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A number of preferred motifs were identified.
New structural motifs were identified, which combined sodium channel activity with decreased ADME liabilities.
Considering the principles of Watson Crick base pairing and the initial motif position, some motifs were identified as one type of SSR locus.
TNFR-associated factor (TRAF) 2-binding and TRAF3-binding motifs were identified in USP17, through which it interacted with and disrupted the TRAF2/TRAF3 complex.
Sixty-five motifsatellite motifs were identified, from which 38 functional STMS primer pairs were designed and validated.
Protein motifs were identified using MEME (http://meme.sdsc.edu/meme/intro.html).sdsc.edu/meme/intro.html
Using sequence alignment of the VMATs, VAChT and ecMdfA, several conserved residues and motifs were identified.
Three (3) distinctive log motifs were identified and correlated across other wells in the field of study.
Only two motifs were identified in both tissues (Figure 2B).
Four regulatory network motifs were identified from the interaction network.
Several common sequence motifs were identified among the selected 14 sequences (Fig S3).
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