Sentence examples for binding stable in the from inspiring English sources

For the MD simulation, the top three TCM compounds maintain most of interactions with Smo protein, which keep the ligand binding stable in the binding domain.

For the MD simulation, the top three TCM compounds maintain most of interactions with PXR protein, which keep the ligand binding stable in the binding domain.

Comparing to docking poses between docking simulation and MD simulation, LY2940680 and the top three TCM compounds maintain most of interactions with Smo protein, which keep the ligand binding stable in the binding domain.

After MD simulations, which can optimize the result of docking simulation and validate the stability of H-bonds between each ligand and Smo protein under dynamic conditions, top three TCM compounds maintain most of interactions with Smo protein, which keep the ligand binding stable in the binding domain.

After MD simulations, which can optimize the result of docking simulation and validate the stability of H-bonds between each ligand and PXR protein under dynamic conditions, top TCM compounds, BEMG and tangshenoside II, maintain most of interactions with PXR protein, which keep the ligand binding stable in the binding domain.

Reviewer 3: 1) The authors' data indicates that Ft-Ds binding is less stable in the absence of Fj.

Other than the concerns about less direct causes of the results, I had only a couple major comments: 1) The authors' data indicates that Ft-Ds binding is less stable in the absence of Fj.

The exact overlapping of these two images (Figure 3c) convinces that the QDs and AlPcSs are still bound together in cells, demonstrating that the electrostatic binding of AlPcS-QD is stable in the cellular environment.

Abacavir was found to be extremely stable in the binding pocket with minimal conformational changes (RMSD ≤ 0.5 Å); however, the observed RMSD of acyclovir ranged from 0.5 to 1.5 Å.

However, GABA was not stable in the binding pocket, and indeed, it completely exited the protein 4.6 ns into the equilibration.

Most other drugs that do not exhibit extremes of protein binding or lipophilicity remained relatively stable in the ex vivo ECMO circuit.