I saw this post:
http://zhanglab.ccmb.med.umich.edu/bbs/?q=node/2325
Has any progress been made since 2013?
I ask because I have several hundred small peptide sequences (10-20aa each) for which I'd like to get predicted structures. However, their sequences were randomly generated (and then ran through a screen), thus they have minimal homology to natural proteins, and I-TASSER would not work.
Thanks :)
-Eric