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Yorodumi- PDB-9e14: Full-length human dynein-1 in phi-like comformation bound to a Li... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9.0E+14 | ||||||
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| Title | Full-length human dynein-1 in phi-like comformation bound to a Lis1 dimer under Nde1-Lis1 condition | ||||||
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Keywords | MOTOR PROTEIN / dynein-1 / phi-like conformation / Lis1 | ||||||
| Function / homology | Function and homology informationintracellular transport of viral protein in host cell / corpus callosum morphogenesis / nitric-oxide synthase inhibitor activity / microtubule cytoskeleton organization involved in establishment of planar polarity / ameboidal-type cell migration / establishment of planar polarity of embryonic epithelium / secretory vesicle / 1-alkyl-2-acetylglycerophosphocholine esterase complex / deoxyribonuclease inhibitor activity / negative regulation of DNA strand resection involved in replication fork processing ...intracellular transport of viral protein in host cell / corpus callosum morphogenesis / nitric-oxide synthase inhibitor activity / microtubule cytoskeleton organization involved in establishment of planar polarity / ameboidal-type cell migration / establishment of planar polarity of embryonic epithelium / secretory vesicle / 1-alkyl-2-acetylglycerophosphocholine esterase complex / deoxyribonuclease inhibitor activity / negative regulation of DNA strand resection involved in replication fork processing / maintenance of centrosome location / negative regulation of phosphorylation / platelet activating factor metabolic process / transport along microtubule / intraciliary retrograde transport / visual behavior / radial glia-guided pyramidal neuron migration / acrosome assembly / central region of growth cone / cerebral cortex neuron differentiation / dynein light chain binding / establishment of centrosome localization / microtubule sliding / dynein heavy chain binding / positive regulation of cytokine-mediated signaling pathway / Activation of BIM and translocation to mitochondria / motile cilium assembly / positive regulation of embryonic development / microtubule organizing center organization / interneuron migration / layer formation in cerebral cortex / ciliary tip / astral microtubule / auditory receptor cell development / nuclear membrane disassembly / Intraflagellar transport / positive regulation of intracellular transport / cortical microtubule organization / negative regulation of nitric oxide biosynthetic process / positive regulation of dendritic spine morphogenesis / reelin-mediated signaling pathway / myeloid leukocyte migration / regulation of metaphase plate congression / positive regulation of spindle assembly / establishment of spindle localization / regulation of G protein-coupled receptor signaling pathway / stereocilium / osteoclast development / microtubule plus-end binding / microtubule-dependent intracellular transport of viral material towards nucleus / brain morphogenesis / vesicle transport along microtubule / dynein complex / COPI-independent Golgi-to-ER retrograde traffic / retrograde axonal transport / kinesin complex / P-body assembly / microtubule motor activity / negative regulation of JNK cascade / minus-end-directed microtubule motor activity / microtubule associated complex / cytoplasmic dynein complex / dynein light intermediate chain binding / centrosome localization / motile cilium / stem cell division / neuromuscular process controlling balance / microtubule-based movement / nuclear migration / Macroautophagy / cell leading edge / dynein intermediate chain binding / dynein complex binding / germ cell development / transmission of nerve impulse / establishment of mitotic spindle orientation / dynactin binding / tertiary granule membrane / protein secretion / cochlea development / ficolin-1-rich granule membrane / spermatid development / neuroblast proliferation / enzyme inhibitor activity / positive regulation of insulin secretion involved in cellular response to glucose stimulus / positive regulation of axon extension / microtubule-based process / lipid catabolic process / phospholipase binding / COPI-mediated anterograde transport / cytoplasmic microtubule / JNK cascade / Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal / cytoplasmic microtubule organization / axon cytoplasm / Mitotic Prometaphase / EML4 and NUDC in mitotic spindle formation / Loss of Nlp from mitotic centrosomes / Loss of proteins required for interphase microtubule organization from the centrosome / stress granule assembly Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 5 Å | ||||||
Authors | Yang, J. / Zhang, K. | ||||||
| Funding support | United States, 1items
