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CCP4BB  May 2011

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Subject:

Re: Low resolution refinement

From:

David Schuller <[log in to unmask]>

Reply-To:

[log in to unmask]

Date:

Thu, 19 May 2011 12:39:59 -0400

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (62 lines)

This reminds me of:

Pig heart short chain L-3-hydroxyacyl-CoA dehydrogenase revisited: 
Sequence analysis and crystal structure determination
Barycki JJ, O'Brien LK, Birktoft JJ, Strauss AW, Banaszak LJ
Protein Science (Oct 1999) Vol 8, pp 2010-2018.

In which the protein in question also had one monomer forming a dimer 
about a crystallographic axis, and two monomers forming a dimer 
elsewhere in the asymmetric unit.

A portion of the molecule had messy density, which caused difficulties 
literally for decades. The eventual solution was to switch to a 
different species (human). After which, a MR solution of the original 
porcine data was possible. I believe the disorder was judged to be 
intrinsic.



On 05/19/11 09:02, Joane Kathelen Rustiguel wrote:
> Dear all
>
>
> I am refining a structure at 3.4 A resolution that contains 3 molecules in the
> a.u. The chain A sits on a 2-fold crystallographic axis forming the dimeric
> functional structure expected for this class of proteins. The other two chains
> B and C, which also form the functional dimer, seem to be, somehow, a lot more
> flexible than chain A. As a result, whereas the electron density map, b-factor
> and geometry for chain A is pretty reasonable for a 3.4 A resolution
> structure, the refinement for the other two chains (B and C) does not behave
> well. Even playing with different weights for geometry, analysing different
> levels of 2Fo-Fc/Fo-Fc maps, using NCS, TLS, etc..., nothing works. The map
> for the helical regions is ok, but the electron density map for strands and
> loops of chains B and C are broken along the main chain, B-factors are really
> high, and the geometry keeps being distorted.
>
> Right now, the R-factor and R-free are 24.2 and 28.6, respectively.
>
> Any suggestions in how to proceed the refinement?
> And even a more difficult question, how do we report this type of structure?
> How do we deposit those coordinates? We can certainly use chain A as a model
> to perform interesting studies of structure-function relationship, but we know
> that chain B and chain C have problems.
>
> Any help will be greatly appreciated.
>
> Regards
>
> Joane
>
>


-- 
=======================================================================
All Things Serve the Beam
=======================================================================
                                David J. Schuller
                                modern man in a post-modern world
                                MacCHESS, Cornell University
                                [log in to unmask]

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