Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

9Z26

Cryo-EM structure of human TRPM4 channel in complex with calcium and NBA at 37 degrees Celsius (monomeric TMD-focused map with best-resolved NBA density)

This is a non-PDB format compatible entry.
Summary for 9Z26
Entry DOI10.2210/pdb9z26/pdb
EMDB information73764
DescriptorTransient receptor potential cation channel subfamily M member 4, CALCIUM ION, 4-chloranyl-2-(2-naphthalen-1-yloxyethanoylamino)benzoic acid (3 entities in total)
Functional Keywordsion channel, trp channel, membrane protein
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight134852.33
Authors
Jinhong, H.,Wei, L.,Juan, D. (deposition date: 2025-11-04, release date: 2026-06-10, Last modification date: 2026-07-01)
Primary citationHu, J.,Ievleva, S.,Park, S.J.,Lee, J.,Cheng, J.,O'Dea, G.,Sheng, J.,Du, J.,Lu, W.
Temperature and intrinsic Ca 2+ reshape TRPM4 pharmacology.
Nat.Struct.Mol.Biol., 33:973-984, 2026
Cited by
PubMed Abstract: Proteins operate in dynamic environments where ions, lipids and temperature collectively define their properties, yet most studies rely on simplified conditions that overlook these intrinsic variables. Here we show two such factors-temperature and Ca-remodel the function and pharmacology of TRPM4, an ion channel implicated in cardiac conduction, immune regulation, cancer and intestinal-fluid homeostasis. At physiological temperature and Ca, TPPO-previously considered a selective TRPM5 inhibitor inactive toward TRPM4-potently activates TRPM4, revealing strong synergy among temperature, Ca and ligand binding. By contrast, Necrocide-1, a necroptotic activator targeting the same binding pocket, defies this logic: it opens TRPM4 without Ca but is antagonized by Ca. Meanwhile, the inhibitors NBA and CBA engage a nearby pocket, locking the channel in a non-conductive pre-open state. Our findings highlight that even rigid binding pockets can exhibit temperature-dependent ligand recognition, revealing hidden pharmacology and informing selective, environment-aware therapeutic strategies.
PubMed: 42265346
DOI: 10.1038/s41594-026-01818-3
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.9 Å)
Structure validation

257179

PDB entries from 2026-07-29

PDB statisticsPDBj update infoContact PDBjnumon