Hi PHENIX BB,
I'm currently refining a structure with 3Fe4S clusters into some high resolution cryoEM maps (1.57 Ang). However, refinement messes up the Fe4S cluster, by moving the existing Fe and S atoms into the wrong positions in the density.
Is anyone aware of this issue and/or knows of a simple way to prevent this from happening?
Cheers,
Rhys
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Dr Rhys Grinter
Lab Head
Molecular Physiology of Microbial Pathogens (MP2) Lab
Monash University
+61 (0)3 9902 9213
+61 (0)403 896 767