Hi Marco,

A few suggestions that I like to follow for MAD experiments:

Before everything, check you have at least about 1 SeMet per 100 residues Then before crystallisation check by MassSpec that SeMet is properly incorporated in your protein After crystallisation collect first on the peak with (very) high redundancy and as little/gentle dose as possible Collecting the other wavelengths should give you better starting phases/maps, which might be very helpful at your resolution of 2.8 (especially if it is a very anisotropic 2.8...)

Automated pipelines are so good nowadays, if you collect good data they should solve it without problems (as long as your crystal is not suffering from other pathologies like twinning or pseudosymmtries).

Good luck!

D


On 2024-05-14 01:17, Marco Bravo wrote:
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Hello all,
I have a data collection trip next week and plan to collect data on
selenomethionine derivative crystals at the al831 beamline. Are there
any resources, tips, tutorials, literature etc. That you can recommend
to help me prepare for these experiments. Also is there a way to plug
in the experimental data into ccp4 cloud to do the automatic structure
solution? Do I need native and derivative data to solve the structure?
Last trip I collected a seemingly 2.8 angstrom resolution data on a
crystal of the native protein but could not get a solution depsite
extensive molecular replacement attempts. It seems that assigning a
space group for the crystals has been troublesome as well. here is my
last thread I posted about the issue for reference.

https://www.jiscmail.ac.uk/cgi-bin/wa-jisc.exe?A2=ind2402&L=CCP4BB&O=D&X=CCE6DFA19FA3D40346&Y=mbrav005%40ucr.edu&P=112302

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