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

9BW6

Human Vault Cage in complex with PARP4

Summary for 9BW6
Entry DOI10.2210/pdb9bw6/pdb
EMDB information44955
DescriptorMajor vault protein, Protein mono-ADP-ribosyltransferase PARP4 (2 entities in total)
Functional Keywordsvault, vault cage, mvp, major vault protein, spfh, parp4, poly(adp-ribose)polymerase 4, mint, poly(adp-ribose)polymerase, ribonucleoprotein, megadalton complex, tep1, vault rna, protein transport
Biological sourceHomo sapiens (human)
More
Total number of polymer chains4
Total formula weight584525.88
Authors
Lodwick, J.E.,Zhao, M. (deposition date: 2024-05-20, release date: 2025-02-05)
Primary citationLodwick, J.E.,Shen, R.,Erramilli, S.,Xie, Y.,Roganowicz, K.,Kossiakoff, A.A.,Zhao, M.
Structural Insights into the Roles of PARP4 and NAD + in the Human Vault Cage.
Biorxiv, 2024
Cited by
PubMed Abstract: Vault is a massive ribonucleoprotein complex found across Eukaryota. The major vault protein (MVP) oligomerizes into an ovular cage, which contains several minor vault components (MVCs) and is thought to transport transiently bound "cargo" molecules. Vertebrate vaults house a poly (ADP-ribose) polymerase (known as PARP4 in humans), which is the only MVC with known enzymatic activity. Despite being discovered decades ago, the molecular basis for PARP4's interaction with MVP remains unclear. In this study, we determined the structure of the human vault cage in complex with PARP4 and its enzymatic substrate NAD . The structures reveal atomic-level details of the protein-binding interface, as well as unexpected NAD -binding pockets within the interior of the vault cage. In addition, proteomics data show that human vaults purified from wild-type and PARP4-depleted cells interact with distinct subsets of proteins. Our results thereby support a model in which PARP4's specific incorporation into the vault cage helps to regulate vault's selection of cargo and its subcellular localization. Further, PARP4's proximity to MVP's NAD -binding sites could support its enzymatic function within the vault.
PubMed: 38979142
DOI: 10.1101/2024.06.27.601040
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.9 Å)
Structure validation

231564

PDB entries from 2025-02-19

PDB statisticsPDBj update infoContact PDBjnumon