Hello, everyone,
I have solved the structure of heme containing protein using anomalous signal from Fe atom (~1.739 anstroms) and further refined it using native dataset (0.9 angstroms).
Structure was solved in AutoSol. The question is "What is the best way to deposit mtz with both datasets?"
Should I merge and scale them simultaneously or can I deposit output file from AutoSol overall_best_refine_data.mtz, which contains F,FP, Rfree and HL coefficients?
P.S.: please, respond in PM, I have only digest subscription on phenixBB.

Thank you in advance!
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Evgenii Osipov
Laboratory for Biocrystallography, 
Department of Pharmaceutical Sciences, 
KU Leuven O&N2