Muscarinic acetylcholine receptor M5

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

The human muscarinic acetylcholine receptor M5, encoded by the CHRM5 gene, is a member of the G protein-coupled receptor superfamily of integral membrane proteins. It is coupled to Gq protein.[5] Binding of the endogenous ligand acetylcholine to the M5 receptor triggers a number of cellular responses such as adenylate cyclase inhibition, phosphoinositide degradation, and potassium channel modulation. Muscarinic receptors mediate many of the effects of acetylcholine in the central and peripheral nervous system. The clinical implications of this receptor have not been fully explored; however, stimulation of this receptor is known to effectively decrease cyclic AMP levels and downregulate the activity of protein kinase A (PKA).

AliasesCHRM5, HM5, cholinergic receptor muscarinic 5
End34,067,458 bp[1]
Quick facts CHRM5, Identifiers ...
CHRM5
Identifiers
AliasesCHRM5, HM5, cholinergic receptor muscarinic 5
External IDsOMIM: 118496; MGI: 109248; HomoloGene: 22697; GeneCards: CHRM5; OMA:CHRM5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012125
NM_001320917

NM_205783

RefSeq (protein)

NP_001307846
NP_036257

NP_991352

Location (UCSC)Chr 15: 33.97 – 34.07 MbChr 2: 112.31 – 112.31 Mb
PubMed search[3][4]
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Ligands

No highly selective agonists or antagonists for the M5 receptor have been discovered as of 2018, but several non-selective muscarinic agonists and antagonists have significant affinity for M5.

The lack of selective M5 receptor ligands is one of the main reasons that the medical community has such a limited understanding of the M5 receptors effects as the possibility that any and/or all effects of non-selective ligands may be due to interactions with other receptors can not be ruled out. Some data may be obtained by observing which effects are common among semi-selective ligands (ex. a ligand of M1 and M5, a ligand of M2 and M5, and a ligand of M3 and M5), but until both a selective agonist and a selective antagonist of the M5 receptor are developed this data must be considered merely theoretical.

Agonists

Positive allosteric modulators

Negative allosteric modulators

Antagonists

See also

References

Further reading

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