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Pyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate

by single particle reconstruction, at 13.2 A resolution

Movie

Orientation:

#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 / IDEM DATA BANK (EMDB) / 1737
TitlePyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate
MapPyruvate carboxylase from S.aureus after addition of acetyl-CoA, AMP-PNP and pyruvate
SamplePyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate
KeywordsPyruvate carboxylase, biotin-dependent carobxylase, acetyl-CoA, multifunctional, pyruvate, oxaloacetate, EC 6.4.1.1, Ligase
AuthorsLasso G, Yu LPC, Gil D, Xiang S, Tong L, Valle M
DateDeposition: 2010-06-01, Header release: 2010-06-11, Map release: 2011-05-19, Last update: 2011-05-19
EMDB SitesEMDB @PDBe (EU), EMDB @RCSB (USA)
Structure Visualization
MoviesMovie 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 viewersYorodumi, 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
ArticleStructure, Vol. 18, Issue 10, Page 1300-10, Year 2010
TitleCryo-EM analysis reveals new insights into the mechanism of action of pyruvate carboxylase.
AuthorsGorka 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.
KeywordsBacterial 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)
LinksPII: S0969-2126(10)00297-2, DOI: 10.1016/j.str.2010.07.008, PubMed: 20947019, PMC: PMC2956116
Map
FileEMD-1737.map ( map file in CCP4 format, 6574 KB )
Projections & SlicesSize of images:
AxesZ (Sec.)Y (Row.)X (Col.)

Surface

Projections

Slices (1/3)

Slices (1/2)

Slices (2/3)

Images are generated by Spider package.

Density
Contour Level:2.65 (by author), 2.65 (movie #1):
Minimum - Maximum: -2.95146 - 9.40166
Average (Standard dev.): 1.30137e-09 (1)
Data TypeImage stored as Reals
Space Group Number1
Map Geometry
Axis orderXYZ
Dimensions118118118
Origin000
Limit117117117
Spacing118118118
Unit CellA= B= C: 332.76 A
Alpha=beta=gamma: 90 degrees
Pixel SpacingX= Y= Z: 2.82 A
CCP4 map header info
modeImage stored as Reals
A/pix X/Y/Z2.822.822.82
M x/y/z118118118
origin x/y/z0.0000.0000.000
length x/y/z332.760332.760332.760
alpha/beta/gamma90.00090.00090.000
start NX/NY/NZ-100-100-100
NX/NY/NZ200200200
MAP C/R/S123
start NC/NR/NS000
NC/NR/NS118118118
start NC,NX/NR,NY/NS,NZ
NC,NX/NR,NY/NS,NZ
D min/max/mean-2.9519.4020.000
Annotation DetailsPyruvate carboxylase from S.aureus after addition of acetyl-CoA, AMP-PNP and pyruvate
Supplement
Images
Images
Sample
NamePyruvate carboxylase from S. aureus after addition of acetyl-CoA, AMP-PNP, KHCO3 and pyruvate
Number of Components1
Oligomeric StateHomotetramer
Theoretical Mass0.52MDa
Component #1: protein - PC
Scientific namePyruvate carboxylase
Common NamePC
Theoretical Mass0.52 MDa
Oligomeric DetailsHomotetramer
Scientific Name of SpeciesStaphylococcus aureus
NCBI taxonomy1280
Recombinant expressionYes
Engineered SourceVector: pET28a
Expression system: Escherichia coli BL21 Star
Experiment
Sample Preparation
Specimen Conc0.1 mg/ml
Specimen Support DetailsQuantifoil R2/2, 100 holey carbon films, cu 200 mesh
Specimen Stateparticle
BufferDetails: 20 mM Tris-HCl, 2mM NaCl, 2mM DTT, 2mM acetyl-CoA, 2mM AMP-PNP, 50 Mm KHCO3, 1m mM pyruvate
pH: 7.5
Vitrification
MethodBlot for 1.5 seconds
Cryogen NameETHANE
Time Resolved State45 sec
DetailsVitrification instrument: Vitrobot (FEI)
Humidity100
InstrumentFEI VITROBOT
Temperature277 Kelvin
Imaging
MicroscopeJEOL 2200FS
Electron Gun
Electron SourceFIELD EMISSION GUN
Accelerating Voltage200 kV
Electron Dose11 e/A**2
Illumination ModeFLOOD BEAM
Lens
MagnificationNominal: 50000
Nominal Cs2 mm
Imaging ModeBRIGHT FIELD
Defocus899 nm - 5544 nm
Energy FilterEnergy Filter: Omega
Specimen Holder
Holdersingle tilt cryoholder
ModelGATAN LIQUID NITROGEN
Temperature99 K
Camera
DetectorKodak film SO-163
Image Acquisition
ScannerZEISS SCAI
Number of Digital Images32
Sampling Size2.82
Processing
Methodsingle particle reconstruction
3D reconstruction
AlgorithmSingle particle
Euler Angles DetailsSpider
SoftwareSpider
CTF CorrectionBy defocus groups (Wiener filter)
Resolution By Author13.2 A
Resolution MethodFSC at 0.15 cut-off
Single Particle
Number of Projections9522
DetailsThe 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 dataemd_1737.map.gz (5.7 MB)
ImagesEMD1737.jpg (19.5 KB)
FTP directoryftp://ftp.pdbj.org/pub/emdb/structures/EMD-1737
Movie files
movie #1
.mp4 (H.264/MPEG-4 AVC format), 3.6 MB
.webm (WebM/VP8 format), 5.4 MB
Session file for UCSF-Chimera, 26.7 KB
movie #2
.mp4 (H.264/MPEG-4 AVC format), 3.2 MB
.webm (WebM/VP8 format), 4.7 MB
Session file for UCSF-Chimera, 26.3 KB