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As in previous researches, docking is the crucial component in drug development.
Protein-protein docking is the prediction of the structure of the complex, given the structures of the individual proteins.
Computational docking is the core process of computer-aided drug design (CADD); it aims at predicting the best orientation and conformation of a small molecule (drug ligand) when bound to a target large receptor molecule (protein) in order to form a stable complex molecule.
Protein-protein docking is the computational prediction of protein complex structure given the individually solved component protein structures.
One of the critical parameters for ligand docking is the size of a search space used to identify low-energy binding poses of drug candidates.
Molecular docking is the most widely used method in modern computer-aided drug design, regardless of being used in virtual screen or lead optimization.
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Undocking and docking are the important stages of ASP flight which require the perfect automatic control.
The most important constraint in the cross-docking is the limited time for products storage inside the cross-dock (e.g., 24 h) (Schaffer 1998).
Even the dock is the same.
The key feature that sets this dock apart from other travel docks is the night light.
Just like the original Zeppelin, this speaker dock is the best in its class.
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