Membrane Transporter/Ion Channel


Membrane Transporters mediate the movement of ions and molecules via binding and moving the substance across the membrane. There are two main actions of transporter: facilitated diffusion (passive transport) and active transport. Membrane transporters which bind the hydrolysis of ATP to the transport of target molecules are referred to as ATPases. For instance, Na+,K+-ATPases or Na+,K+-pumps are responsible for the transport of Na+ out of and K+ into cells.
Ion channels are pore-forming membrane proteins which allow the flow of ions across the membrane. The ion channels can be broadly grouped into six families including calcium channels, chloride channels, potassium channels, sodium channels, gap junction proteins and porins. Not all ion channels are gated, such as certain type of K+ and Cl– channels, transient receptor potential superfamily of cation channels, the ryanodine receptors and the IP3 receptors, but most Na+, K+, Ca2+ and some Cl– channels are all gated by voltage. Ligand-gated channels are regulated in response to ligand binding (e.g. neurotransmitters signaling). These ligand-gated neurotransmitter receptors are known as ionotropic receptors. Various neurotransmitters couple to ionotropic receptors such as glutamate, acetylcholine, glycine, GABA, and serotonin.
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B7786 TRAM 39Summary: Potent KCa3.1 blocker -
B7789 Huwentoxin XVISummary: N-type Ca2+ channel blocker,potent and selective -
B4783 Diphenidol HClSummary: antagonist of muscarinic M2 and M3 receptor -
A8896 (+)-MK 801 MaleateSummary: Potent NMDA antagonist -
B4798 Procainamide HClTarget: DNA MethyltransferasesSummary: sodium channel blocker -
B4884 RBC8Summary: Ral GTPase inhibitor -
B4849 AzimilideSummary: class III anti-arrhythmic drug -
B4867 7ACC1Summary: MCT inhibitor -
B4868 7ACC2Summary: A potent MCT inhibitor -
B4926 ML 240Summary: ATP-competitive inhibitor of p97 ATPase

