Rolf Huehne wrote:

>
>In the case of PDB entry '4otb' there are 6 different biomolecules which
> all look very similar. Each biomolecule consists of different sets of 2
>chains (out of 12) from the asymmetric unit plus 2 copies of these
>chains generated by symmetry operations. So in the end you will have 6
>slightly different hexamers if you generate all biomolecules.
>
>  
>
And would you want to generate them all at the same time? Where do these 
different hexamers come from?
  

>As far as Bob has described the filter options yet, I don't think that
>it is currently possible to apply only a subset of the symmetry
>operations of a specific biomolecule. So with the virus capsid you would
>always get 60 copies of whatever you selected by the filter (e.g. only 1
>chain out of 3) into a single model/frame. And if you wanted to display
>only only one half of the capsid you could use for example the following
>command:
>
>  
>
Right, but this could be extended to include only specific BIOMT records.

>  display symop<=30
>
>How this half would really look like would of course depend on the order
>of the symmetry operations (e.g.: a ball might look afterwards like a
>ball with holes and not like one half of a ball).
>
>Regards,
>Rolf
>
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-- 
Robert M. Hanson
Professor of Chemistry
St. Olaf College
Northfield, MN
http://www.stolaf.edu/people/hansonr


If nature does not answer first what we want,
it is better to take what answer we get. 

-- Josiah Willard Gibbs, Lecture XXX, Monday, February 5, 1900



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