Sentence examples for direction of binding from inspiring English sources

We show that NES peptides can bind the CRM1 groove bidirectionally (in both plus and minus directions), and biochemical and structural analyses identified determinants for one direction of binding vs the other.

Take your chosen fabric and wrap it around the front and back of your journal(in the opposite direction of the binding).

The Fermi Edge is around zero point due to the charge effect, and the Cut-off Edge is shifted to the direction of high binding energy which indicates the decrease of the TiN work function with increasing HfO2 thickness from Fig. 5(a).

The largest enzyme classes tend to be oxidoreductases or subunits of oxidoreductases, and the relationships among members of these groups point in the direction of shared binding capacities accounting for the sequence relatedness, e.g. Fe-S clusters.

Candidate DBRs with an FDR corrected P-value of < 0.01 were called as differentially enriched between castes, and the direction of differential binding enrichment was determined from the MAnorm-produced normalized between-comparison ChIP enrichment M-value (log2 ratio).

When the sequence and the hydrophobic spacing pattern of an NES are reversed, the direction of the peptide binding CRM1 is also reversed.

Inside-out signaling induces a conformational change from the cytoplasmic domains in the direction of the extracellular binding site, in response to intracellular signaling events.

This analysis suggests the same rate-limiting transition state is being followed in the forward and reverse directions for binding and dissociation of nonspecific DNA (i.e., two-state behavior).

Previous reports on melanophore transport in Xenopus melanosomes showed that dynactin serves as an activator of kinesin-2 via direct binding of p150Glued to KAP3 and regulates the intracellular direction of melanosome transport by binding to either dynein (retrograde) or KAP3 (anterograde) (36).

Compared to non-specific adsorption, specific adsorption often orients the enzyme molecule in a direction allowed by the nature of binding and the spatial complementary effect which may contribute for the higher activity in glutaraldehyde-activated microreactors.

At these physiological metal concentrations, the concentration of Mn+2 is not large enough to shift the equilibrium of binding in the direction of metal-phosphate complex formation.