Mu Opioid Receptor: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
Michal Harel (talk | contribs) No edit summary |
||
| Line 2: | Line 2: | ||
<StructureSection load='4n6h' size='340' side='right' caption='Chimera of human Delta Opioid 7TM Receptor and E. coli cytochrome B562 in complex with oleate, tartrate, naltrindole, oleate derivative and Na+ ion (PDB code [[4n6h]])' scene=''> | <StructureSection load='4n6h' size='340' side='right' caption='Chimera of human Delta Opioid 7TM Receptor and E. coli cytochrome B562 in complex with oleate, tartrate, naltrindole, oleate derivative and Na+ ion (PDB code [[4n6h]])' scene=''> | ||
Opioid receptors are G-protein coupled receptors (GPCR), which bind endogenous opioid peptide neurotransmitters (such as enkephalins and endorphins) and exogenous synthetic opiate drugs (such as morphine, codeine, and heroin) as ligands to hinder pain-signaling in the brain, peripheral nerves, and digestive tract. μ-opioid receptors are one of the four major classes of opioid receptors, which also includes δ-opioid receptors, κ-opioid receptors, and nociceptin opioid receptors. The '''μ-opioid receptor''' MOR-1 is expressed by the gene OPRM1 in vertebrates. <ref name="past">DOI: 10.1124/pr.112.007138</ref> MOR-1 has important implications as a target for pain relievers as well as a treatment for drug abuse. | Opioid receptors are G-protein coupled receptors (GPCR), which bind endogenous opioid peptide neurotransmitters (such as enkephalins and endorphins) and exogenous synthetic opiate drugs (such as morphine, codeine, and heroin) as ligands to hinder pain-signaling in the brain, peripheral nerves, and digestive tract. μ-opioid receptors are one of the four major classes of opioid receptors, which also includes δ-opioid receptors, κ-opioid receptors, and nociceptin opioid receptors. The '''μ-opioid receptor''' MOR-1 is expressed by the gene OPRM1 in vertebrates. <ref name="past">DOI: 10.1124/pr.112.007138</ref> MOR-1 has important implications as a target for pain relievers as well as a treatment for drug abuse. | ||
See also [[Transmembrane (cell surface) receptors]] | |||
== Structural highlights == | == Structural highlights == | ||