The binding sites would not only reveal mRNA targets but would show GQ motif consensus if that's really the in vivo binding site for Aven.
A protein binding site would be an attractive hypothesis.
A defined consensus sequence for the AtoC binding site would greatly facilitate the identification of potential AtoC binding elements.
Using the same amplifying strategy as before the H2-binding site would also be present offering a second binding site.
Furthermore, the proximity of two phenolic oxygen atoms from each TBC[4] fragment would present additional binding sites for metal ions.
In this contribution, improved and accelerated methods for the comparison of protein binding sites are presented.
The higher geometric mean ratios and apparent lower plasma exposure of SU012662 could potentially have been related to low-capacity tight/target tissue binding sites, which would be only present after the first dose at very low concentrations with limited sampling.
Thus, it is reasonable to suggest that cNTnC·Ca2+·cTnI144−163 would present a more stable complex with a higher-affinity binding site for drug compounds than cNTnC·Ca2+·cTnI147−163.
Twelve binding sites are present within the dodecameric channel.
Multiple E-box binding sites are present within the −2 kb promoter regions.
