Also check if you have correctly estimated no. of molecules in asymmetric
unit.

On Fri, May 21, 2010 at 4:58 PM, Tim Gruene <[email protected]> wrote:

> Dear  intekhab,
>
> a few suggestions:
> - are you sure of the space group or might there be alternatives?
> - is you protein globular or modular, i.e., is it worth running MR with
> stable
>  subdomains one after the other?
> - try a poly-alanine model (e.g. chainsaw can do this for you, pdbset
> probably,
>  too)
> - did you get overloads? If so, collect a low resolution pass to get
> correct
>  intensities even at the poor resolution end.
> - what is your low resolution limit? Did you use the default or could you
> extend
>  it?
> - did your crystal(s) suffer from radiation damage? It might be worth
> collection
>  only a complete data set with not too high multiplicity.
>
> Good luck, Tim
>
> On Fri, May 21, 2010 at 08:01:10PM +0900, intekhab alam wrote:
> > Hi all
> > I am trying to do molecular replacement with low resolution (4Å) using
> > Molrep and Phaser.
> >
> > Overall R-factor is 11.3%, completeness 95.4%, I/sigma 2, and Chi^2 0.95.
> >
> > Identities between my protein and templates were more than 80%.
> >
> > I couldn’t get correct solution.
> >
> > Rotation function, translation score, and contrast were low, and they had
> no
> > significance, though I changed the range of resolution.
> >
> > Molrep suggested solution coordinates clashed with symmetry molecules.
> >
> > I tried MR after remove clashed regions, but another clashes happened.
> >
> > In the case of phaser, there were many clashes, too.
> >
> > Please, give me any suggestion.
> > Should I concern about any options when I run MR programs?
> >
> > Hope you guys will be interested to answer!!!!!!
> > Thanks in advance
> >
> >
> > --
> > INTEKHAB ALAM
> > LABORATORY OF STRUCTURAL BIOINFORMATICS
> > KOREA UNIVERSITY, SEOUL
>
> --
> --
> Tim Gruene
> Institut fuer anorganische Chemie
> Tammannstr. 4
> D-37077 Goettingen
>
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