serine protease of peptide fingerprints of S. helianthus and B. granulifera, in terms of hydrophobicity and molecular mass. Additionally, the data obtained from a previous similar study of B. cangicum [85] was used for comparison with the sea anemones species involved in the present study. Aiming to facilitate the comparison among reversed-phase fractions, those were named similarly to the previous work [85]. Thus in the present study, the reversed-phase fractions were named as Sh or Bg (abbreviation of S. helianthus and B. granulifera) followed by a number representing the retention time (shown in Table 1). For example, Bg 6.11 is the RPC18 fraction from B. granulifera, eluted at 6.11 min. The neurotoxic fractions (Sh-3-4 and Bg-3-4) were submitted to reversed-phase-C18 high performance liquid chromatography. Thirty six fractions were collected from the S.