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protein with various resolutions (2.8 – 1.2Å). 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.
 

Best regards
 

Eike