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The results of applying this analysis to the DNA binding interactions of both minor groove drugs and intercalators are discussed.
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These results supported the previous report that the binding interactions of p53 to both MDM2 and MDMX were very similar [26], [27].
Here, we exhaustively assess the atomistic binding interactions of this compound with both CCR5 and CXCR4, and we find that binding is driven by π-stacking interactions between aromatic rings on the ligand and receptor residues, as well as electrostatic interactions involving the protonated piperidine nitrogen.
These cryo-EM maps provided the first view on the conformation and binding interactions of an aa-tRNA with both EF-Tu and the ribosome.
Interestingly, these studies also identified unanticipated binding interactions of well-known drugs with alternative targets.
Collectively, the progress has reduced the binding interactions of brackets and established constant force systems.
The binding interactions of compounds with high binding affinity to Bcl-2 protein were analyzed.
The copolymers were designed to take advantage of the well-established binding interactions of calixarenes with neutral molecules and ions.
The binding interactions of the active compound with lysozyme were explored using multiple spectroscopic studies.
Furthermore, the binding interactions of compound 7k with α-glucosidase was confirmed through molecular docking.
Here, we have characterized the binding interactions of pSXXF tetrapeptides using NMR spectroscopy and calorimetry.
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