Sentence examples for binding potentially from inspiring English sources

Cbp binding potentially activates ligand localization for Csk kinase activity (Takeuchi et al., 2000; Wong et al., 2005).

APP copper binding potentially mitigates copper-induced PCa cell growth inhibition.

Firstly, fibre is thought to exert 'physical' effects such as increasing faecal bulk, hastening faecal transit and binding potentially co-carcinogenic bile salts.

However, the implications of this binding potentially extend beyond rituximab to any antibody-based therapeutic in RA, particularly those in which Fc-dependent function is important for clinical benefit.

Based on these results, we predicted that the extracellular addition of CSPG4-N30-640 proteins might compete with the full-length CSPG4 protein for TcdB binding, potentially resulting in an inhibitory effect.

In contrast to the two AAA+ ATPases that are present in many different multisubunit complexes (RUVBL1 and RUVBL2), PIH1D1 and RPAP3 are specific to the R2TP complex and are likely to define substrate binding, potentially via interaction with the tetratricopeptide repeats of RPAP3.

Dosage imbalance involves changes in protein concentrations relative to those of potential binding partners, potentially resulting in improper protein complex assembly (Veitia 2002), spurious interactions (Liberles et al. 2011), and deleterious downstream effects on pathways.

The antibody library described here allows the isolation of new stable binding specificities, potentially exploitable as immunochemical reagents for intracellular applications.

Although classical approaches to G-protein-coupled receptor (GPCR) drug design have targeted the orthosteric binding site, potentially all GPCRs possess druggable allosteric sites.

We illustrate this point by discussing the derivation of fractal exponents describing protein water interactions, and their application to protein roughness, protein binding and potentially protein engineering.

For the first time, several residues of the C-terminus previously proposed to be involved in subtype selectivity are resolved and three of them extend into the ligand binding site potentially allowing for selective drug design.