Titlebook: NMR as a Structural Tool for Macromolecules; Current Status and F B. D. Nageswara Rao,Marvin D. Kemple Book 1996 Plenum Press, New York 199

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Incorporating Motional Properties into the Interpretation of Three-dimensional Solution Structures,oscopy is uniquely suited to the determination of high resolution solution structures, and has vast potential as a means for examining molecular dynamics because a wide array of nuclear sites within a molecule can be assayed at a variety of different time scales. However, at present we are in the mi

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Panel Discussion,Dr. Rao has asked me to moderate this session. I told him I have very little to say on this topic and then he asked me at least if I could moderate it. As a consequence, we sat together yesterday night and today at noon and planned a little as to how to organize this. We agreed that we have about fi

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Recent Developments in Protein NMR Spectroscopy,R pulse sequence methodology and improvements in spectrometer hardware. Although the concepts on which modern NMR pulse sequences rely have been well understood for over 40 years, interesting and useful applications of these old ideas are driving the field of biomolecular NMR to a level where it is

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Towards the Accurate Measurement of Internuclear Distances in Biological Macromolecules by Suppressthrich, 1986; Neuhaus and Williamson, 1989). Cross-peak intensities .. obtained by two-dimensional .uclear Overhauser .ffect .pectroscopy (NOESY) (Anil Kumar et al., 1980; Wüthrich, 1986) can be related to proton-proton distances r.. Cross-relaxation processes stemming from the dipole-dipole interac

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NMR of Symmetrical Assemblies of Self-Recognizing Oligonucleotides, intimately associated, with their hemi-protonated C·C. base pairs face-to-face and fully intercalated, in a so-called “.”. This structure, first observed in the tetramer of d(TCCCCC)., is also formed by other sequences, including the very short d(TCC). In all cases, the four strands appear as ident

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