> dipolar couplings (NMR). But even then one should always look at the
> structure model in the context of the experimental data. High
Is there an easy way to do this for NMR data? For x-ray data, it's
relatively straightforward to re-calculate a map using the deposited
model and amplitudes, which generally makes pretty clear which regions
of the model may have issues. But from my conversations with NMR people
there isn't an analogous process for NMR, short of re-refining against
the constraints (of course, it's possible that I was/am asking the wrong
question here).
Pete
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