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Yorodumi- EMDB-1940: Negative stain EM density of green-type rubisco activase (R294V) ... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-1940 | |||||||||
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Title | Negative stain EM density of green-type rubisco activase (R294V) from tobacco | |||||||||
Map data | Negative stain EM density of green-type rubisco activase from tobacco. Hexameric model based on p97 D2 ring is fitted into the structure. | |||||||||
Sample |
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Keywords | green type rubisco activase / AAA+ protein / ATPase / negative stain EM | |||||||||
Function / homology | Function and homology information ribulose-1,5-bisphosphate carboxylase/oxygenase activator activity / chloroplast stroma / ATP hydrolysis activity / ATP binding / identical protein binding Similarity search - Function | |||||||||
Biological species | Nicotiana tabacum (common tobacco) | |||||||||
Method | single particle reconstruction / negative staining / Resolution: 20.0 Å | |||||||||
Authors | Stotz M / Mueller-Cajar O / Ciniawsky S / Wendler P / Hartl FU / Bracher A / Hayer-Hartl M | |||||||||
Citation | Journal: Nat Struct Mol Biol / Year: 2011 Title: Structure of green-type Rubisco activase from tobacco. Authors: Mathias Stotz / Oliver Mueller-Cajar / Susanne Ciniawsky / Petra Wendler / F Ulrich Hartl / Andreas Bracher / Manajit Hayer-Hartl / Abstract: Rubisco, the enzyme that catalyzes the fixation of atmospheric CO(2) in photosynthesis, is subject to inactivation by inhibitory sugar phosphates. Here we report the 2.95-Å crystal structure of ...Rubisco, the enzyme that catalyzes the fixation of atmospheric CO(2) in photosynthesis, is subject to inactivation by inhibitory sugar phosphates. Here we report the 2.95-Å crystal structure of Nicotiana tabacum Rubisco activase (Rca), the enzyme that facilitates the removal of these inhibitors. Rca from tobacco has a classical AAA(+)-protein domain architecture. Although Rca populates a range of oligomeric states when in solution, it forms a helical arrangement with six subunits per turn when in the crystal. However, negative-stain electron microscopy of the active mutant R294V suggests that Rca functions as a hexamer. The residues determining species specificity for Rubisco are located in a helical insertion of the C-terminal domain and probably function in conjunction with the N-domain in Rubisco recognition. Loop segments exposed toward the central pore of the hexamer are required for the ATP-dependent remodeling of Rubisco, resulting in the release of inhibitory sugar. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_1940.map.gz | 147.1 KB | EMDB map data format | |
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Header (meta data) | emd-1940-v30.xml emd-1940.xml | 10.2 KB 10.2 KB | Display Display | EMDB header |
Images | emd-1940.png | 122 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-1940 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1940 | HTTPS FTP |
-Validation report
Summary document | emd_1940_validation.pdf.gz | 186.7 KB | Display | EMDB validaton report |
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Full document | emd_1940_full_validation.pdf.gz | 185.9 KB | Display | |
Data in XML | emd_1940_validation.xml.gz | 5.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1940 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1940 | HTTPS FTP |
-Related structure data
Related structure data | 3zw6MC 3t15C M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_1940.map.gz / Format: CCP4 / Size: 7.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Negative stain EM density of green-type rubisco activase from tobacco. Hexameric model based on p97 D2 ring is fitted into the structure. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 3.308 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : Nicotiana tabacum Rubisco Activase (R294V)
Entire | Name: Nicotiana tabacum Rubisco Activase (R294V) |
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Components |
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-Supramolecule #1000: Nicotiana tabacum Rubisco Activase (R294V)
Supramolecule | Name: Nicotiana tabacum Rubisco Activase (R294V) / type: sample / ID: 1000 / Oligomeric state: Hexamer / Number unique components: 1 |
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Molecular weight | Experimental: 300 KDa / Theoretical: 300 KDa / Method: DSS cross linking, gel filtration |
-Macromolecule #1: Ribulose bisphosphate carboxylase activase 1, chloroplastic
Macromolecule | Name: Ribulose bisphosphate carboxylase activase 1, chloroplastic type: protein_or_peptide / ID: 1 / Name.synonym: Rubisco Activase (Rca) Details: Hexamer assembles upon addition of 1 mM ATPgammaS at 25 deg C Number of copies: 6 / Oligomeric state: Hexamer / Recombinant expression: Yes |
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Source (natural) | Organism: Nicotiana tabacum (common tobacco) / synonym: Common tobacco / Organelle: Chloroplast |
Molecular weight | Experimental: 300 KDa / Theoretical: 300 KDa |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) / Recombinant plasmid: pHUENtRca |
Sequence | InterPro: ATPase, AAA-type, core |
-Experimental details
-Structure determination
Method | negative staining |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.044 mg/mL |
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Buffer | pH: 8 / Details: 20mM Tris-HCl, 50mM NaCl, 2mM MgCl2,1mM ATPgammaS |
Staining | Type: NEGATIVE Details: Grids were stained twice with 2% w/v uranyl acetate |
Grid | Details: Plain carbon |
Vitrification | Cryogen name: NONE / Instrument: OTHER |
-Electron microscopy
Microscope | FEI TECNAI 12 |
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Alignment procedure | Legacy - Astigmatism: Objective lens astigmatism was corrected for at 110k magnification |
Date | Jun 22, 2011 |
Image recording | Category: CCD / Film or detector model: FEI EAGLE (2k x 2k) / Average electron dose: 20 e/Å2 |
Electron beam | Acceleration voltage: 120 kV / Electron source: LAB6 |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.0 mm / Nominal defocus max: 0.95 µm / Nominal defocus min: 0.47 µm |
Sample stage | Specimen holder: Single tilt / Specimen holder model: SIDE ENTRY, EUCENTRIC |
-Image processing
CTF correction | Details: Phase flipping, each particle |
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Final reconstruction | Applied symmetry - Point group: C6 (6 fold cyclic) / Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 20.0 Å / Resolution method: FSC 0.5 CUT-OFF / Software - Name: MRC, IMAGIC, SPIDER / Number images used: 599 |
-Atomic model buiding 1
Initial model | PDB ID: |
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Software | Name: Chimera |
Details | Protocol: Rigid body. A module of alpha helical domain and alpha-beta domain of neighbouring subunit was overlaid with p97 D2 (3CF3) structure and the hexamer was fitted into the EM map |
Refinement | Space: REAL / Protocol: RIGID BODY FIT / Target criteria: Local minimisation, fit in map |
Output model | PDB-3zw6: |