Sentence examples for binding to the tertiary from inspiring English sources

Exact(1)

Furthermore, this dye is non-fluorescent in solution but becomes brightly fluorescent upon binding to the tertiary structure of aggregated proteins [23].

Similar(59)

Linkages through the base or sugar preclude direct binding to these locations; therefore, fewer tertiary structures will be capable of binding to the target.

To improve our understanding of the contributions of these two types of interactions and the reasons for differential binding to the HDL2 and HDL3 subclasses, we now compare the binding of apoA-I variants with altered tertiary structural domain characteristics to HDL and lipid emulsion particles.

Interestingly, mutation of residue 163 increased both E2 and antibody binding, suggesting that this amino acid contributes to the tertiary structure of CD81 and its ligand-binding ability.

It shifts slightly upon binding of dUMP in the binary complex, but much more substantially following Raltitrexed binding in the tertiary complex.

As shown in Figure 1, this is an example of PDB ID 2PRT A to show sequence-specific and non-specific binding residues in the tertiary structure.

Finally, we discuss ligand binding sites in the tertiary structures of moonlighting proteins that are related to either of their primary or secondary functions.

The generation of the essential Fc tertiary conformation for binding to FcγRIIIa depends on the presence of the Fc oligosaccharides attached to the CH2 domains, and the antibody effector functions mediated via FcγRIIIa are severely abrogated in aglycosylated forms of antibodies (Tao and Morrison 1989; Krapp et al. 2003).

Tertiary structural analysis suggested the linear GRP78 primary amino acid sequence LIGRTWNDPSVQQDIKFL (Leu 98 -Leu(115)) as the putative binding site, containing the tertiary structuaLeu 98 -Leunt described above, which was confirmed experimentally.

Upon substrate binding, the tertiary structure of most proteins undergoes conformational changes that coordinate their function.

Because it is the MG-H1 moiety specifically that binds to the V domain, MG-H1-containing peptides or proteins, which have different secondary and tertiary structures, exhibit similar binding affinities and binding surfaces.

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