9PCX
22bin20S complex (NSF-alphaSNAP-2:2 syntaxin-1a:SNAP-25), hydrolyzing, class 14
Summary for 9PCX
| Entry DOI | 10.2210/pdb9pcx/pdb |
| Related | 9OJ2 9OJJ 9OJR 9OJU 9OJZ 9OK3 9OK5 9OKC 9OLJ 9OLO 9OM6 9OMQ 9PAF 9PAG 9PB9 9PBA 9PBF 9PBV 9PC3 |
| EMDB information | 71521 |
| Descriptor | Vesicle-fusing ATPase, Syntaxin-1A, Synaptosomal-associated protein 25,Synaptosomal-associated protein 25, Alpha-soluble NSF attachment protein chimera, ... (6 entities in total) |
| Functional Keywords | atpase, snare, hydrolysis, disassembly, translocation, exocytosis, neurotransmitter release, synapse, synaptic transmission, membrane fusion, hydrolase |
| Biological source | Cricetulus griseus (Chinese hamster) More |
| Total number of polymer chains | 14 |
| Total formula weight | 915173.66 |
| Authors | White, K.I.,Brunger, A.T. (deposition date: 2025-06-29, release date: 2025-08-06, Last modification date: 2025-10-08) |
| Primary citation | White, K.I.,Khan, Y.A.,Qiu, K.,Balaji, A.,Couoh-Cardel, S.,Esquivies, L.,Pfuetzner, R.A.,Diao, J.,Brunger, A.T. Structural remodeling of target-SNARE protein complexes by NSF enables synaptic transmission. Nat Commun, 16:8371-8371, 2025 Cited by PubMed Abstract: Synaptic vesicles containing neurotransmitters fuse with the plasma membrane upon the arrival of an action potential at the active zone. Multiple proteins organize trans-SNARE complex assembly and priming, leading to fusion. One target membrane SNARE, syntaxin, forms nanodomains at the active zone, and another, SNAP-25, enters non-fusogenic complexes with it. Here, we reveal mechanistic details of AAA+ protein NSF (N-ethylmaleimide sensitive factor) and SNAP (soluble NSF attachment protein) action before fusion. We show that syntaxin clusters are conserved, that NSF colocalizes with them, and characterize SNARE populations that may exist within or near them using cryo-EM. Supercomplexes of NSF, α-SNAP, and either a syntaxin tetramer or one of two binary complexes of syntaxin-SNAP-25 reveal atomic details of SNARE processing and show how sequential ATP hydrolysis drives disassembly. These results suggest a functional role for syntaxin clusters as reservoirs and a corresponding role for NSF in syntaxin liberation and SNARE protein quality control preceding fusion. PubMed: 40993127DOI: 10.1038/s41467-025-62764-0 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (4.03 Å) |
Structure validation
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