Can not you instead correct amide shifts in BMRB file, then
import them and create peak lists using this corrected shift
list...
> Date: Wed, 3 Oct 2012 01:57:37 +0100
> From:
[log in to unmask]
> Subject: Re: Shifting peaks
> To:
[log in to unmask]
>
> Hi,
>
> I asked this question before, but perhaps it didn't get
sent or I was too vague or it is so blatently obvious that I
should have been able to find it myself. Hopefully with
clarification someone might know what I am talking about and
take pitty on me...
>
> I have measured a series of spectra of a protein. There
are assignments on the BMRB and I have been able to create a
synthetic shift list for my spectra from an import. I have
corrected the 15N-HSQC peaks to line up with my sample, some
of which have significant changes in chemical shift due to the
different conditions of my sample.
>
> Now before I start trying to shift all the peaks in my
other spectra (NOESY, TOCSY, HNCA, HNCACB, etc.), is there a
way to 'correct' just the nitrogen and amide proton shifts of
the synthetic lists that I generate so I can reduce the amount
of searching I have to do?
>
> Kind regards,
>
> Tom Carruthers