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A X-ray diffraction

Based on Arnone A X-ray diffraction study of binding of 2,3-diphosphoglycerate to human deoxyhemoglobin. Nature 1972 237 146. Reproduced with permission.)... [Pg.45]

The dihydrogen molecule assumes a side-on terminal coordination. The W-H2 distance is 1.95 A (X-ray diffraction) or 1.89 A (neutron diffraction). The H-H distance is 0.75 A (X-ray diffraction) or 0.82 A (neutron diffraction), with respect to 0.74 A for molecular hydrogen in the gaseous state. [Pg.486]

Fig. 2. The histone octamer. The 3.1 A X-ray diffraction data model of Arents et al. [20] is shown in secondary structure cartoon format. The core of the histone octamer is well defined, but more than 30% of the histone sequence is in regions without secondary structure. These are unfortunately the most interesting regions in terms of epigenetic signaling. 25% of the molecule located in the N-terminal tails (and the C-termini of H2A) in the 3.1 A octamer structure has no interpretable electron density. Despite these limitations, this structure is sufficient to use as a starting model for molecular replacement phasing of the NCP. (Image courtesy of E. Moudrianakis.)... Fig. 2. The histone octamer. The 3.1 A X-ray diffraction data model of Arents et al. [20] is shown in secondary structure cartoon format. The core of the histone octamer is well defined, but more than 30% of the histone sequence is in regions without secondary structure. These are unfortunately the most interesting regions in terms of epigenetic signaling. 25% of the molecule located in the N-terminal tails (and the C-termini of H2A) in the 3.1 A octamer structure has no interpretable electron density. Despite these limitations, this structure is sufficient to use as a starting model for molecular replacement phasing of the NCP. (Image courtesy of E. Moudrianakis.)...
Figure5.47 (a) X-ray diffraction pattern (Cu Ka) of a commercial UBH4 sample (b) X-ray diffraction patter after the thermal desorption of hydrogen from the sample (a) (c) X-ray diffraction pattern of the sample upon reabsorption of the hydrogen. Figure5.47 (a) X-ray diffraction pattern (Cu Ka) of a commercial UBH4 sample (b) X-ray diffraction patter after the thermal desorption of hydrogen from the sample (a) (c) X-ray diffraction pattern of the sample upon reabsorption of the hydrogen.
Fig. 9.2.7 Characterization of the intermediate phase obtained in the reduction of Ni(OH)2 in ethylene glycol (a) x-ray diffraction pattern, and (b) structural model. (From Ref. 29.)... Fig. 9.2.7 Characterization of the intermediate phase obtained in the reduction of Ni(OH)2 in ethylene glycol (a) x-ray diffraction pattern, and (b) structural model. (From Ref. 29.)...
Fig. 14. (a) X-ray diffraction pattern of a rapid quenched sample with the nominal composition HoPd2B2C with typical fee reflexes, (b) Lattice constant a of the non-identified fee unit cell for different rapidly quenched samples of nominal composition / Pd2B2C (Freudenbeiger 2000). [Pg.225]

C4H9)4N]X, lies to the right under acidic conditions and in non aqueous solvent and is rather difficult to detect.7 (Ultracentrifugation solution molecular-weight determinations under several conditions are available.7) Attempts to grow single crystals of this product suitable for a X-ray diffraction structural analysis have been unsuccessful. [Pg.191]

The Mo2N-A X-ray diffraction powder pattern shows broad diffraction peaks, making slight variations of the a cubic unit cell parameter difficult to measure. Despite careful preparation the platelet morphology of the powder gives rise to preferential orientation and an increase in the 200 peak intensity relative to the 111 reflection (Figure 13.3). [Pg.419]

Figure 6. (a) X-ray diffraction pattern of the 10, form of poly d(l) poly(C) and (b) a pitch length of this structure viewed normal to (top) and along the helix axis (bottom,). Note the small positive tilt of the bases and the forward positioning of the base-pairs characteristic of the A-famity. [Pg.496]

Figure 7.9 (a) X-ray diffraction channel oscillation photograph of 2-decanone-urea showing host... [Pg.431]

Depth profiling of phase compositions in a hybrid LGM as revealed by (a) X-ray diffraction and (b) grazing-incidence synchrotron radiation diffraction. [Pg.148]

There are other factors affecting the intensity of the peaks on a x-ray diffraction profile of a powdered sample. We have analyzed the structure factor, the polarization factor, and the broadening of the lines because of the dimensions of the crystallites. Now, we will analyze the multiplicity factor, the Lorentz factor, the absorption factor, the temperature factor, and the texture factor [21,22,24,26],... [Pg.36]

Guinier, A. "X-Ray Diffraction in Crystals, Imperfect Crystals, and Amorphous Bodies" Freeman San Francisco, 1963 pp. 3-4. [Pg.28]

Figure A X-ray diffraction patterns of POD films pyrolyzed at HTT s below 1000 C. Figure A X-ray diffraction patterns of POD films pyrolyzed at HTT s below 1000 C.
The total volume of protein crystals is 25—65% water, and problems that are not yet completely resolved are the nature and location of the water molecules. However, much light is being shed on the problem by high-resolution (0.12—0.18 nm 1.2-1.8 A) X-ray diffraction studies, supplemented more recently by neutron diffraction studies (Kossiakoff, 1985). Edsall and McKenzie (1983) have made a tentative classification... [Pg.204]


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See also in sourсe #XX -- [ Pg.86 ]




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A X-ray diffraction patterns

A with X-ray diffraction

X-ray diffraction by a crystal

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