Quick navigation:        Home   |    Site Map   ||    References   |    Biography   ||    Copyright   |    Other copyright   |    Contact us   |   
Protein structure
 

Re: [ccp4bb] an over refined structure

 

Basic tutorials:
 
 

CCP4bb navigation

CCP4bb <-- 2008 <-- February 2008 <-- 08 February 2008
Previous message:
Subject: protein crystallography position at Nottingham University
From: Emsley Jonas Jonas {- dot -} Emsley {- at -} NOTTINGHAM {- dot -} AC {- dot -} UK
Date: 2008-02-08
Next message:
Subject: Re: Tag, you're in! Flag, V5, etc
From: Artem Evdokimov artem {- at -} XTALS {- dot -} ORG
Date: 2008-02-08


Subject: Re: an over refined structure
From: Bart Hazes bart {- dot -} hazes {- at -} UALBERTA {- dot -} CA
Date: 2008-02-08

Dale Tronrud wrote:
> price@UCHICAGO.EDU wrote:
> > Rotational near-crystallographic ncs is easy to handle this way, but
> > what about translational pseudo-symmetry (or should that be
> > pseudo-translational symmetry)? In such cases one whole set of spots is
> > systematically weaker than the other set. Then what is the
> > "theoretically correct" way to calculate Rfree? Write one's own code to
> > sort the spots into two piles?
> > Phoebe
> >
>
> Dear Phoebe,
>
> I've always been a fan of splitting the test set in these situations.
> The weak set of reflections provide information about the differences
> between the ncs mates (and the deviation of the ncs operator from a
> true crystallography operator) while the strong reflections provide
> information about the average of the ncs mates. If you mix the two
> sets in your Rfree calculation the strong set will tend to dominate
> and will obscure the consequences of allowing you ncs mates too much
> freedom to differ.

I haven't had to deal with this situation but my first impression is to
use the strong reflections for Rfree. For the strong reflections, and
any normal data, Rwork & Rfree are dominated by model errors and not
measurement errors. For the weak reflections measurement errors become
more significant if not dominant. In that case Rwork & Rfree will not be
a sensitive measure to judge model improvement and refinement strategy.

A second and possibly more important issue arises with determination of
Sigmaa values for maximum likelihood refinement. Sigmaa values are
related to the correlation between Fc and Fo amplitudes. When half of
your observed data is systematically weakened then this correlation is
going to be very high, even if the model is poor or completely wrong, as
long as it obeys the same pseudo-translation. If you only use the strong
reflections for Rfree I expect that should get around some of the issue.

Of course it can be valuable to also monitor the weak reflections to
optimize NCS restraints but probably not to drive maximum likelihood
refinement or to make general refinement strategy choices.

Bart


==============================================================================

Bart Hazes (Assistant Professor)
Dept. of Medical Microbiology & Immunology
University of Alberta
1-15 Medical Sciences Building
Edmonton, Alberta
Canada, T6G 2H7
phone: 1-780-492-0042
fax: 1-780-492-7521

==============================================================================

CCP4bb navigation

CCP4bb <-- 2008 <-- February 2008 <-- 08 February 2008
Previous message:
Subject: protein crystallography position at Nottingham University
From: Emsley Jonas Jonas {- dot -} Emsley {- at -} NOTTINGHAM {- dot -} AC {- dot -} UK
Date: 2008-02-08
Next message:
Subject: Re: Tag, you're in! Flag, V5, etc
From: Artem Evdokimov artem {- at -} XTALS {- dot -} ORG
Date: 2008-02-08



ProteinCrystallography.org: Copyright 2006-2007 by Quid United Ltd