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Co structure

Figure 8.6 STM image of Ni (11 l)-c(4 x 2) CO structure with (a) (4 x 2) (white) and c(4 x 2) (black) unit cells shown with corresponding corrugation line scan (0.2 A full scale) (b) similar to (a) under different tunnelling conditions and corresponding line scan (0.3 A full scale). (Reproduced from Ref. 20). Figure 8.6 STM image of Ni (11 l)-c(4 x 2) CO structure with (a) (4 x 2) (white) and c(4 x 2) (black) unit cells shown with corresponding corrugation line scan (0.2 A full scale) (b) similar to (a) under different tunnelling conditions and corresponding line scan (0.3 A full scale). (Reproduced from Ref. 20).
Structural studies on Ago proteins revealed that the so-called MID domain binds the 5 end of the guide strand (39,40). Because of its central localization in the Ago protein, this domain has been named MID domain. Crystal co-structures and Kj measurements of the MID domain in combination with all four nucleotides at the 5 end revealed that uridine (U) binds with the highest affinity to the MID domain, adenosine (A) with a slightly reduced affinity, and cytosine (C) and guanosine (G) with more than tenfold less affinity (41). Therefore, siRNA guide (antisense) strands should ideally contain a U or A at the 5 end. C and G should be avoided. For the passenger (sense) strand 5 end, C and G should be selected in order to minimize strand incorporation (Fig. la). Based on our own unpublished data the nucleotide specificity is not only a tool to manipulate strand selection but siRNA strands with U or A at the 5 end show also a higher absolute affinity for Ago proteins and therefore are more likely to be potent siRNAs (see Notes 2 and 3). [Pg.65]

Castor oil [CO Structure (4.3)] is a triglyceride of ricinoleic (12-hydroxyoleic) acid about 90% of the fatty acid portion of the molecule consists of ricinoleic acid and 10% in the form of non-hydroxy acids consisting largely of oleic and linoleic acids. Small amounts of stearic and dihydroxystearic acids are also found in some industrial grades. [Pg.245]

The fastest way to obtain co-structures with a protein and fragments is to soak the fragments into existing crystals. Since each protein is unique, trial and error will be necessary to deduce the conditions where your protein crystals are stable and the fragments are suitably soluble (referred to as the protein stabilization buffer) (rrrNote 9). [Pg.247]

Tonkin ML, Roques M, Lamarque MH et al (2011) Host cell invasion by apicomplexan parasites insights from the co-structure of AMA1 with a RON2 peptide. Science 333(6041 ) 463-467... [Pg.224]

Further structural work is required to determine if this proposed COS structure is correct. However, if correct, then these B. japonicum LPSs have a similar ManiKdo2 inner core structural arrangement as described above for the R. leguminosarum, R. etli, and several Agrobacterium LPSs. [Pg.349]

R. etli strains. LpcB adds the external Kdo residue from CMP-Kdo to the Gal of the R. leguminosarum COS structure. An LpcB ortholog was found on pSymB of... [Pg.360]

In summary, the results of this section demonstrate that by application of XPS, adsorbate structures and coverages can be obtained at pressures of the order of a millibar. Thus, the pressure range in XPS has been expanded by at least five orders of magnitude. Even at these relatively high pressures, CO structures were found to be similar to those known from UHV investigations, but obtained at low temperatures (<300 K). CO on Pd(lll) adsorbs in threefold hollow, bridge, and on-top sites. Bukhtiyarov and coworkers (Bukhtiyarov et al., 1994 Kaichev et al., 2003) did not find any indications of CO dissociation or metal carbonyl formation under the experimental conditions (Bukhtiyarov et al., 2005 Kaichev et al., 2003). [Pg.234]

In all the listed structures the CO or NO molecule is believed to adsorb perpendicular to the surface with the oxygen end away from the surface. For CO structures with multiple non-equivalent adsorption sites these are listed on consecutive lines. If the metal layer spacing has been investigated this is listed after the adsorbate information.)... [Pg.157]

Activation of CO Structure Dependence and Trends as a Function of Metal... [Pg.128]

The adsorption of CO is probably the most extensively investigated surface process. CO is a reactant in many catalytic processes (methanol synthesis and methanation, Fischer-Tropsch synthesis, water gas shift, CO oxidation for pollution control, etc. (1,3-5,249,250)), and CO has long been used as a probe molecule to titrate the number of exposed metal atoms and determine the types of adsorption sites in catalysts (27,251). However, even for the simplest elementary step of these reactions, CO adsorption, the relevance of surface science results for heterogeneous catalysis has been questioned (43,44). Are CO adsorbate structures produced under typical UHV conditions (i.e., by exposure of a few Langmuirs (1 L = 10 Torrs) at 100—200 K) at all representative of CO structures present under reaction conditions How good are extrapolations over 10 or more orders of magnitude in pressure Such questions are justified, because there are several scenarios that may account for differences between UHV and high-pressure conditions. Apart from pressure, attention must also be paid to the temperature. [Pg.159]


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See also in sourсe #XX -- [ Pg.66 ]




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