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C.R.R. performed the molecular docking experiments.
Docking experiments support these results.
Docking experiments suggest the dimer interface as a possible location.
Docking experiments were performed at various exhaustiveness values of the default, 16, 24, 32, 40 and 60.
Ligand docking experiments were employed to gain information about residues involved in proline binding.
The anticipated binding mode of these analogs was confirmed by performing the in silico docking experiments.
Docking experiments on PTR1 identified preferential binding interactions and docking scores.
Molecular docking experiments showed 11b to possess rational binding modes to both the enzymes.
The molecular features that govern their bioactivity were explored through in silico docking experiments.
Docking experiments were carried out to identify the EID-1 binding surface on SHP structure.
The binding modes between chromenylchalcone 11 and aurora kinases were elucidated using in silico docking experiments.
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