Sentence examples for interactions are located from inspiring English sources

In our study, 14% of the interactions are located in the alternative splicing sites.

Thus, the determinants for formation of the cooperative side-chain interactions are located mainly in the α-helical domain.

These regions of interactions are located at the N- and C-terminal parts of both molecules and explain why we could detect expression of a fragment corresponding to the size of a Jmjd6-YFP dimer only in cells transfected with the full-length Jmjd6- F1/R5 -YFP fusion construct (Figure 6).

The interactions are located in highly conserved regions for all examples of which we are aware.

Figure  3B and C shows that the most prevalent interactions are located around the catalytic center.

The binding properties and specificities of the adhesive interactions are located in the N-terminal segment of the molecules.

Four of the SNPs identified in these interactions were located in two pathways well known to impact depression: neurotransmitter (ANKK1 and DRD2) and neuroendocrine (GNRH1 and ACVR2B) signalling.

As expected, most of the hydrogen bond donors belonged to residues involved in helix formation, but several hydrogen bond interactions were located in the loop region, including the amide hydrogens of Gly17, Gly18, and Ile20.

The results suggest that examining G × G interactions improves the identification of genetic associations predictive of depression. 4 of the SNPs identified in these interactions were located in two pathways well known to impact depression: neurotransmitter (ANKK1 and DRD2) and neuroendocrine (GNRH1 and ACVR2B) signalling.

Three point mutations in vac14-2 that impair protein interaction are located in predicted intrarepeat loops, R61K and H56Y in HEAT 2 and Q101R in HEAT 3. The location in the intrarepeat loops of three, random independent mutations that alter protein interactions supports the prediction of the HEAT repeat structure of Vac14.

Furthermore, a polypeptide corresponding to the sequence following the NPTH cleavage site also interacted with HrpB2 indicating that the site for interaction is located after the NPTH site.