Hydrogen bond Subject

The simulation (Lu et al., 1998) suggested how Ig domains achieve their chief design requirement of bursting one by one when subjected to external forces. At small extensions, the hydrogen bonds between strands A and B and between strands A and G prevent significant extension of a domain, i.e.. 

The family of serine proteases has been subjected to intensive studies of site-directed mutagenesis. These experiments provide unique information about the contributions of individual amino acids to kcat and KM. Some of the clearest conclusions have emerged from studies in subtilisin (Ref. 9), where the oxyanion intermediate is stabilized by t>e main-chain hydrogen bond of Ser 221 and an hydrogen bond from Asn 155 (Ref. 2). Replacement of Asn 155 (e.g., the Asn 155— Ala 155 described in Fig. 7.9) allows for a quantitative assessment of the effect of the protein dipoles on Ag. ... 

Wilson (1974) emphasized the importance of wetting the substrate surface. Later, as the reaction proceeded, these hydrogen bonds would be replaced by ionic salt bridges. Wilson stressed the importance of the polymeric nature of these cements in adhesion. Their polymeric nature allowed interfacial gaps between cement and substrate to be bridged and also provided a multiplicity of bonds. Under oral conditions, where the substrate is subject to change, adhesive bonds will be broken, but if there are a multiplicity of these, attachment of the cement to the substrate will endure and allow broken bonds to be re-established. It is significant that... 

The species HjO is subject to further hydration in the usual manner. Its primary sheath contains three water molecules linked through electrostatic forces, and in part through hydrogen bonds (i.e., the ion with its primary solvation sheath can be formulated as H9O4+). 

In a broad sense, one may include the Free-Wilson equation within the class of linear free energy relationships (LFER). It is also subjected to the assumption of additivity of the contributions to the biological activity by substituent groups at different substitution sites. The assumption requires, for example, that there is no hydrogen bonding interaction between the various substitution groups. 

Similarly to peroxycarboxylic acids, DMDO is subject to cis or syn stereoselectivity by hydroxy and other hydrogen-bonding functional groups.93 However a study of several substituted cyclohexenes in CH3CN —H20 suggested a dominance by steric effects. In particular, the hydroxy groups in cyclohex-2-enol and... 

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