I take it that the datasets are from different crystals. Are the crystallisation conditions the same? I can't spot any signs of a difference in indexing (but I may be wrong) so they look like different crystal forms. Are the processing statistics good for both? Is this a case for molecular replacement or experimental phasing? You could work with best diffracting one and solve that one first and then use it to solve the other by molecular replacement. Hope some of this helps.
Sent from Yahoo Mail on Android On Sun, 8 Sep 2019 at 12:16, Prerana G.<[email protected]> wrote: Dear all, We have two data sets of a protein with the following parameters:1. Space group P212121 a=61.0, b=100.34, c=133.23 No. of molecules in ASU - 2 2. Space group P212121 a=58.33, b=62.86, c=109.45 No. of molecules in ASU - 1 Can we use them as two different structures? Regards,Prerana To unsubscribe from the CCP4BB list, click the following link: https://www.jiscmail.ac.uk/cgi-bin/webadmin?SUBED1=CCP4BB&A=1 ######################################################################## To unsubscribe from the CCP4BB list, click the following link: https://www.jiscmail.ac.uk/cgi-bin/webadmin?SUBED1=CCP4BB&A=1
