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Glycopeptides 4 and 7 are Aq-specific, i.e. they both displayed affinity for Aq but bound poorly to DR4.
Several of these domains, including DBL5ε, have, to some extent, displayed affinity for CSA in vitro [12], [13], [14], [15] [16].
With the exception of compounds 4, 5 and 10, all compounds displayed affinity for the α1-ARs in the micromolar range (Table 1).
PaLPMO9H displayed affinity for non-cellulosic substrates including XG, β-glucans, and glucomannan.
Similar(56)
Herpes simplex viruses (HSVs) display affinity for cell-surface heparan sulfate proteoglycans with biological relevance in virus entry.
In contrast, we have no clear-cut explanation for the decreases in diastolic blood pressure induced by rauwolscine, which does not display affinity for α1-adrenoceptors.
Dihydroergotamine (DHE) is an acute antimigraine agent that displays affinity for dopamine D2-like receptors, serotonin 5-HT1/2 receptors and α1/α2-adrenoceptors.
Over the years, a large number of compounds with unrelated chemical structures have been reported to display affinity for σ receptors (Fig. 1).
PHD domains in other proteins also display affinity for methylated histones, such as PHF8, which binds to H3K4-me3 in rDNA [57].
In the large 14-3-3-phosphoproteomics 14-3-3-phosphoproteomics 14-3-3-phosphoproteomics 14-3-3-phosphoproteomicsinity for binding to 14-3-3 [ 1– 13].
The AhR gene also displays affinity for structurally related xenobiotics, including polychlorinated dibenzo- p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and coplanar polychlorinated biphenyls (PCBs) (Denison et al. 2002).
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