Greetings, 

Previously I have created a program which takes a sequence of hydrophobic or
hydrophilic amino acids and folds it based of the HP protein folding model.
The folded coordinates are given and displayed in a x-y-z grid format (as in
an amino acid can only be located on integer x, y, z coordinates; no
decimals). A typical folded protein resembles this:

http://ars.els-cdn.com/content/image/1-s2.0-S1476927108000327-gr2.jpg
http://ars.els-cdn.com/content/image/1-s2.0-S1476927108000327-gr2.jpg
http://ars.els-cdn.com/content/image/1-s2.0-S1476927108000327-gr2.jpg 

What I hoping to add is to use Jmol to display this protein. However,
instead of simply a ball representing the amino acid, I would like to show
each molecule of each amino acid. 

My current idea of how I would go about this is as such:

- Read in a real protein sequence ( Lys - Asp - Arg - etc ), and turn this
into a string of hydrophobic or hydrophilic amino acids for my program to
fold. 
- Once folded, replace each amino acid with it's actual molecules in Jmol,
to do this I might
     - programmatically create a .pdb file for Jmol to read. To do this I
would already have pdb files for all 20 amino acids stored, and displace
their atoms to the grid coordinate given from the existing program. However,
I would have to get the amino acids to be bonded together through peptide
bonds, which seems tricky. 

Before I step into this large project, I would just like to ensure I'm on
the right path and doing things the best/easiest way possible. I am quite
new to Jmol and would very much appreciate any suggestions or things to look
out for. If you have any questions, I am more than happy to answer them. 

Thank you for your time 
-- 
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