9BW6
Human Vault Cage in complex with PARP4
Summary for 9BW6
Entry DOI | 10.2210/pdb9bw6/pdb |
EMDB information | 44955 |
Descriptor | Major vault protein, Protein mono-ADP-ribosyltransferase PARP4 (2 entities in total) |
Functional Keywords | vault, 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 source | Homo sapiens (human) More |
Total number of polymer chains | 4 |
Total formula weight | 584525.88 |
Authors | |
Primary citation | Lodwick, 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: 38979142DOI: 10.1101/2024.06.27.601040 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.9 Å) |
Structure validation
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