The phrase 'molecular docking techniques' is correct and can be used in written English.
It is used to describe computational techniques used to predict the binding of molecules to each other. For example: Scientists are using molecular docking techniques to better understand the interactions between molecules.
In this study a group of polyphenolic compounds was evaluated as potential inhibitors of arginine kinase using molecular docking techniques.
In this paper, the inhibitory kinetics of glabridin on tyrosinase and their binding mechanisms were determined using spectroscopic, zebrafish model and molecular docking techniques.
Further, the molecular mechanism underlying the inhibition of tyrosinse by amoxicillin was investigated by means of fluorescence quenching and molecular docking techniques.
Hence, the binding of harmine with sequence specific DNA oligonucleotides has been studied using various biophysical techniques i.e. absorption, fluorescence and molecular docking techniques.
DNA-binding study of 3f with sm-DNA was probed through UV vis absorption, fluorescence quenching, gel electrophoresis and molecular docking techniques.
The in vitro DNA binding studies of complex 1 with CT DNA was carried out by various biophysical and molecular docking techniques which revealed that complex 1 binds to DNA through intercalation in the minor groove having AT-rich sequences.
To explain the dual inhibition of MAO-B and AA2AR at the molecular level, molecular docking technique was employed.
Consequently, a molecular docking technique was run on a library of novel discontinuous peptides predicted by PEPOP from Human epidermal growth factor receptor 2 (HECD ECD) subdomain III.
The interactions of complexes 1 4 with human serum albumin (HSA) have been investigated in Tris HCl buffer solution at pH 7.4 by spectroscopic methods and a molecular docking technique.
The molecular docking technique was also utilized to ascertain the mechanism and mode of action of diphenyltin analog 3. The in vitro antitumor activity of 3 was evaluated by SRB assay against a panel of human cancer cell lines which clearly revealed good cytotoxic activity against K-562 human leukemic cells with GI50 values <10 μg/ml.
We present three interaction zones (zones vide −1 to −3) in the colchicine binding domain of Haemonchus contortus (a helminth) β-tubulin homology model and developed zone-wise structure-based pharmacophore models coupled with molecular docking technique to unveil the binding hypotheses.
