Membrane Transporter/Ion Channel
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.
- B7770 Agitoxin 2Summary: Shaker K+ channel blocker, potent
- B5037 CamstatinSummary: analog of PEP-19 with antagonism of calmodulin
- B5048 ω-Conotoxin GVIASummary: blocker of N-type calcium channels
- B5054 PicrotoxinSummary: GABAA receptor antagonist
- B5090 Tertiapin-QSummary: high affinity blocker for inward-rectifier K+ channels
- B5092 RyanodineSummary: Potent inhibitor of Ca2+ release from sarcoplasmic reticulum
- B5134 L-R4W2Summary: Vanilloid TRPV1 (VR1) receptor antagonist peptide
- B5143 Pep1-TGLSummary: Peptide containing the 'TGL' motif that corresponds to the C-terminus of GluR1 subunit
- B5144 Pep1-AGLSummary: Analog of Pep1-TGL
- B5165 Ionomycin calcium saltSummary: ionophore