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Six of the proteins have stabilities equal to or up to 7 kcal/mol greater than their wild-type counterparts, and four of the proteins have NMR spectra consistent with a well-packed, rigid structure.
Metabolites have NMR spectral signatures characterized by their chemical structures.
The only Si O P bonds in phosphosilicate glasses that have been unequivocally assigned by means of J-coupling NMR spectroscopy have NMR resonances, which, to the best of our knowledge, have never been reported in the literature on phosphated zeolites.
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The 75 nt B. mori R2 retrotransposon pseudoknot has NMR spectra that agree well with those of a 74 nt construct originally used to identify the same pseudoknot.
The subset analysis showed that 9 of 10 proteins had NMR ensembles exhibiting almost no or small flexibility, in contrast to CABS-flex or MD predictions (the exception was 1pcp, which has a small amount of secondary structure only).
We have used NMR techniques to study the structural effects of the R249S mutation.
So it's quite clear what this structure is, that it's this quinoid dimer, once you have the NMR to see it.
We have used NMR to study the effects of peptide binding on the N-terminal p53-binding domain of human MDM2 (residues 25 109).
Since MA has been reported to be a component of the preintegration complex (PIC), we have used NMR to probe its interaction with other PIC components.
Now, Sekhar et al. have used NMR to document the dynamics of immature SOD1 proteins.
This pattern features two coexisting equal populations of Gln residues that have different NMR signals.
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