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Yorodumi- EMDB-55604: Cytoplasmic lattice filament repeat unit with the central FBXW-SK... -
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Basic information
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| Title | Cytoplasmic lattice filament repeat unit with the central FBXW-SKP1 complex | ||||||||||||
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Keywords | Ubiquitination / Complex / Filament / UNKNOWN FUNCTION | ||||||||||||
| Function / homology | Function and homology informationregulation of translation by machinery localization / cytoplasm organization / ooplasm / Signaling by BMP / Prolactin receptor signaling / embryonic process involved in female pregnancy / subcortical maternal complex / establishment of organelle localization / Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane / Cargo trafficking to the periciliary membrane ...regulation of translation by machinery localization / cytoplasm organization / ooplasm / Signaling by BMP / Prolactin receptor signaling / embryonic process involved in female pregnancy / subcortical maternal complex / establishment of organelle localization / Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane / Cargo trafficking to the periciliary membrane / Sealing of the nuclear envelope (NE) by ESCRT-III / Chromatin modifying enzymes / protein storage / structural constituent of cytoplasmic lattice / cytoplasmic lattice / cortical granule exocytosis / establishment or maintenance of apical/basal cell polarity / endoplasmic reticulum localization / Carboxyterminal post-translational modifications of tubulin / Intraflagellar transport / COPI-independent Golgi-to-ER retrograde traffic / SCF-beta-TrCP mediated degradation of Emi1 / E3 ubiquitin ligases ubiquitinate target proteins / Downregulation of SMAD2/3:SMAD4 transcriptional activity / ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA / HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand / Regulation of BACH1 activity / histone H3K18 ubiquitin ligase activity / histone H3 ubiquitin ligase activity / histone H3K14 ubiquitin ligase activity / PINK1-PRKN Mediated Mitophagy / Inactivation of CSF3 (G-CSF) signaling / histone H3K23 ubiquitin ligase activity / SCF(Skp2)-mediated degradation of p27/p21 / COPI-mediated anterograde transport / spermatogonial cell division / Regulation of TNFR1 signaling / MAP3K8 (TPL2)-dependent MAPK1/3 activation / histone H3 reader activity / Regulation of RUNX2 expression and activity / Kinesins / Degradation of GLI1 by the proteasome / IKK complex recruitment mediated by RIP1 / GSK3B-mediated proteasomal degradation of PD-L1(CD274) / Cyclin D associated events in G1 / FBXL7 down-regulates AURKA during mitotic entry and in early mitosis / cortical granule / Orc1 removal from chromatin / GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 / Dectin-1 mediated noncanonical NF-kB signaling / NIK-->noncanonical NF-kB signaling / Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha / PKR-mediated signaling / Aggrephagy / fertilization / regulation of establishment of protein localization / RHO GTPases activate IQGAPs / Mitotic Prometaphase / EML4 and NUDC in mitotic spindle formation / Degradation of beta-catenin by the destruction complex / COPI-dependent Golgi-to-ER retrograde traffic / Resolution of Sister Chromatid Cohesion / Activation of NF-kappaB in B cells / Iron uptake and transport / embryonic cleavage / The role of GTSE1 in G2/M progression after G2 checkpoint / apical cortex / positive regulation of meiotic nuclear division / chromosomal DNA methylation maintenance following DNA replication / Recycling pathway of L1 / positive regulation of embryonic development / regulation of RNA stability / intermediate filament cytoskeleton / CLEC7A (Dectin-1) signaling / FCERI mediated NF-kB activation / Interleukin-1 signaling / axonemal microtubule / F-box domain binding / Hedgehog 'off' state / RHO GTPases Activate Formins / Loss of Nlp from mitotic centrosomes / Recruitment of mitotic centrosome proteins and complexes / Loss of proteins required for interphase microtubule organization from the centrosome / Downstream TCR signaling / Separation of Sister Chromatids / Anchoring of the basal body to the plasma membrane / Recruitment of NuMA to mitotic centrosomes / AURKA Activation by TPX2 / Peroxisomal protein import / hemi-methylated DNA-binding / GLI3 is processed to GLI3R by the proteasome / embryonic pattern specification / Regulation of PLK1 Activity at G2/M Transition / regulation of epithelial cell proliferation / Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A / Neddylation / PcG protein complex / MHC class II antigen presentation / gap junction / establishment of spindle localization Similarity search - Function | ||||||||||||
| Biological species | ![]() | ||||||||||||
| Method | subtomogram averaging / cryo EM / Resolution: 7.3 Å | ||||||||||||
Authors | Singh K / Harasimov K / Carter AP | ||||||||||||
| Funding support | United Kingdom, European Union, 3 items
