glutamate receptor, ionotropic kainate 1; glutamate receptor 5; GluR-5; GluR5; excitatory amino acid receptor 3; EAA3 (GRIK1, GLUR5)
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Function
- non NMDA glutamate receptor subunit
- binding of the excitatory neurotransmitter L-glutamate induces a conformation change, leading to the opening of the cation channel, & thereby converts the chemical signal to an electrical impulse
- the receptor then desensitizes rapidly & enters a transient inactive state, characterized by the presence of bound agonist
- may be involved in the transmission of light information from the retina to the hypothalamus
- receptor binds domoate > kainate > L-glutamate = quisqualate > CNQX = DNQX > AMPA > dihydrokainate > NMDA
Structure
- homotetramer or heterotetramer of pore-forming glutamate receptor subunits
- tetramers may be formed by the dimerization of dimers (probable)
- belongs to the glutamate-gated ion channel (TC 1.A.10) family
Compartment
Alternative splicing
named isoforms=2 additional isoforms seem to exist
Expression
- most abundant in the cerebellum & the suprachiasmatic nuclei (SCN) of the hypothalamus
- expressed in motor neurons
Pathology
Genetics
- RNA editing:
- modified positions=636, partially edited
- the unedited version (Q) assembles into a functional kainate-gated homomeric channel, whereas the edited version (R) is unable to produce channel activity when expressed alone
- both edited & unedited versions can form functional channels with GRIK4 & GRIK5 (putative)
More general terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/P39086.html
- ↑ 2.0 2.1 Eubanks JH, Puranam RS, Kleckner NW, Bettler B, Heinemann SF, McNamara JO. The gene encoding the glutamate receptor subunit GluR5 is located on human chromosome 21q21.1-22.1 in the vicinity of the gene for familial amyotrophic lateral sclerosis. Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):178-82. PMID: https://www.ncbi.nlm.nih.gov/pubmed/8419920