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Specificity of binding can be shown in terms of reproducibility of the docked conformation of the compounds.
Similar(58)
Since the T molecule hinders starch degradation by binding to M molecules and preventing them from binding to S, it can be shown that this model can also implement arithmetic division between the S and T molecule concentrations.
Moreover, we show that both PrPc and PrPsc bind RADA and binding can be competitively inhibited with Congo red.
It was previously shown that specific binding can be adequately modeled as a combination of selection for the native ligand and against a single non-specific decoy ligand [ 14].
Previous work showed that Dichaete binding can be detected at the midline enhancer with specific PCR assays despite an apparent lack of binding in BDTNP and modENCODE datasets [ 21, 25] and we note that a low stringency DamID peak overlaps the GMR32A06 regulatory region encompassing the sli midline enhancer.
Ligand binding can be divided into specific and nonspecific binding.
The ion binding motifs are shown.
Intermediate bindings between two substructures are shown.
Similar expansions of retrotransposons that carry CTCF binding might, in fact, have an evolutionary advantage over those that do not: it has been shown that CTCF binding can prevent DNA methylation and the establishment of repressive chromatin modifications (Lee et al., 2010; Rand et al., 2004).
It has been shown that GAGs can alter the binding with selectins because the latter bind several glycoproteins [ 53].
It has been shown that virus binding to infected cells can occur up to 24 hpi [ 10].
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