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  2. RAGE (receptor) - Wikipedia

    en.wikipedia.org/wiki/RAGE_(receptor)

    Schematic of the relation between an immunoglobulin and RAGE Schematic of the RAGE gene and its products. RAGE (receptor for advanced glycation endproducts), also called AGER, is a 35 kilodalton transmembrane receptor [5] of the immunoglobulin super family which was first characterized in 1992 by Neeper et al. [6] Its name comes from its ability to bind advanced glycation endproducts (), which ...

  3. Ligand-gated ion channel - Wikipedia

    en.wikipedia.org/wiki/Ligand-gated_ion_channel

    The name "NMDA receptor" is derived from the ligand N-methyl-D-aspartate (NMDA), which acts as a selective agonist at these receptors. When the NMDA receptor is activated by the binding of two co-agonists, the cation channel opens, allowing Na + and Ca 2+ to flow into the cell, in turn raising the cell's electric potential. Thus, the NMDA ...

  4. Receptor (biochemistry) - Wikipedia

    en.wikipedia.org/wiki/Receptor_(biochemistry)

    Partial agonists do not activate receptors with maximal efficacy, even with maximal binding, causing partial responses compared to those of full agonists (efficacy between 0 and 100%). Antagonists bind to receptors but do not activate them. This results in a receptor blockade, inhibiting the binding of agonists and inverse agonists.

  5. Cell surface receptor - Wikipedia

    en.wikipedia.org/wiki/Cell_surface_receptor

    Cell surface receptors (membrane receptors, transmembrane receptors) are receptors that are embedded in the plasma membrane of cells. [1] They act in cell signaling by receiving (binding to) extracellular molecules. They are specialized integral membrane proteins that allow communication between the cell and the extracellular space.

  6. Channel blocker - Wikipedia

    en.wikipedia.org/wiki/Channel_blocker

    The normal function of agonist binding is the generation of cellular changes leading to various downstream effects; these effects range from altering membrane potential to initiation of signaling cascades. [11] Conversely, when open channel blockers bind to the cell they prevent the normal function of agonist binding.

  7. Agonist - Wikipedia

    en.wikipedia.org/wiki/Agonist

    A co-agonist works with other co-agonists to produce the desired effect together. NMDA receptor activation requires the binding of both glutamate, glycine and D-serine co-agonists. Calcium can also act as a co-agonist at the IP3 receptor. A selective agonist is selective for a specific type of receptor. E.g.

  8. NMDA receptor - Wikipedia

    en.wikipedia.org/wiki/NMDA_receptor

    The agonist-binding module links to a membrane domain, which consists of three transmembrane segments and a re-entrant loop reminiscent of the selectivity filter of potassium channels. The membrane domain contributes residues to the channel pore and is responsible for the receptor's high-unitary conductance , high-calcium permeability, and ...

  9. Free fatty acid receptor 1 - Wikipedia

    en.wikipedia.org/wiki/Free_fatty_acid_receptor_1

    233081 Ensembl ENSG00000126266 ENSMUSG00000044453 UniProt O14842 Q76JU9 RefSeq (mRNA) NM_005303 NM_194057 RefSeq (protein) NP_005294 NP_918946 Location (UCSC) Chr 19: 35.35 – 35.35 Mb Chr 7: 30.56 – 30.56 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Free fatty acid receptor 1 (FFAR1), also known as G-protein coupled receptor 40 (GPR40), is a rhodopsin-like G-protein coupled ...