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Clock structure

Figure 10.6 STM images of the Ni(l 11) (5 /3 x 2)S phase and a model for the structure proposed to explain the decreased density of nickel within the islands, (a) 15.0 x 16.5 nm image showing the three possible domains of the (5 /3 x 2)S structure the brighter part of the image corresponds to an adlayer that has developed on top of a nickel island formed during H2S adsorption, (b) 1.8 x 2.9 nm atomically resolved image of the (5 /3 x 2)S structure, (c) Proposed clock structure for the (5 /3 x 2)S phase that accounts for the reduced nickel density in the sulfur adlayer. (Reproduced from Refs. 23 and 25). Figure 10.6 STM images of the Ni(l 11) (5 /3 x 2)S phase and a model for the structure proposed to explain the decreased density of nickel within the islands, (a) 15.0 x 16.5 nm image showing the three possible domains of the (5 /3 x 2)S structure the brighter part of the image corresponds to an adlayer that has developed on top of a nickel island formed during H2S adsorption, (b) 1.8 x 2.9 nm atomically resolved image of the (5 /3 x 2)S structure, (c) Proposed clock structure for the (5 /3 x 2)S phase that accounts for the reduced nickel density in the sulfur adlayer. (Reproduced from Refs. 23 and 25).
Knowledge of the detailed mechanism underlying circadian rhythms continues to be refined as new experiments reveal novel facets of the oscillatory machinery. Thus, a link has recently been established between chromatin structure and the circadian oscillatory mechanism. The CLOCK protein indeed functions as a histone acetyltransferase [116]. This enzyme activity is required for oscillations so that histone modification and the associated chromatin remodeling are implicated in the origin of circadian rhythmicity. [Pg.271]

J. Cooke and E. C. Zeeman, A clock and wavefront model for control of the number of repeated structures during animal morphogenesis. J. Theor. Biol. 58, 455 76 (1976). [Pg.293]

Laboratory support is carried out by the clinical diagnostic laboratory and laboratory of tissue typing. The equipment of clinical diagnostic laboratory allows carrying out hematological, biochemical investigations for the structural subdivisions of the Center, coagulometry, analysis of the acid-alkali state, the electrolytes of blood and several other researches in the round-the-clock mode. [Pg.256]

Fig. 12. Asymmetry of the DNA phosphodiester backbone trace as seen in the Oak Ridge NCP structural model (PDB access code lEQZ). No attempt has been made to regularize the geometry of the DNA positions of phosphates are based solely on the experimental electron density. Here the two DNA gyres are overlaid, with the 72 bp ventral gyre in red and the 73 bp dorsal gyre in blue. The minor groove positions facing the histone core are numbered sequentially from the dyad axis. The most pronounced asymmetry is seen in position 2 (10 o clock). Fig. 12. Asymmetry of the DNA phosphodiester backbone trace as seen in the Oak Ridge NCP structural model (PDB access code lEQZ). No attempt has been made to regularize the geometry of the DNA positions of phosphates are based solely on the experimental electron density. Here the two DNA gyres are overlaid, with the 72 bp ventral gyre in red and the 73 bp dorsal gyre in blue. The minor groove positions facing the histone core are numbered sequentially from the dyad axis. The most pronounced asymmetry is seen in position 2 (10 o clock).
The Jencks clock, as well as pulse radiolysis experiments, indicate that oxocarbenium cations often can be quite stabilized, with a half-life on the order of milliseconds. For example, at room temperature, the structures shown here (left to right) have respective lifetimes of... [Pg.393]

Clock oscillation occurs first at a cellular level. The clock genes so far identified in mammals are structurally similar to those in Drosophila (Young Kay 2001). This suggests that mammals and Drosophila utilize similar components to generate circadian ( 24 h) rhythms. Mammalian clock research is now showing whether the core feedback loop of clock genes speculated to be present in Drosophila (Hardin et al 1990) is also conserved in mammals. [Pg.162]


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