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<p>Dear Sir/Madam,<br>
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<p> I am using Chimara to display large proteins. It is very nice. 6DHO(PDB structure, see attachment) is a very recent PSII structure consisting both S2 and S3(richer) states, which are highly overlapped in the raw data. I am urgently wondering how
can I separate S3 out from the S2/S3 mixture by Chimera, especially the OEY cluster and all its ligands? Thank you very much!<br>
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<p>Best wishes<br>
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