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Open data
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Basic information
| Entry | Database: PDB / ID: 9rwz | |||||||||||||||
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| Title | ZSWIM8-CUL3 complex bound to AGO2-miR-7-CYRANO | |||||||||||||||
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Keywords | LIGASE / miRNA / E3 Ligase | |||||||||||||||
| Function / homology | Function and homology informationpositive regulation of miRNA catabolic process / positive regulation of mitotic cell cycle phase transition / POZ domain binding / : / endoribonuclease activity, cleaving miRNA-paired mRNA / endoribonuclease activity, cleaving siRNA-paired mRNA / siRNA-mediated gene silencing by mRNA destabilization / Post-transcriptional silencing by small RNAs / Competing endogenous RNAs (ceRNAs) regulate PTEN translation / Regulation of CDH11 mRNA translation by microRNAs ...positive regulation of miRNA catabolic process / positive regulation of mitotic cell cycle phase transition / POZ domain binding / : / endoribonuclease activity, cleaving miRNA-paired mRNA / endoribonuclease activity, cleaving siRNA-paired mRNA / siRNA-mediated gene silencing by mRNA destabilization / Post-transcriptional silencing by small RNAs / Competing endogenous RNAs (ceRNAs) regulate PTEN translation / Regulation of CDH11 mRNA translation by microRNAs / Regulation of NPAS4 mRNA translation / Regulation of PTEN mRNA translation / miRNA-mediated gene silencing by mRNA destabilization / negative regulation of amyloid precursor protein biosynthetic process / negative regulation of Rho protein signal transduction / embryonic cleavage / polar microtubule / Small interfering RNA (siRNA) biogenesis / anaphase-promoting complex-dependent catabolic process / Regulation of CDH1 mRNA translation by microRNAs / nuclear protein quality control by the ubiquitin-proteasome system / positive regulation of trophoblast cell migration / regulation protein catabolic process at postsynapse / COPII vesicle coat assembly / Transcriptional Regulation by MECP2 / Regulation of PD-L1(CD274) translation / RISC-loading complex / cell projection organization / RHOBTB3 ATPase cycle / mRNA cap binding / miRNA processing / RISC complex assembly / regulatory ncRNA-mediated post-transcriptional gene silencing / miRNA-mediated gene silencing by inhibition of translation / stem cell division / pre-miRNA processing / RNA 7-methylguanosine cap binding / regulation of synapse maturation / siRNA binding / mRNA 3'-UTR AU-rich region binding / target-directed miRNA degradation / M-decay: degradation of maternal mRNAs by maternally stored factors / positive regulation of mitotic metaphase/anaphase transition / Regulation of MITF-M-dependent genes involved in apoptosis / elongin complex / RISC complex / TGFBR3 expression / regulatory ncRNA-mediated gene silencing / Notch binding / Regulation of RUNX1 Expression and Activity / stress fiber assembly / P-body assembly / miRNA binding / RHOBTB1 GTPase cycle / VCB complex / MicroRNA (miRNA) biogenesis / positive regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay / Cul5-RING ubiquitin ligase complex / ubiquitin-dependent protein catabolic process via the C-end degron rule pathway / Cul2-RING ubiquitin ligase complex / negative regulation of DNA-templated DNA replication / Cul3-RING ubiquitin ligase complex / negative regulation of type I interferon production / positive regulation of cytokinesis / positive regulation of nuclear-transcribed mRNA poly(A) tail shortening / RNA polymerase II complex binding / ubiquitin ligase complex scaffold activity / protein quality control for misfolded or incompletely synthesized proteins / Pausing and recovery of Tat-mediated HIV elongation / Tat-mediated HIV elongation arrest and recovery / HIV elongation arrest and recovery / Pausing and recovery of HIV elongation / Regulation of MECP2 expression and activity / protein monoubiquitination / endoplasmic reticulum to Golgi vesicle-mediated transport / mitotic metaphase chromosome alignment / Tat-mediated elongation of the HIV-1 transcript / Formation of HIV-1 elongation complex containing HIV-1 Tat / RHOBTB2 GTPase cycle / core promoter sequence-specific DNA binding / sperm flagellum / Formation of HIV elongation complex in the absence of HIV Tat / NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux / protein autoubiquitination / ubiquitin-like ligase-substrate adaptor activity / RNA Polymerase II Transcription Elongation / Formation of RNA Pol II elongation complex / kidney development / intrinsic apoptotic signaling pathway / ribosome-associated ubiquitin-dependent protein catabolic process / Nuclear events stimulated by ALK signaling in cancer / RNA endonuclease activity / RNA Polymerase II Pre-transcription Events / protein K48-linked ubiquitination / regulation of cellular response to insulin stimulus / positive regulation of TORC1 signaling / translation initiation factor activity / gene expression / negative regulation of translational initiation / integrin-mediated signaling pathway Similarity search - Function | |||||||||||||||
| Biological species | Homo sapiens (human) | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.1 Å | |||||||||||||||
Authors | Farnung, J. / Slobodyanyuk, E. / Bartel, D.P. / Schulman, B.A. | |||||||||||||||
| Funding support | European Union, Germany, 2items
