On Wed, 6 Oct 2004, Goel, Manisha wrote: >Hi All, > >I am trying to build Profile HMM for a couple of protein domain families >(as defined in SCOP). >For building a Multiple sequence alignment, I have picked up related >members from PDB, but since the PDB often contains many structures of >the same protein (with multiple ligands or so), my alignments have >multiple copies of the same/highly similar sequences. > >Will the high redundancy of such an alignment effect the HMM model >quality ? >Since I will not be using these HMMs to look for distant relationships >but only confine myself to studying the members within a family .. I was >assuming this should not be problem. >Any suggestions ? Why do you want to use the HMM in this case? You could try using hmmer without calibrateing the modle. > >Thanks, >-Manisha >