[English] 日本語
Yorodumi- PDB-9e14: Full-length human dynein-1 in phi-like comformation bound to a Li... -
+
Open data
-
Basic information
| Entry | Database: PDB / ID: 9.0E+14 | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Title | Full-length human dynein-1 in phi-like comformation bound to a Lis1 dimer under Nde1-Lis1 condition | |||||||||||||||||||||
Components |
| |||||||||||||||||||||
Keywords | MOTOR PROTEIN / dynein-1 / phi-like conformation / Lis1 | |||||||||||||||||||||
| Function / homology | Function and homology informationintracellular transport of viral protein in host cell / nitric-oxide synthase inhibitor activity / microtubule cytoskeleton organization involved in establishment of planar polarity / establishment of planar polarity of embryonic epithelium / 1-alkyl-2-acetylglycerophosphocholine esterase complex / negative regulation of DNA strand resection involved in replication fork processing / secretory vesicle / corpus callosum morphogenesis / negative regulation of phosphorylation / maintenance of centrosome location ...intracellular transport of viral protein in host cell / nitric-oxide synthase inhibitor activity / microtubule cytoskeleton organization involved in establishment of planar polarity / establishment of planar polarity of embryonic epithelium / 1-alkyl-2-acetylglycerophosphocholine esterase complex / negative regulation of DNA strand resection involved in replication fork processing / secretory vesicle / corpus callosum morphogenesis / negative regulation of phosphorylation / maintenance of centrosome location / ameboidal-type cell migration / intraciliary retrograde transport / platelet activating factor metabolic process / visual behavior / radial glia-guided pyramidal neuron migration / establishment of centrosome localization / central region of growth cone / cerebral cortex neuron differentiation / acrosome assembly / nuclear membrane disassembly / microtubule sliding / dynein light chain binding / transport along microtubule / dynein heavy chain binding / Activation of BIM and translocation to mitochondria / positive regulation of cytokine-mediated signaling pathway / motile cilium assembly / positive regulation of embryonic development / microtubule organizing center organization / interneuron migration / layer formation in cerebral cortex / astral microtubule / auditory receptor cell development / cortical microtubule organization / Intraflagellar transport / myeloid leukocyte migration / reelin-mediated signaling pathway / positive regulation of intracellular transport / regulation of metaphase plate congression / positive regulation of spindle assembly / positive regulation of dendritic spine morphogenesis / negative regulation of nitric oxide biosynthetic process / establishment of spindle localization / osteoclast development / regulation of G protein-coupled receptor signaling pathway / stereocilium / microtubule plus-end binding / microtubule-dependent intracellular transport of viral material towards nucleus / brain morphogenesis / motile cilium / vesicle transport along microtubule / retrograde axonal transport / COPI-independent Golgi-to-ER retrograde traffic / P-body assembly / minus-end-directed microtubule motor activity / microtubule associated complex / negative regulation of JNK cascade / centrosome localization / dynein light intermediate chain binding / cytoplasmic dynein complex / microtubule motor activity / kinesin complex / neuromuscular process controlling balance / stem cell division / microtubule-based movement / nuclear migration / Macroautophagy / establishment of mitotic spindle orientation / dynein intermediate chain binding / germ cell development / cell leading edge / transmission of nerve impulse / dynein complex binding / tertiary granule membrane / neuroblast proliferation / dynactin binding / cochlea development / ficolin-1-rich granule membrane / protein secretion / spermatid development / positive regulation of axon extension / microtubule-based process / lipid catabolic process / COPI-mediated anterograde transport / phospholipase binding / cytoplasmic microtubule / JNK cascade / cytoplasmic microtubule organization / Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal / axon cytoplasm / Loss of Nlp from mitotic centrosomes / Loss of proteins required for interphase microtubule organization from the centrosome / Recruitment of mitotic centrosome proteins and complexes / MHC class II antigen presentation / positive regulation of mitotic cell cycle / Recruitment of NuMA to mitotic centrosomes / Anchoring of the basal body to the plasma membrane / substantia nigra development / Mitotic Prometaphase / EML4 and NUDC in mitotic spindle formation 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
| |||||||||||||||||||||
Citation | Journal: Nat Chem Biol / Year: 2026Title: 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. | |||||||||||||||||||||
| History |
|
-
Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
|---|
-
Downloads & links
-
Download
| PDBx/mmCIF format | 9e14.cif.gz | 2 MB | Display | PDBx/mmCIF format |
|---|---|---|---|---|
| PDB format | pdb9e14.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 9e14.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| 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 |
|---|---|
| Similar structure data | Similarity search - Function & homology F&H Search |
-
Links
-
Assembly
| Deposited unit | ![]()
|
|---|---|
| 1 |
|
-
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: ![]() |
|---|
-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: ![]() |
|---|
-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: ![]() |
|---|
-Non-polymers , 3 types, 12 molecules 




| #8: Chemical | ChemComp-ADP / #9: Chemical | #10: Chemical | ChemComp-MG / |
|---|
-Details
| Has ligand of interest | Y |
|---|---|
| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
|---|---|
| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-
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 |
|---|---|
| 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 |
-
Electron microscopy imaging
| Microscopy | Model: TFS GLACIOS |
|---|---|
| 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) |
-
Processing
| EM software |
| ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
Movie
Controller
About Yorodumi



Homo sapiens (human)
United States, 1items
Citation
















PDBj




















FIELD EMISSION GUN