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Open data
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Basic information
| Entry | Database: PDB / ID: 5n8y | ||||||
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| Title | KaiCBA circadian clock backbone model based on a Cryo-EM density | ||||||
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Keywords | TRANSFERASE / AAA+-ATPase / Kinase / Circadian Clock Complex / Cyanobacteria / Fold-switch | ||||||
| Function / homology | Function and homology informationdetection of redox state / negative regulation of phosphorylation / regulation of phosphorelay signal transduction system / negative regulation of circadian rhythm / entrainment of circadian clock / positive regulation of circadian rhythm / protein serine/threonine/tyrosine kinase activity / circadian rhythm / regulation of circadian rhythm / Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement ...detection of redox state / negative regulation of phosphorylation / regulation of phosphorelay signal transduction system / negative regulation of circadian rhythm / entrainment of circadian clock / positive regulation of circadian rhythm / protein serine/threonine/tyrosine kinase activity / circadian rhythm / regulation of circadian rhythm / Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement / non-specific serine/threonine protein kinase / protein serine kinase activity / protein serine/threonine kinase activity / regulation of DNA-templated transcription / magnesium ion binding / ATP hydrolysis activity / DNA binding / ATP binding / identical protein binding / plasma membrane / cytoplasm Similarity search - Function | ||||||
| Biological species | Synechococcus elongatus (bacteria) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.7 Å | ||||||
Authors | Schuller, J.M. / Snijder, J. / Loessl, P. / Heck, A.J.R. / Foerster, F. | ||||||
Citation | Journal: Science / Year: 2017Title: Structures of the cyanobacterial circadian oscillator frozen in a fully assembled state. Authors: Joost Snijder / Jan M Schuller / Anika Wiegard / Philip Lössl / Nicolas Schmelling / Ilka M Axmann / Jürgen M Plitzko / Friedrich Förster / Albert J R Heck / ![]() Abstract: Cyanobacteria have a robust circadian oscillator, known as the Kai system. Reconstituted from the purified protein components KaiC, KaiB, and KaiA, it can tick autonomously in the presence of ...Cyanobacteria have a robust circadian oscillator, known as the Kai system. Reconstituted from the purified protein components KaiC, KaiB, and KaiA, it can tick autonomously in the presence of adenosine 5'-triphosphate (ATP). The KaiC hexamers enter a natural 24-hour reaction cycle of autophosphorylation and assembly with KaiB and KaiA in numerous diverse forms. We describe the preparation of stoichiometrically well-defined assemblies of KaiCB and KaiCBA, as monitored by native mass spectrometry, allowing for a structural characterization by single-particle cryo-electron microscopy and mass spectrometry. Our data reveal details of the interactions between the Kai proteins and provide a structural basis to understand periodic assembly of the protein oscillator. | ||||||
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Structure visualization
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 5n8y.cif.gz | 648.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb5n8y.ent.gz | 427.4 KB | Display | PDB format |
| PDBx/mmJSON format | 5n8y.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 5n8y_validation.pdf.gz | 946.3 KB | Display | wwPDB validaton report |
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| Full document | 5n8y_full_validation.pdf.gz | 1002.7 KB | Display | |
| Data in XML | 5n8y_validation.xml.gz | 102.2 KB | Display | |
| Data in CIF | 5n8y_validation.cif.gz | 165.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/n8/5n8y ftp://data.pdbj.org/pub/pdb/validation_reports/n8/5n8y | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 3602MC ![]() 3603C M: map data used to model this data C: citing same article ( |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 58072.773 Da / Num. of mol.: 6 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Synechococcus elongatus (bacteria) / Gene: kaiC, Synpcc7942_1216, see0011 / Production host: ![]() References: UniProt: Q79PF4, non-specific serine/threonine protein kinase #2: Protein | Mass: 11450.387 Da / Num. of mol.: 6 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Synechococcus elongatus (bacteria) / Gene: kaiB, Synpcc7942_1217, see0010 / Production host: ![]() #3: Protein | Mass: 32666.199 Da / Num. of mol.: 12 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Synechococcus elongatus (bacteria) / Gene: kaiA, Synpcc7942_1218, see0009 / Production host: ![]() |
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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: KaiCBA circadian clock complex / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Source (natural) | Organism: Synechococcus elongatus (bacteria) |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Specimen support | Grid material: COPPER |
| Vitrification | Instrument: HOMEMADE PLUNGER / Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Alignment procedure: COMA FREE |
| Specimen holder | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Image recording | Average exposure time: 15.2 sec. / Electron dose: 45 e/Å2 / Detector mode: COUNTING / Film or detector model: GATAN K2 SUMMIT (4k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 4.7 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 32498 / Symmetry type: POINT | ||||||||||||||||||||||||||||||
| Atomic model building | Protocol: RIGID BODY FIT |
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Synechococcus elongatus (bacteria)
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