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Interestingly, gypsy elements, which harbor strong SU HW) binding sites, can boost transgene expression at many integration sites [51].
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Individual binding sites can be observed via the green FitCons2 class 40 (ρ = 0.43).
Changes during evolution to the DNA sequence in binding sites can lead to changes in gene expression.
These binding sites can be considered as prerequisite or allosteric binding sites.
Two RAP1 binding sites can substitute for the wild-type initiation site.
Some fluorescent probes have specific binding to different regions of the HSA, and the binding sites can be determined by the displacement binding experiments using some probes.
In addition, the electrostatic potential binding energy and similarity between the binding sites can be calculated based on the binding pose of the ligand.
Substantial similarity of EA receptors regarding their binding sites can be assumed.
However, the sequences of binding sites can be very heterogeneous.
The new binding site can be introduced with a minimum of four amino acid changes.
The value of n of BSA at all three studied temperatures is approximately equivalent to 1 as fractional binding sites don't occur and no < 1 binding site can be present suggesting only one binding site for rivaroxaban.
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