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Citation | Journal: Nat Chem Biol / Year: 2025Title: Nde1 promotes Lis1 binding to full-length autoinhibited human dynein 1. Authors: Jun Yang / Yuanchang Zhao / Pengxin Chai / Ahmet Yildiz / Kai Zhang / ![]() Abstract: Cytoplasmic dynein 1 (dynein) is the primary motor responsible for the retrograde transport of intracellular cargoes along microtubules. Activation of dynein requires the opening its autoinhibited ...Cytoplasmic dynein 1 (dynein) is the primary motor responsible for the retrograde transport of intracellular cargoes along microtubules. Activation of dynein requires the opening its autoinhibited Phi conformation, a process driven by Lis1 and Nde1/Ndel1. Using biochemical reconstitution and cryo-electron microscopy, we demonstrate that Nde1 enhances Lis1 binding to autoinhibited dynein and facilitates Phi opening. We identify a key intermediate in this activation pathway where a single Lis1 dimer binds between Phi-like (Phi) motor rings. In this 'Phi-Lis1' complex, Lis1 interacts with one motor domain through canonical sites at the AAA+ (adenosine triphosphatases associated with diverse cellular activities) ring and stalk, and with AAA5, AAA6 and linker regions of the other motor domain. Mutagenesis and motility assays confirm the critical role of the Phi-Lis1 interface in dynein activation. This intermediate forms rapidly in the presence of Nde1, although Nde1 is not part of Phi-Lis1. These findings provide key insights into how Nde1 promotes Lis1-mediated Phi opening. | ||||||
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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 | 9e14.cif.gz | 2 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb9e14.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 9e14.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9e14_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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| Full document | 9e14_full_validation.pdf.gz | 1.4 MB | Display | |
| Data in XML | 9e14_validation.xml.gz | 272.7 KB | Display | |
| Data in CIF | 9e14_validation.cif.gz | 429.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/e1/9e14 ftp://data.pdbj.org/pub/pdb/validation_reports/e1/9e14 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 47383MC ![]() 9e0zC ![]() 9e10C ![]() 9e11C ![]() 9e12C ![]() 9e13C 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
-Cytoplasmic dynein 1 ... , 3 types, 6 molecules ABCDEF
| #1: Protein | Mass: 533083.250 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: DYNC1H1, DHC1, DNCH1, DNCL, DNECL, DYHC, KIAA0325 / Production host: ![]() #2: Protein | Mass: 71546.445 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: DYNC1I2, DNCI2, DNCIC2 / Production host: ![]() #3: Protein | Mass: 54173.156 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: DYNC1LI2, DNCLI2, LIC2 / Production host: ![]() |
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-Dynein light chain ... , 3 types, 6 molecules GHIJKL
| #4: Protein | Mass: 10934.576 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: DYNLRB1, BITH, DNCL2A, DNLC2A, ROBLD1, HSPC162 / Production host: ![]() #5: Protein | Mass: 10381.899 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: DYNLL1, DLC1, DNCL1, DNCLC1, HDLC1 / Production host: ![]() #6: Protein | Mass: 12461.996 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: DYNLT1, TCTEL1, TCTEX-1, TCTEX1 / Production host: ![]() |
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-Protein , 1 types, 2 molecules OP
| #7: Protein | Mass: 46709.984 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: PAFAH1B1, LIS1, MDCR, MDS, PAFAHA / Production host: ![]() |
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-Non-polymers , 3 types, 12 molecules 




| #8: Chemical | ChemComp-ADP / #9: Chemical | #10: Chemical | ChemComp-MG / |
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-Details
| Has ligand of interest | Y |
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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: Full-length human dynein-1 in phi-like comformation bound to a Lis1 dimer under Nde1-Lis1 condition Type: COMPLEX / Entity ID: #1-#7 / Source: RECOMBINANT |
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| Molecular weight | Value: 1.5 MDa / Experimental value: YES |
| Source (natural) | Organism: Homo sapiens (human) |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.2 Details: 25 mM HEPES pH 7.2, 150 mM KCl, 1 mM MgCl2, 5 mM DTT, 3 mM ATP |
| Specimen | Conc.: 2 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 278 K |
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Electron microscopy imaging
| Microscopy | Model: TFS GLACIOS |
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| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 45000 X / Calibrated magnification: 45000 X / Nominal defocus max: 2600 nm / Nominal defocus min: 1200 nm / Calibrated defocus min: 1200 nm / Calibrated defocus max: 2600 nm / Cs: 2.7 mm / C2 aperture diameter: 30 µm |
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Image recording | Electron dose: 40 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||
| 3D reconstruction | Resolution: 5 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 61684 / Symmetry type: POINT |
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About Yorodumi



Homo sapiens (human)
United States, 1items
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FIELD EMISSION GUN