Interactive modelling (MASSHA, SASpy) and global minimization programs (SASREF, BUNCH, CORAL, GLOBSYMM)
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So my SAXS model differs greatly from current structures published for my protein. So I wanted to use Sreflex to try estimate what conformational changes would occur to form this new conformation seen in solution from my SAXS data. However Sreflex produces 10 models. How can I interpret the different models?Which values are of more importance, less breaks, clashes, rmsd chi squared. Which values take precedence in determining the more accurate models?