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Citation | Journal: Nature / Year: 2026Title: The E3 ubiquitin ligase mechanism specifying targeted microRNA degradation. Authors: Jakob Farnung / Elena Slobodyanyuk / Peter Y Wang / Lianne W Blodgett / Daniel H Lin / Susanne von Gronau / Brenda A Schulman / David P Bartel / ![]() Abstract: MicroRNAs (miRNAs) associate with Argonaute (AGO) proteins to form complexes that down-regulate target RNAs, including messenger RNAs from most human genes. Within each complex, the miRNA pairs to ...MicroRNAs (miRNAs) associate with Argonaute (AGO) proteins to form complexes that down-regulate target RNAs, including messenger RNAs from most human genes. Within each complex, the miRNA pairs to target RNAs, and AGO provides effector function while also protecting the miRNA from cellular nucleases. Although much is known about miRNA-directed gene regulation, less is known about how miRNAs themselves are regulated. One pathway that regulates miRNAs involves unusual targets called 'trigger' RNAs, which reverse the canonical regulatory logic and instead down-regulate miRNAs. This target-directed miRNA degradation (TDMD) is thought to require a cullin-RING E3 ligase because it depends on the cullin protein CUL3 and other ubiquitylation components, including the BC-box protein ZSWIM8 (refs. ). ZSWIM8 is required for murine perinatal viability and for destabilization of most short-lived miRNAs, which suggests biological importance of TDMD. Here, biochemical and cellular assays establish AGO binding and polyubiquitylation by the ZSWIM8-CUL3 E3 ligase as the key regulatory steps of TDMD, and thereby define a unique cullin-RING E3 ligase class. Cryogenic electron microscopy analyses show ZSWIM8 recognizing distinct AGO and RNA conformations shaped by pairing of the miRNA to the trigger. Specificity of AGO ubiquitylation is established through generalizable RNA-RNA, RNA-protein and protein-protein interactions. The substrate features recognized by the E3 ligase do not conform to a conventional degron but instead establish a two-RNA-factor authentication mechanism for specifying a protein ubiquitylation substrate. | |||||||||||||||
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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 | 9rwz.cif.gz | 767.9 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9rwz.ent.gz | 585.4 KB | Display | PDB format |
| PDBx/mmJSON format | 9rwz.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/rw/9rwz ftp://data.pdbj.org/pub/pdb/validation_reports/rw/9rwz | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 54352MC C: citing same article ( M: map data used to model this data |
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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 , 5 types, 9 molecules ABCDEHINM
| #1: Protein | Mass: 98554.383 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: N-terminal hexahistidine purification tag was not removed. Source: (gene. exp.) Homo sapiens (human) / Gene: AGO2, EIF2C2Production host: Spodoptera aff. frugiperda 1 BOLD-2017 (butterflies/moths)References: UniProt: Q9UKV8, Hydrolases; Acting on ester bonds; Endoribonucleases producing 5'-phosphomonoesters | ||||||
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| #2: Protein | Mass: 13147.781 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: ELOB, TCEB2Production host: Spodoptera aff. frugiperda 1 BOLD-2017 (butterflies/moths)References: UniProt: Q15370 #3: Protein | Mass: 12485.135 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: ELOC, TCEB1Production host: Spodoptera aff. frugiperda 1 BOLD-2017 (butterflies/moths)References: UniProt: Q15369 #5: Protein | Mass: 46410.113 Da / Num. of mol.: 2 / Mutation: I342R, L346D Source method: isolated from a genetically manipulated source Details: CUL3 NTD containing solubilizing mutations I342R, L346D, and remnant of C-terminal TEV protease cleavage site. Source: (gene. exp.) Homo sapiens (human) / Gene: CUL3, KIAA0617 / Production host: ![]() #7: Protein | Mass: 200458.016 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Details: C-terminal twin-strep purification tag was not removed. Source: (gene. exp.) Homo sapiens (human) / Gene: ZSWIM8, KIAA0913 / Production host: Spodoptera (butterflies/moths) / References: UniProt: A7E2V4 |
-RNA chain , 2 types, 2 molecules GT
| #4: RNA chain | Mass: 7690.520 Da / Num. of mol.: 1 / Source method: obtained synthetically / Details: 5' terminus is phosphorylated / Source: (synth.) Homo sapiens (human) |
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| #6: RNA chain | Mass: 38577.793 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human) / References: GenBank: 2994212338 |
-Non-polymers , 1 types, 2 molecules 
| #8: Chemical |
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-Details
| Has ligand of interest | N |
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| Has protein modification | N |
-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: CYRANO-AGO2-miR-7 in complex with ZSWIM8-ELONGIN B/C, CUL3 Type: COMPLEX Details: Complex formed of CYRANO-AGO2-miR-7 in complex with ZSWIM8-ELONGIN B/C, CUL3 Entity ID: #1-#7 / Source: RECOMBINANT |
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| Molecular weight | Experimental value: NO |
| Source (natural) | Organism: Homo sapiens (human) |
| Source (recombinant) | Organism: Spodoptera aff. frugiperda 1 BOLD-2017 (butterflies/moths) |
| Buffer solution | pH: 7.8 / Details: 25 mM HEPES, 50 mM NaCl, 1 mM TCEP, pH 7.8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE-PROPANE / Humidity: 95 % / Chamber temperature: 277 K |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: TFS KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 105000 X / Nominal defocus max: 2000 nm / Nominal defocus min: 500 nm |
| Image recording | Electron dose: 58 e/Å2 / Film or detector model: GATAN K3 BIOCONTINUUM (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||
| 3D reconstruction | Resolution: 3.1 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 230859 / Symmetry type: POINT |
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About Yorodumi




Homo sapiens (human)
Germany, 2items
Citation





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Spodoptera aff. frugiperda 1 BOLD-2017 (butterflies/moths)

FIELD EMISSION GUN