7B05
TRPC4 in complex with inhibitor GFB-8749
Summary for 7B05
| Entry DOI | 10.2210/pdb7b05/pdb |
| EMDB information | 11957 4339 |
| Descriptor | Transient receptor potential cation channel subfamily c member 4a, 4-[4-[[4,4-bis(fluoranyl)cyclohexyl]methyl]-3-oxidanylidene-piperazin-1-yl]-5-chloranyl-1~{H}-pyridazin-6-one, CALCIUM ION, ... (4 entities in total) |
| Functional Keywords | ion channel, trpc4, inhibitor, complex, membrane protein, transport protein |
| Biological source | Danio rerio (Zebrafish) |
| Total number of polymer chains | 4 |
| Total formula weight | 423895.46 |
| Authors | Vinayagam, D.,Quentin, D.,Sistel, O.,Merino, F.,Stabrin, M.,Hofnagel, O.,Ledeboer, M.W.,Malojcic, G.,Raunser, S. (deposition date: 2020-11-18, release date: 2020-12-09, Last modification date: 2024-05-01) |
| Primary citation | Vinayagam, D.,Quentin, D.,Yu-Strzelczyk, J.,Sitsel, O.,Merino, F.,Stabrin, M.,Hofnagel, O.,Yu, M.,Ledeboer, M.W.,Nagel, G.,Malojcic, G.,Raunser, S. Structural basis of TRPC4 regulation by calmodulin and pharmacological agents. Elife, 9:-, 2020 Cited by PubMed Abstract: Canonical transient receptor potential channels (TRPC) are involved in receptor-operated and/or store-operated Ca signaling. Inhibition of TRPCs by small molecules was shown to be promising in treating renal diseases. In cells, the channels are regulated by calmodulin (CaM). Molecular details of both CaM and drug binding have remained elusive so far. Here, we report structures of TRPC4 in complex with three pyridazinone-based inhibitors and CaM. The structures reveal that all the inhibitors bind to the same cavity of the voltage-sensing-like domain and allow us to describe how structural changes from the ligand-binding site can be transmitted to the central ion-conducting pore of TRPC4. CaM binds to the rib helix of TRPC4, which results in the ordering of a previously disordered region, fixing the channel in its closed conformation. This represents a novel CaM-induced regulatory mechanism of canonical TRP channels. PubMed: 33236980DOI: 10.7554/eLife.60603 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.8 Å) |
Structure validation
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