Fri Sep 26 14:07:15 PDT 2014
protein with various resolutions (2.8 â 1.2Ã
). The apo-structure is known
and well refined. The cell constants are fairly similar but not in all
cases identical, hence I would prefer a MR run prior to the refinement.
I am sure this can somehow be realized with some shell-script but maybe
there is some more sophisticated way of realising this?
I would also be happy for partial solutions to the problem.
More information about the phenixbb