Difference between revisions of "Team:NCTU Formosa/Model"

Line 245: Line 245:
 
     <!--1.-->
 
     <!--1.-->
 
     <div class="modelingPart">
 
     <div class="modelingPart">
         <h2 class="content-1" id="titleA" style="color#EBEB00">I. Purpose</h2>
+
         <h2 class="content-1" id="titleA" style="color:#EBEB00">I. Purpose</h2>
 
         <div class="modelingPartContent" id="partA">
 
         <div class="modelingPartContent" id="partA">
  
Line 290: Line 290:
  
 
     <div class="modelingPart">
 
     <div class="modelingPart">
         <h2 class="content-1" id="titleF" style="color:#FFFF1C">VI. Future</h2>
+
         <h2 class="content-1" id="titleF" style="color:#FFFF1C">VI. Future</h2>
 
         <div class="modelingPartContent" id="partF">
 
         <div class="modelingPartContent" id="partF">
 
            
 
            

Revision as of 08:17, 15 October 2016

Software—Toxin selection

I. Purpose

To prove the concept of Pantide, we wanted to select three existing distinct spider toxin peptides with probable oral toxicity against the testee-Spodoptera litura(Tobacco cutworms). For the actual application of Pantide we, we needed some more knowledge base of peptides which have different molecular targets to promote Pantide applying to other orders of insects, and a different toxic mechanism to regularly alternate so as to avoid drug resistance.

To date, about 1500 toxin peptides from 97 spider species have been studied, though the number of spider toxin peptides is conservatively estimated up to 10 million. [1] So, our purpose is to establish a database collecting the information of those peptides, such as molecular target, taxon, toxicity, sequence. According to the database, if we first choose a target insect, then we can easily find out groups of suitable peptides used as Pantide. Therefore, we also need to create a method to select peptides from the database.

II. Method

III. Step 1: Crawler

IV. Step 2: Filter

V. Step 3: Selection

VI. Future