.refine gives Rree-R label that other
program could not recognize.
Could anyone please help me to solve this problem?
Thank you very much in advance,
Best,
Vinson, Liang
Dear all,
Thank you very much for your suggestions.
I try Pavel's easy method. Hopefully, the result from phenix.model_vs_data
would be enough for PDB.
Best wishes,
Vinson
发件人: Pavel Afonine
收件人: PHENIX user mailing list
抄 送: Vinson LIANG
发送日期: 2010/10/22 (周五) 12:
2, 2010 at 02:33:03PM +0800, Vinson LIANG wrote:
> >
> >
> > Dear all,
> >
> >
> >
> >
> > Thank you very much for your suggestions.
> >
> > I try Pavel's easy method. Hopefully, the result from p
inked glycosylation.
All the best,
Vinson
发件人: Savvas Savvides
收件人: Vinson LIANG
抄 送: CCP4BB@JISCMAIL.AC.UK
发送日期: 2010/11/24 (周三) 9:27:31 下午
主 题: Re: [ccp4bb] Strange density on Serine oxygen.
Hi Vinson
Beyond the possibility for another type of residue as al
s Savvides
收件人: Vinson LIANG
抄 送: CCP4BB@JISCMAIL.AC.UK
发送日期: 2010/11/24 (周三) 9:48:28 下午
主 题: Re: [ccp4bb] Strange density on Serine oxygen.
Hi Vinson
is O-glycosylation possible at all given the origin of the protein and the
expression system used?
best
Savvas
On 24 Nov 2010, at 14:42, Vin
lation
> (http://www.cbs.dtu.dk/databases/OGLYCBASE/).
>
> best regards
> Savvas
>
>
> Savvas Savvides
> Unit for Structural Biology @ L-ProBE
> Ghent University
> K.L. Ledeganckstraat 35, 9000 Ghent, Belgium
> Ph. +32 (0)472 928 519 http://www.LProBE.ugent.be/xra
t wishes,
Vinson Liang
Dear all,
Sorry for this silly biochemistory question. Thing is that I have a reversible
epimerase and I want to mutate it into an inreversible one. However, I have
been told that the ΔG of a reversible reaction is zero. Which direction the
reaction goes depends only on the concentration of
to break the EQ of the reaction. So I think the best thing
I could do is to take Mickael's suggestion and add another enzyme to change the
concentration of one substrate.
However, Lijun's comment do open my mind.
I really appreciate all your help,
Best Regards,
Vinson Liang