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Right-handed crossing

When myofibrils are examined by electron microscopy, it appears that each one is constructed of two types of longimdinal filaments. One type, the thick filament, confined to the A band, contains chiefly the protein myosin. These filaments are about 16 run in diameter and arranged in cross-section as a hexagonal array (Figure 49-2, center right-hand cross-section). [Pg.557]

Murchie, A. I. H., Clegg, R. M., von Kitzing, E., Duckett, D. R., Diekmann, S., and Lilley, D. M. J. (1989). Fluorescence energy transfer shows that the four-way DNA junction is a right-handed cross of antiparallel molecules. Nature 341, 763—766. [Pg.185]

Consider now three knots, denoted by K, K , and K+. These three knots are identical under the cover Q, shown in Figure 3.6, and they differ only in their exposed parts, where they have a left-handed crossing, an avoided crossing, and a right-handed crossing, respectively. For any three such knots their Jones polynomials VK (t), VKo(t), and VK+(t) are interrelated by the equation... [Pg.77]

Figure 5.12 Examples of the characteristic graphs of the crossing patterns of three orthogonal views of the chain molecule backbone of the A.-Cro Repressor protein. The chain is oriented from the N-terminal to the C-terminal and the vertices of the graphs are labeled according to the handedness of the crossing - for left handed crossings, + for right handed crossings, 0 for the two terminals of the chain (no crossing). Figure 5.12 Examples of the characteristic graphs of the crossing patterns of three orthogonal views of the chain molecule backbone of the A.-Cro Repressor protein. The chain is oriented from the N-terminal to the C-terminal and the vertices of the graphs are labeled according to the handedness of the crossing - for left handed crossings, + for right handed crossings, 0 for the two terminals of the chain (no crossing).
FIGURE 9 A right-handed cross-over connection joining two paraiiei e-strands. Note the right-handed twist of the -strands when viewed aiong the strand axis. [Pg.166]

Equations (169) and (171), together with Eqs. (170), fomi the basic equations that enable the calculation of the non-adiabatic coupling matrix. As is noticed, this set of equations creates a hierarchy of approximations starting with the assumption that the cross-products on the right-hand side of Eq. (171) have small values because at any point in configuration space at least one of the multipliers in the product is small [115]. [Pg.698]

The porosity appears in the denominator of the right-hand side of the equaUty owing to the dependence of velocity on the available flow area, which is reduced from the total cross-sectional area by the factor n. [Pg.402]

The principle of double entry dates from the fifteenth century and is based on the premise that eveiy transaction involves a giver and a receiver of value. Double entiy requires that each transaction be entered into two accounts, the convention being that the account of the giver is credited and the account of the receiver is debited with the same amount of money, as noted in the journal. For convenience, each account is divided centrally, and the debit items are entered on the right-hand side. It is also usual to provide a cross-reference to the journ entiy so that errors and omissions can be checked. [Pg.837]

Connections between /3-strands are of two types—hairpins and cross-overs. Hairpins, as shown in Figure 6.27, connect adjacent antiparallel /3-strands. Cross-overs are necessary to connect adjacent (or nearly adjacent) parallel /3-strands. Nearly all cross-over structures are right-handed. Only in subtilisin and phosphoglucoisomerase have isolated left-handed cross-overs been identi-... [Pg.183]

For flavodoxin in Figure 6.32, identify the right-handed crossovers and the left-handed cross-overs in the parallel /3-sheet. [Pg.207]

Figure 51-5. Formation of a fibrin clot. A Thrombin-induced cleavage of Arg-Gly bonds of the Aaand B(3 chains of fibrinogen to produce fi-brinopeptides (left-hand side) and the a and p chains of fibrin monomer (right-hand side). B Cross-linking of fibrin molecules by activated factor XIII (factor Xllla). Figure 51-5. Formation of a fibrin clot. A Thrombin-induced cleavage of Arg-Gly bonds of the Aaand B(3 chains of fibrinogen to produce fi-brinopeptides (left-hand side) and the a and p chains of fibrin monomer (right-hand side). B Cross-linking of fibrin molecules by activated factor XIII (factor Xllla).
Unfortunately, in the VUV region no polarimetry data are available, but calculations indicate the degree of circular polarization achieved by the wiggler may be 80%, estimated to be no worse than 70% delivered at the experimental chamber [95, 96]. In PECD experiments, we have calibrated the polarization state by deduction from cross-comparison of results at a few fixed energies previously studied on the SU5 beamline where accurate polarimetry data was available [36]. Because the horizontal magnetic field array in the insertion device is electromagnetic, fast current reversal to switch left- and right-handed elliptical polarizations is possible, with the usual potential benefit for dichroism measurements. [Pg.303]

Figure 8.26. Equilibrium curve, optimal operation line, and optimal catalyst curves in an [ammonia] versus temperature plot for two different sets of conditions. Left-hand panel 420 °C, 80 bar, and 2 1 H2 N2 right-hand panel 450 °C, 200 bar, and 3 1 H2 N2. The crossing between the optimal catalyst curve for specific nitrogen bonding energy and the... Figure 8.26. Equilibrium curve, optimal operation line, and optimal catalyst curves in an [ammonia] versus temperature plot for two different sets of conditions. Left-hand panel 420 °C, 80 bar, and 2 1 H2 N2 right-hand panel 450 °C, 200 bar, and 3 1 H2 N2. The crossing between the optimal catalyst curve for specific nitrogen bonding energy and the...
For those cases when the cross section of the body has a relatively simple shape, the integral on the right hand side of this equation can be expressed through elementary functions. However, in more complicated cases, determination of the field is performed by numerical integration of Equation (4.19). [Pg.232]


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See also in sourсe #XX -- [ Pg.74 , Pg.128 ]




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