Population
Human rhinovirus 14 and its drug-resistant mutants
Design
Preclinical
Authors
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Unifies rhinovirus antiviral mechanisms via shared VP1 pocket; leaves open potency determinants for therapeutic optimization.
Crystallographic analysis reveals that eight antiviral agents bind to the same hydrophobic pocket in human rhinovirus 14, inhibiting disassembly by reducing protein shell flexibility.
Badger et al. (1988) studied this question.
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