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Open data
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Basic information
| Entry | Database: PDB / ID: 9ny4 | ||||||
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| Title | USP21 bound to H2AK119ub nucleosome | ||||||
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Keywords | NUCLEAR PROTEIN / Deubiquitinase / DNA-binding protein / DNA | ||||||
| Function / homology | Function and homology informationdeNEDDylase activity / TNFR1-induced proapoptotic signaling / protein deubiquitination / cysteine-type peptidase activity / transcription initiation-coupled chromatin remodeling / TNFR1-induced NF-kappa-B signaling pathway / Regulation of TNFR1 signaling / structural constituent of chromatin / nucleosome / heterochromatin formation ...deNEDDylase activity / TNFR1-induced proapoptotic signaling / protein deubiquitination / cysteine-type peptidase activity / transcription initiation-coupled chromatin remodeling / TNFR1-induced NF-kappa-B signaling pathway / Regulation of TNFR1 signaling / structural constituent of chromatin / nucleosome / heterochromatin formation / nucleosome assembly / ubiquitinyl hydrolase 1 / cysteine-type deubiquitinase activity / transcription coactivator activity / Ub-specific processing proteases / protein heterodimerization activity / proteolysis / DNA binding / nucleoplasm / metal ion binding / nucleus / plasma membrane / cytosol / cytoplasm Similarity search - Function | ||||||
| Biological species | synthetic construct (others) Homo sapiens (human) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.98 Å | ||||||
Authors | Rahman, S. / Wolberger, C. | ||||||
| Funding support | United States, 1items
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Citation | Journal: Sci Adv / Year: 2025Title: Mechanism of USP21 autoinhibition and histone H2AK119 deubiquitination. Authors: Sanim Rahman / Chad W Hicks / Alexander Gwizdala / Cynthia Wolberger / ![]() Abstract: Monoubiquitinated histone H2A lysine 119 (H2AK119ub) is a modification associated with transcriptional silencing and heterochromatin formation. Ubiquitin-specific protease 21 (USP21), one of four ...Monoubiquitinated histone H2A lysine 119 (H2AK119ub) is a modification associated with transcriptional silencing and heterochromatin formation. Ubiquitin-specific protease 21 (USP21), one of four major H2AK119-specific deubiquitinating enzymes (DUBs), plays critical roles in diverse cellular processes. However, the mechanisms by which USP21 specifically deubiquitinates H2AK119ub and is regulated are unknown. We determined the cryo-EM structure of the USP21 catalytic domain bound to an H2AK119ub nucleosome, which revealed a recognition mode that differs from that of other H2AK119-specific DUBs. We unexpectedly found that the N-terminal IDR of USP21 inhibits the enzyme's activity. Using AlphaFold-Multimer to perform a virtual screen of USP21 interactors, we identified kinases that phosphorylate the USP21 IDR and thereby relieve autoinhibition. AlphaFold3 modeling of USP21 suggests a structural model for autoinhibition. AlphaFold analysis suggests that phosphorylation-regulated autoinhibition may be a feature of various USP enzymes. These findings shed light on the mechanisms of H2AK119 deubiquitination and reveal a previously unexplored mode of phosphorylation-dependent DUB autoregulation. | ||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9ny4.cif.gz | 357.3 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9ny4.ent.gz | 266.9 KB | Display | PDB format |
| PDBx/mmJSON format | 9ny4.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9ny4_validation.pdf.gz | 1.4 MB | Display | wwPDB validaton report |
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| Full document | 9ny4_full_validation.pdf.gz | 1.4 MB | Display | |
| Data in XML | 9ny4_validation.xml.gz | 47.1 KB | Display | |
| Data in CIF | 9ny4_validation.cif.gz | 75.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ny/9ny4 ftp://data.pdbj.org/pub/pdb/validation_reports/ny/9ny4 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 49919MC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-Protein , 6 types, 10 molecules AEBFCGDHKU
| #1: Protein | Mass: 15435.126 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() #2: Protein | Mass: 11394.426 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() #3: Protein | Mass: 14083.398 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() #4: Protein | Mass: 13629.911 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() #7: Protein | | Mass: 41744.570 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: USP21, USP23, PP1490 / Production host: ![]() #8: Protein | | Mass: 9036.393 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: UBB / Production host: ![]() |
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-601 DNA (145- ... , 2 types, 2 molecules IJ
| #5: DNA chain | Mass: 44520.383 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) synthetic construct (others) / Production host: ![]() |
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| #6: DNA chain | Mass: 44991.660 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) synthetic construct (others) / Production host: ![]() |
-Details
| Has protein modification | N |
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: USP21 bound to H2AK119ub nucleosome / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Molecular weight | Value: 0.3 MDa / Experimental value: NO |
| Source (natural) | Organism: Homo sapiens (human) |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| Specimen | Conc.: 0.6 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid material: GOLD / Grid mesh size: 400 divisions/in. / Grid type: Quantifoil R1.2/1.3 |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K |
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Electron microscopy imaging
| Microscopy | Model: TFS TITAN THEMIS |
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| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2500 nm / Nominal defocus min: 500 nm |
| Image recording | Electron dose: 40 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 2.98 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 83810 / Symmetry type: POINT |
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About Yorodumi




Homo sapiens (human)
United States, 1items
Citation
PDBj











































FIELD EMISSION GUN