addressing symmetric shadows
|Opened on:||Saturday, February 9, 2013 - 08:07|
|Last modified:||Saturday, February 9, 2013 - 18:50|
recipes would be much more efficient if we could automatically terminate bands
on symmetric partners of th protein.
for a dimer we could number the protein itself 1 to N and the shadow N+1 to 2N
with a correspondance p to N+p.
for a trimer N+1 to 2N and 2N+1 to 3N.
I don't know if this is feasible but i assume it should'nt be so difficult.