hi I have a problem with my bioinformatic exam : I have to do homology modelling and I have my fasta sequence of my 1APM protein ,using swissPDB I load it in swissmodl , load raw sequence and I see it as a long elich. I use edit select against exPDB and I select a 50% identity protein 1ftoA and I have both proteins shown on the screen. Now what I have to do is studyng thereading and the overlapping of my proteins and RMS. someone can help me? thanks