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Titlebook: Biological Magnetic Resonance; Lawrence J. Berliner,Jacques Reuben Book 1990 Springer Science+Business Media New York 1990 DNA.electron sp

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Methods of Proton Resonance Assignment for Proteins,by the advent of site-directed mutagenesis and the resulting ease with which variant proteins can be produced. In the last few years, NMR spectroscopy has been called upon with increasing frequency for the necessary structural information.
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Methods for Suppression of the H2O Signal in Proton FT/NMR Spectroscopy,nd Jandetzky, 1981). Although much can be learned about the nonexchangeable protons from FT/NMR conducted in D.O solution, exchangeable protons (e.g., base-pair protons in RNA and DNA) can obviously be observed only in H.O. Even in D.O, the residual HDO signal can be large enough to obscure signals at or near the HDO peak.
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Structure Determination via Complete Relaxation Matrix Analysis (CORMA) of Two-Dimensional Nuclear the extent of secondary structure (local conformational properties such as .-helix and .-sheet). At best it is possible to obtain a measure of some of the distances within the molecule. However, with the possible exception of nuclear magnetic resonance, a high-resolution structural model is not yet attainable with any of these methods.
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Book 1990opical, authoritative chapters on new aspects of biological magnetic resonance. As always, we try to present a diversity of topic coverage in each volume, ranging from applications of in vivo magnetic resonance to more fundamental aspects of electron spin resonance and nuclear magnetic resonance. Ph
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Eigenschaften der Klebschichten,by the advent of site-directed mutagenesis and the resulting ease with which variant proteins can be produced. In the last few years, NMR spectroscopy has been called upon with increasing frequency for the necessary structural information.
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https://doi.org/10.1007/3-540-31223-4nd Jandetzky, 1981). Although much can be learned about the nonexchangeable protons from FT/NMR conducted in D.O solution, exchangeable protons (e.g., base-pair protons in RNA and DNA) can obviously be observed only in H.O. Even in D.O, the residual HDO signal can be large enough to obscure signals at or near the HDO peak.
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