On Tue, 17 May 2005, Gerard DVD Kleywegt wrote: >> In general how can a single structure be used to improve a multiple >> sequence alignment (if at all)? > >you can align sequences to a structure and have higher penalties for >insertions/deletions in regions of secondary structure (since we know they are >less likely to occur there). this is what we do in Indonesia >(http://xray.bmc.uu.se/dennis) I see. Do you use 'environment specific' substitution tables too? (I heard about these in the context of secondary structure and core vs. surface 'environments'). How much of an improvement in alignments do you get using these considerations? Cheers, Dan. > >--gerard > >****************************************************************** > Gerard J. Kleywegt > [Research Fellow of the Royal Swedish Academy of Sciences] >Dept. of Cell & Molecular Biology University of Uppsala > Biomedical Centre Box 596 > SE-751 24 Uppsala SWEDEN > > http://xray.bmc.uu.se/gerard/ mailto:gerard at xray.bmc.uu.se >****************************************************************** > The opinions in this message are fictional. Any similarity > to actual opinions, living or dead, is purely coincidental. >****************************************************************** >