Sentence examples for binding are positioned in from inspiring English sources

Exact(1)

Although the folds of the dimer half-sites between the P. fluorescens LapDOutput and CdgS9Output are almost identical (rmsd of 1.9 Å) and the conserved GWxQ motifs, which are important for LapG binding, are positioned in identical, surface-exposed loops within each half-site, the dimer topology of the two output domain ortholog structures is substantially different.

Similar(59)

Critical residues involved in netrin-1 binding are positioned on either side of this structural feature, shown as site 1 and 2, respectively.

Thus, it was interesting to determine how candidate human-specific TF-binding sites are positioned in the genome relative to the genomic coordinates of these 24 genes.

Typically, TTR inhibitors and T4 bind in what is referred to as the forward binding mode, where anionic substituents like carboxylate are positioned in the outer binding pocket engaging in electrostatic interaction with the Lys15 ε-ammonium groups.

Gab4 contains the 14-3-3 14-3-3 14-3-3 around S210, bindingks the motif around T391 and the typical Grb2 binding S210, which is positioned in N-terminal vicinity of T391.

We manually selected the primer-binding sites to be positioned in regions where the sequences were highly similar between zebra finch and chicken and attempted to include as few degenerate bases as possible, but most primers (encompassing 18 pairs) required the inclusion of degenerate bases.

However, the GABAC receptor is unusual in that there are no tryptophan residues in the binding pocket; where Trp is positioned in related nACh, 5-HT3 and MOD-1 receptor binding sites, it has been replaced by Tyr in the GABAC receptor.

To identify the PIP2-binding sites, Kir channels were positioned in a preformed bilayer in orientations defined by self-assembly simulations (29) (see the Supporting Information for details).

As Thr is located within the CaM-binding region and Ser is positioned in the C-terminal tail, we propose that the AIE enables eNOS regulation through the modulation of eNOS phosphorylation at Thr and Ser.

The D1-selective and potent agonist doxanthrine was positioned in the binding site during construction.

The selective and potent D2 receptor agonist - R -2-OH-NPA was positioned in the binding site during the construction of the receptor model and thereby induced a conformational change of the receptor, where the binding site is shaped to accommodate an agonist.

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