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

--
Dr Rhys Grinter
Lab Head
Molecular Physiology of Microbial Pathogens (MP2) Lab
Monash University
+61 (0)3 9902 9213
+61 (0)403 896 767