Sentence examples for binding targets are often from inspiring English sources

Although purified compounds from these natural products present good therapeutic activities, molecular mechanisms of action including the identification of binding targets are often shrouded in mystery.

In general, the binding sites of the traditional targets are often concave pockets; in contrast, the surfaces of amyloid fibers are flat and repetitive along the fiber axis, without well-defined surface cavities.

Their targets are often restructured as partnerships.

Hence, the parts of a query molecule that are important for binding to the protein target are often unknown.

External targets were often cited as barriers.

The fragment-linking approach of SAR by NMR seems particularly well suited to targeting PPIs whose binding sites are often formed by distinct, adjacent subpockets.

However, the decisions of these bodies are not binding and are often ignored.

When a drug binding to the target is introduced into the system, changes in the target level are often modeled dynamically using modifications of an enzyme turnover model.

Direct targets of metals are often metalloproteins and metal binding molecules like chlorophyll (Küpper et al. 1996).

Drug discovery for difficult targets that have large and flat binding sites is often better suited to compounds beyond the "rule of 5" (bRo5).

The design of such protein binding molecules is often based on an antibody against the target protein, or involves the generation of smaller molecules that retain the binding characteristics of the antibody.