The four GO processes identified are GO 0003677 (DNA binding, molecular function), GO 0008270 (zinc ion binding, molecular function), GO 0046872 (metal ion binding, molecular function) and GO 0005634 (nucleus, cellular component).
As shown in Fig. 3A, using western blots, we identified strong crizotinib ALK binding in RU cells derived from SK-N-SH at 52 °C, at which no substantial crizotinib ALK binding was identified in RR cells.
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.
However, no binding media could be identified in our studies.
The DNA binding site of ArcR was identified in S. aureus SH1000, which is the same as the Fnr motif66.
The W-box is a binding motif that has been identified in WRKY transcription factors.
Three candidate ribosome receptors, p180, p34, and Sec61p, have been identified in binding studies with inactive ribosomes, suggesting that ribosome binding is mediated through a receptor-ligand interaction.
A frequently mutated novel gene, the nuclear receptor binding SET domain protein 1 (NSD1), was identified in 33 HNSCCs.
Candidate binding motifs similar to the Rap1p binding site and the stress-responsive element were identified in the promoter regions of differentially regulated genes.
Some critical amino acids are identified in ligand-binding sequence.
