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Selective binding was found for radio-labelled palmitate which binds to BSA and β-lg but not to α-la (Perez et al. 1993).
Minimal to no binding was found for the FITC-Ahx-GGGAGGGA control peptide.
Notably no binding was found for BAY 58-2667 (1) thethe catalytic domain.
Regardless of the collagenous structure immobilized, only weak binding was found for actMMP-9 (not shown) and for actMMP-2.
A relatively high value of Δ G u 0 = −9.5 kcal/mol, indicative of tight binding was found for ghrelin.
Similar(55)
No marked differences in binding were found for 125I-Cry1Ac between resistant and susceptible strains (Fig. 3B).
Non-specific binding was found to account for <1% of total binding.
Instead, combinatorial binding was found to be significant for genetic and evolutionary stability; cobound TFs tend to disappear in concert and were sensitive to genetic knockout of partner TFs.
For the two cell lines tested (V79 Chinese hamster fibroblasts and 9L rat glioma), the oxygen dependence of binding was found to be the same for the two techniques.
A previously predicted ligand-binding motif of MARCO [ 19] was not found in the SRCR domains of SRAI and SCARA5; however, the lysine-rich region in the collagenous domain of SRAI hypothesized to be necessary for ligand binding was found in all other cA-SRs.
Ligand interactions with hPR B showed lower binding affinity than with hPR A. A similar pattern of binding affinity was found for ligands with hPR B, except for progesterone and cholesterol.
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