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The cognate binding sites were aggregated from phylogenetically distinct targets (different CATH H-levels).
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Potential binding sites were elucidated by docking.
Ligand binding sites were predicted using 3DLigandSite.
Two binding sites were identified for GF.
Further, the use of these techniques along with others like elemental analysis or size distribution analysis allowed the identification of functional supramolecular aggregates in HS in which these binding sites are distributed [19].
Here, these binding sites are not discussed one by one.
One method to reduce the presence of these information-poor binding sites is to apply stricter binding site conservation criteria.
These binding sites are highly charged.
Noteworthy, these binding sites are juxtaposed to GATA3-binding sites.
No PHA-L-binding sites were observed.
Otherwise, this binding site is regarded as an incorrectly predicted binding site.
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binding sites were selected
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binding sites were shared
binding sites were identified
binding sites were used
binding sites were shown
binding sites were overrepresented
binding sites were associated
binding sites were generated
binding sites were revealed
binding sites were designed
binding sites were performed
binding sites were mapped
binding sites were extracted
binding sites were visualized
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