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The binding site is viewed and represented as in Figure 4, omitting the electron-density map.
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We propose that the peak detection for each of the binding sites be viewed as a scoring system on the set of all possible binding site regions.
We propose that the peak detection for each of the binding sites be viewed as a scoring system on sets of all possible SUMO binding site regions, and the UCSC TFBS data set be viewed as known TFBS regions when annotating the SUMO binding site regions.
Continuous binding of transcriptional activators to their cognate promoter binding sites is generally viewed as being necessary for ongoing transcription (Ho et al. 1996).
Otherwise, this binding site is regarded as an incorrectly predicted binding site.
The occurrence of the Gal binding site is apparently independent from the binding profiles of GI NoVs.
The binding site is very highly conserved.
If the genes that do have a particular binding site are over-represented in the group, this is viewed [31] as indicative of functionality of the corresponding BSs.
Atomic distances between corresponding binding residues within each binding site were measured in Deep View.
The lower binding site was found more constructive favorable for binding.
The dexamethasone binding site was the primary binding site in the GR for all organotins.
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