Understanding the molecular basis of toxin promiscuity: the analgesic sea anemone peptide APETx2 interacts with ASIC3 and hERG channels via overlapping pharmacophores.
Understanding the molecular basis of toxin promiscuity: the analgesic sea anemone peptide APETx2 interacts with ASIC3 and hERG channels via overlapping pharmacophores.
Understanding the molecular basis of toxin promiscuity: the analgesic sea anemone peptide APETx2 interacts with ASIC3 and hERG channels via overlapping pharmacophores.
