Hello,
I’m working on a small protein and it made sense to fold peaks in the indirect 15N dimensions (2D, 3D). I have an NHSQC which does not have folded peaks and then one with a narrower 15N SW where I have ‘folded’ peaks. How should I best peak the peaks and set-up the project so CCPN will handle the ‘true’ 15N shifts of the folded peaks correctly?
Thanks, Mark
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