Sentence examples for binding of these compounds from inspiring English sources

However, the structural effects of the binding of these compounds with the enzyme active site are not completely understood.

Furthermore, the CoMFA model was able to accurately predict the binding of these compounds to the neuronal sodium channel.

Amino acid residues of binding site namely; Lys255, Ser256, Leu258 and Asn265 are involved in binding of these compounds.

A possible mechanism of interaction implicating binding of these compounds to β-hematin was supported by in vitro tests.

We found different binding sites namely catalytic, inhibitory phosphorylation, cyclin binding and CKS-binding site of the CDK2 contributing towards the binding of these compounds.

Nuclear magnetic resonance (NMR) suggested direct binding of these compounds to the receptors pre-complexed with estradiol and further demonstrated that no estradiol displacement occurred.

This finding may indicate the essential structural factors for binding to TR, although binding affinities of these compounds might be much lower than those of the endogenous ligands T3 and T4.

CLK1 co crystal structures with two inhibitors revealed the binding mode of these compounds within the ATP-binding pocket.

The κ opioid receptor binding ability of these compounds were evaluated with opioid receptors binding assays.

Comparing the docked poses with the binding modes of these compounds confirmed that they were placed correctly in the binding site in at least one kinase of the docking panel (RMSD of maximum common substructure <2 Å).

The GOLD-predicted binding modes of these compounds were analysed, revealing close similarity to the UNITY-predicted binding modes.