In humans, molecular modelling and docking experiments have shown that
putrescine fits into the binding pocket of the human
TAAR6 and TAAR8 receptors.[9]
G protein-coupled receptors (GPCRs, or GPRs) contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins, supplied by
OMIM[7]
† References for all endogenous human TAAR1 ligands are provided at
List of trace amines
‡ References for synthetic TAAR1 agonists can be found at
TAAR1 or in the associated compound articles. For TAAR2 and TAAR5 agonists and inverse agonists, see
TAAR for references.
In humans, molecular modelling and docking experiments have shown that
putrescine fits into the binding pocket of the human
TAAR6 and TAAR8 receptors.[9]
G protein-coupled receptors (GPCRs, or GPRs) contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins, supplied by
OMIM[7]
† References for all endogenous human TAAR1 ligands are provided at
List of trace amines
‡ References for synthetic TAAR1 agonists can be found at
TAAR1 or in the associated compound articles. For TAAR2 and TAAR5 agonists and inverse agonists, see
TAAR for references.