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

7ZL3

Signal peptide mimicry primes Sec61 for client-selective inhibition

Summary for 7ZL3
Entry DOI10.2210/pdb7zl3/pdb
EMDB information14776 3068
DescriptorProtein transport protein Sec61 subunit alpha, Protein transport protein Sec61 subunit gamma, Protein transport protein Sec61 subunit beta, ... (4 entities in total)
Functional Keywordssec61 translocon, cryoem, membrane protein, protein biogenesis
Biological sourceOvis aries (sheep)
More
Total number of polymer chains4
Total formula weight63374.41
Authors
Rehan, S.,Paavilainen O, V. (deposition date: 2022-04-13, release date: 2023-03-22, Last modification date: 2023-11-15)
Primary citationRehan, S.,Tranter, D.,Sharp, P.P.,Craven, G.B.,Lowe, E.,Anderl, J.L.,Muchamuel, T.,Abrishami, V.,Kuivanen, S.,Wenzell, N.A.,Jennings, A.,Kalyanaraman, C.,Strandin, T.,Javanainen, M.,Vapalahti, O.,Jacobson, M.P.,McMinn, D.,Kirk, C.J.,Huiskonen, J.T.,Taunton, J.,Paavilainen, V.O.
Signal peptide mimicry primes Sec61 for client-selective inhibition.
Nat.Chem.Biol., 19:1054-1062, 2023
Cited by
PubMed Abstract: Preventing the biogenesis of disease-relevant proteins is an attractive therapeutic strategy, but attempts to target essential protein biogenesis factors have been hampered by excessive toxicity. Here we describe KZR-8445, a cyclic depsipeptide that targets the Sec61 translocon and selectively disrupts secretory and membrane protein biogenesis in a signal peptide-dependent manner. KZR-8445 potently inhibits the secretion of pro-inflammatory cytokines in primary immune cells and is highly efficacious in a mouse model of rheumatoid arthritis. A cryogenic electron microscopy structure reveals that KZR-8445 occupies the fully opened Se61 lateral gate and blocks access to the lumenal plug domain. KZR-8445 binding stabilizes the lateral gate helices in a manner that traps select signal peptides in the Sec61 channel and prevents their movement into the lipid bilayer. Our results establish a framework for the structure-guided discovery of novel therapeutics that selectively modulate Sec61-mediated protein biogenesis.
PubMed: 37169961
DOI: 10.1038/s41589-023-01326-1
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.2 Å)
Structure validation

247536

PDB entries from 2026-01-14

PDB statisticsPDBj update infoContact PDBjnumon