Pyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate
by single particle reconstruction, at 13.2 A resolution

#1: Surface view with section colored by density value, Surface level: 2.65, Made by UCSF CHIMERA
#2: Surface view colored by cylindrical radius, Surface level: 2.65, Made by UCSF CHIMERA
Entry | |
| Summary | |
| Database / ID | EM DATA BANK (EMDB) / 1737 |
|---|---|
| Title | Pyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate |
| Map | Pyruvate carboxylase from S.aureus after addition of acetyl-CoA, AMP-PNP and pyruvate |
| Sample | Pyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate |
| Keywords | Pyruvate carboxylase, biotin-dependent carobxylase, acetyl-CoA, multifunctional, pyruvate, oxaloacetate, EC 6.4.1.1, Ligase |
| Authors | Lasso G, Yu LPC, Gil D, Xiang S, Tong L, Valle M |
| Date | Deposition: 2010-06-01, Header release: 2010-06-11, Map release: 2011-05-19, Last update: 2011-05-19 |
| EMDB Sites | EMDB @PDBe (EU), EMDB @RCSB (USA) |
| Structure Visualization | |
| Movies | Movie Page#1: Surface view with section colored by density value, Surface level: 2.65, Made by UCSF CHIMERA #2: Surface view colored by cylindrical radius, Surface level: 2.65, Made by UCSF CHIMERA |
| Supplemental images | |
| Structure viewers | Yorodumi, Launch PeppeR (About PeppeR), Volume viewer (RCSB, PDBe) |
| Related Structure Data | |
| Related Entries |
Cite: data citing same article |
| Similar strucutres (beta) |
List of similar structure data about Omokage system |
Article | |
| Citation - Primary | |
| Article | Structure, Vol. 18, Issue 10, Page 1300-10, Year 2010 |
|---|---|
| Title | Cryo-EM analysis reveals new insights into the mechanism of action of pyruvate carboxylase. |
| Authors | Gorka Lasso, Linda P C Yu, David Gil, Song Xiang, Liang Tong, Mikel Valle Structural Biology Unit, Center for Cooperative Research in Biosciences bioGUNE, 48160 Derio, Spain. |
| Keywords | Bacterial Proteins (chemistry), Binding Sites, Carbon-Nitrogen Ligases (chemistry, 6.3.-), Carboxyl and Carbamoyl Transferases (chemistry, 2.1.3.-), Catalytic Domain, Cryoelectron Microscopy, Crystallography, X-Ray, Models, Molecular, Protein Binding, Protein Folding, Protein Multimerization, Protein Structure, Tertiary, Pyruvate Carboxylase (chemistry, 6.4.1.1), Recombinant Proteins (chemistry), Staphylococcus aureus (enzymology), Substrate Specificity, biotin carboxylase ( 6.3.4.14) |
| Links | PII: S0969-2126(10)00297-2, DOI: 10.1016/j.str.2010.07.008, PubMed: 20947019, PMC: PMC2956116 |
Map | |||||||||||||||||||||||||
| File | EMD-1737.map ( map file in CCP4 format, 6574 KB ) | ||||||||||||||||||||||||
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| Projections & Slices | Size of images:
Images are generated by Spider package. | ||||||||||||||||||||||||
| Density |
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| Data Type | Image stored as Reals | ||||||||||||||||||||||||
| Space Group Number | 1 | ||||||||||||||||||||||||
| Map Geometry |
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| Unit Cell | A= B= C: 332.76 A Alpha=beta=gamma: 90 degrees | ||||||||||||||||||||||||
| Pixel Spacing | X= Y= Z: 2.82 A | ||||||||||||||||||||||||
| CCP4 map header info | |||||||||||||||||||||||||
| Annotation Details | Pyruvate carboxylase from S.aureus after addition of acetyl-CoA, AMP-PNP and pyruvate | ||||||||||||||||||||||||
Supplement | |
| Images | |
| Images | |
|---|---|
Sample | |
| Name | Pyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate |
|---|---|
| Number of Components | 1 |
| Oligomeric State | Homotetramer |
| Theoretical Mass | 0.52MDa |
| Component #1: protein - PC | |
| Scientific name | Pyruvate carboxylase |
| Common Name | PC |
| Theoretical Mass | 0.52 MDa |
| Oligomeric Details | Homotetramer |
| Scientific Name of Species | Staphylococcus aureus |
| NCBI taxonomy | 1280 |
| Recombinant expression | Yes |
| Engineered Source | Vector: pET28a Expression system: Escherichia coli BL21 Star |
Experiment | |
| Sample Preparation | |
| Specimen Conc | 0.1 mg/ml |
|---|---|
| Specimen Support Details | Quantifoil R2/2, 100 holey carbon films, cu 200 mesh |
| Specimen State | particle |
| Buffer | Details: 20 mM Tris-HCl, 2mM NaCl, 2mM DTT, 2mM acetyl-CoA, 2mM AMP-PNP, 50 Mm KHCO3, 1m mM pyruvate pH: 7.5 |
| Vitrification | |
| Method | Blot for 1.5 seconds |
| Cryogen Name | ETHANE |
| Time Resolved State | 45 sec |
| Details | Vitrification instrument: Vitrobot (FEI) |
| Humidity | 100 |
| Instrument | FEI VITROBOT |
| Temperature | 277 Kelvin |
| Imaging | |
| Microscope | JEOL 2200FS |
| Electron Gun | |
| Electron Source | FIELD EMISSION GUN |
| Accelerating Voltage | 200 kV |
| Electron Dose | 11 e/A**2 |
| Illumination Mode | FLOOD BEAM |
| Lens | |
| Magnification | Nominal: 50000 |
| Nominal Cs | 2 mm |
| Imaging Mode | BRIGHT FIELD |
| Defocus | 899 nm - 5544 nm |
| Energy Filter | Energy Filter: Omega |
| Specimen Holder | |
| Holder | single tilt cryoholder |
| Model | GATAN LIQUID NITROGEN |
| Temperature | 99 K |
| Camera | |
| Detector | Kodak film SO-163 |
| Image Acquisition | |
| Scanner | ZEISS SCAI |
| Number of Digital Images | 32 |
| Sampling Size | 2.82 |
Processing | |
| Method | single particle reconstruction |
|---|---|
| 3D reconstruction | |
| Algorithm | Single particle |
| Euler Angles Details | Spider |
| Software | Spider |
| CTF Correction | By defocus groups (Wiener filter) |
| Resolution By Author | 13.2 A |
| Resolution Method | FSC at 0.15 cut-off |
| Single Particle | |
| Number of Projections | 9522 |
| Details | The particles were selected using a semi-automated procedure in spiderspire |
Download | |||
| Data from EMDB | |||
| Header (meta data in XML format) | emd-1737.xml (7.4 KB) | ||
|---|---|---|---|
| Map data | emd_1737.map.gz (5.7 MB) | ||
| Images | EMD1737.jpg (19.5 KB) | ||
| FTP directory | ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1737 | ||
| Movie files | |||
| movie #1 |
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| movie #2 |
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