https://www.selleckchem.com/pr....oducts/Naphazoline-h
Additionally, we identify the key residues located in antagonist ZM241385 binding pocket which mediate multiple allosteric pathways and have been experimentally proven to play a critical role in affecting the ligand potency. This study is helpful for understanding the allosteric communication mechanism of A2AAR, and can provide valuable information for the structure-based drug design of GPCRs. Communicated by Ramaswamy H. Sarma.Dynamic modifications of chromatin allow rapid access of the gene regulatory machine
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