Hi,I believe it is not important as long as you run a proper scan of the
crystal. Both forms will allow proper phasing.
This is very well described in a paper from Thomazeau et al.
here is the reference

MAD on threonine synthase: the phasing power of oxidized selenomethionine.
Acta Crystallogr D Biol
Crystallogr.<javascript:AL_get(this,%20'jour',%20'Acta%20Crystallogr%20D%20Biol%20Crystallogr.');>
2001
Sep;57(Pt 9):1337-40. Epub 2001 Aug 23.

Cheers,

Pascal Egea, PhD
Post Doctoral Researcher
UCSF Department of Biochemistry and Biophysics
Stroud laboratory






On Mon, Feb 9, 2009 at 10:27 AM, aka akaka <druida...@hotmail.com> wrote:

>  Dear All
> I would like to know whether oxidation of Se entails any problem for SAD or
> MAD experiments and/ or how to resolve it. Cannot use DTT or reducing agents
> in my protein (extracellular and disulphide bonds are important).
> Thanks
>
> Dr. R.Depetris
> Weill Cornell Medical College
>
>
>
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