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Citation | Journal: EMBO J / Year: 2026Title: In-situ cryo-ET of mouse embryos reveals cytoplasmic lattices contain ubiquitin-charged E2-E3 ligase assemblies. Authors: Kashish Singh / Katarina Harasimov / Kathy K Niakan / Andrew P Carter / ![]() Abstract: Cytoplasmic lattices (CPLs) are filamentous assemblies essential for mammalian embryonic development. They are known to regulate organelle organization, spindle assembly, and protein homeostasis, but ...Cytoplasmic lattices (CPLs) are filamentous assemblies essential for mammalian embryonic development. They are known to regulate organelle organization, spindle assembly, and protein homeostasis, but their molecular functions remain unclear. Here, we develop a strategy combining cryo-focused ion beam milling and cryo-electron tomography to resolve macromolecular complexes directly in mammalian embryos. Using this approach, we determine the in situ structure of cytoplasmic lattices within 6/8-cell mouse embryos at ~4.7 Å resolution. CPL filaments are built from multiple copies of at least fourteen proteins arranged into a ~4.5 MDa repeating unit. The repeat contains a central cavity that is open at the back and lined with multiple FBXW-SKP1 complexes and three modules, each containing the E2 ubiquitin-conjugating enzyme UBE2D and the E3 ligase UHRF1. We resolve two CPL states: one is consistent with a ubiquitin-charged UBE2D, where ubiquitin is held in an open, inactive conformation by binding the scaffold protein PADI6; the second lacks discernible ubiquitin density and shows structural changes compatible with ubiquitin becoming available for transfer. Our findings support a model in which CPLs function as large ubiquitin ligase assemblies during early embryonic development. | ||||||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_55604.map.gz | 59.9 MB | EMDB map data format | |
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| Header (meta data) | emd-55604-v30.xml emd-55604.xml | 43.3 KB 43.3 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_55604_fsc.xml | 9.1 KB | Display | FSC data file |
| Images | emd_55604.png | 96.8 KB | ||
| Masks | emd_55604_msk_1.map | 64 MB | Mask map | |
| Filedesc metadata | emd-55604.cif.gz | 11.3 KB | ||
| Others | emd_55604_additional_1.map.gz emd_55604_additional_2.map.gz emd_55604_half_map_1.map.gz emd_55604_half_map_2.map.gz | 59.9 MB 59.9 MB 31.6 MB 31.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-55604 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-55604 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9t64MC ![]() 9t63C ![]() 9t65C ![]() 9t66C ![]() 9t67C ![]() 9t68C M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_55604.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 2.37 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_55604_msk_1.map | ||||||||||||
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-Additional map: Map after focussed 3D refinement of the asymmetric...
| File | emd_55604_additional_1.map | ||||||||||||
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| Annotation | Map after focussed 3D refinement of the asymmetric unit of the Cytoplasmic repeat unit of the central FBXW-SKP1 containing class | ||||||||||||
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-Additional map: Unsharpened map
| File | emd_55604_additional_2.map | ||||||||||||
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| Annotation | Unsharpened map | ||||||||||||
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-Half map: #2
| File | emd_55604_half_map_1.map | ||||||||||||
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-Half map: #1
| File | emd_55604_half_map_2.map | ||||||||||||
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Sample components
+Entire : Multi-subunit complex of the cytoplasmic lattice filament repeat unit
+Supramolecule #1: Multi-subunit complex of the cytoplasmic lattice filament repeat unit
+Macromolecule #1: KH domain-containing protein 3
+Macromolecule #2: Inactive protein-arginine deiminase type-6
+Macromolecule #3: NACHT, LRR and PYD domains-containing protein 5
+Macromolecule #4: Transducin-like enhancer protein 6
+Macromolecule #5: Oocyte-expressed protein homolog
+Macromolecule #6: Zinc finger BED domain-containing protein 3
+Macromolecule #7: NLR family, pyrin domain containing 4F
+Macromolecule #8: NACHT, LRR and PYD domains-containing protein 14
+Macromolecule #9: E3 ubiquitin-protein ligase UHRF1
+Macromolecule #10: Ubiquitin-conjugating enzyme E2 D3
+Macromolecule #11: Tubulin alpha-1C chain
+Macromolecule #12: Tubulin beta-4B chain
+Macromolecule #13: F-box/WD repeat-containing protein
+Macromolecule #14: S-phase kinase-associated protein 1
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | subtomogram averaging |
| Aggregation state | filament |
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Sample preparation
| Buffer | pH: 7.5 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 3.5 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 4.0 µm / Nominal defocus min: 1.0 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Authors
United Kingdom, European Union, 3 items
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Processing
FIELD EMISSION GUN

