7PX8
CryoEM structure of mammalian acylaminoacyl-peptidase
Summary for 7PX8
| Entry DOI | 10.2210/pdb7px8/pdb |
| EMDB information | 13691 |
| Descriptor | Acylamino-acid-releasing enzyme (1 entity in total) |
| Functional Keywords | acylaminoacyl-peptidase, tetramer, aclypeptide-hydrolase, oxidized protein hydrolase, serine-protease, hydrolase |
| Biological source | Sus scrofa domesticus (domestic pig) |
| Total number of polymer chains | 4 |
| Total formula weight | 325297.56 |
| Authors | Kiss-Szeman, A.J.,Harmat, V.,Menyhard, D.K.,Straner, P.,Jakli, I.,Hosogi, N.,Perczel, A. (deposition date: 2021-10-08, release date: 2022-05-25, Last modification date: 2024-07-17) |
| Primary citation | Kiss-Szeman, A.J.,Straner, P.,Jakli, I.,Hosogi, N.,Harmat, V.,Menyhard, D.K.,Perczel, A. Cryo-EM structure of acylpeptide hydrolase reveals substrate selection by multimerization and a multi-state serine-protease triad. Chem Sci, 13:7132-7142, 2022 Cited by PubMed Abstract: The first structure of tetrameric mammalian acylaminoacyl peptidase, an enzyme that functions as an upstream regulator of the proteasome through the removal of terminal -acetylated residues from its protein substrates, was determined by cryo-EM and further elucidated by MD simulations. Self-association results in a toroid-shaped quaternary structure, guided by an amyloidogenic β-edge and unique inserts. With a Pro introduced into its central β-sheet, sufficient conformational freedom is awarded to the segment containing the catalytic Ser587 that the serine protease catalytic triad alternates between active and latent states. Active site flexibility suggests that the dual function of catalysis and substrate selection are fulfilled by a novel mechanism: substrate entrance is regulated by flexible loops creating a double-gated channel system, while binding of the substrate to the active site is required for stabilization of the catalytic apparatus - as a second filter before hydrolysis. The structure not only underlines that within the family of S9 proteases homo-multimerization acts as a crucial tool for substrate selection, but it will also allow drug design targeting of the ubiquitin-proteasome system. PubMed: 35799812DOI: 10.1039/d2sc02276a PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.27 Å) |
Structure validation
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