+
Open data
-
Basic information
| Entry | Database: EMDB / ID: EMD-11806 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Title | cryo-EM structure of ExbBD from Serratia Marcescens | |||||||||
Map data | Cryosparc sharpened map | |||||||||
Sample |
| |||||||||
Keywords | TonB transport / MEMBRANE PROTEIN / IRON UPTAKE / PROTON TRANSFER / TONB COMPLEX / METAL TRANSPORT / MOTOR PROTEIN | |||||||||
| Function / homology | Function and homology informationtransmembrane transporter activity / membrane => GO:0016020 / protein transport / plasma membrane Similarity search - Function | |||||||||
| Biological species | Serratia marcescens (bacteria) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.0 Å | |||||||||
Authors | Biou V / Adaixo R | |||||||||
| Funding support | France, 1 items
| |||||||||
Citation | Journal: Commun Biol / Year: 2022Title: Structural and molecular determinants for the interaction of ExbB from Serratia marcescens and HasB, a TonB paralog. Authors: Valérie Biou / Ricardo Jorge Diogo Adaixo / Mohamed Chami / Pierre-Damien Coureux / Benoist Laurent / Véronique Yvette Ntsogo Enguéné / Gisele Cardoso de Amorim / Nadia Izadi-Pruneyre / ...Authors: Valérie Biou / Ricardo Jorge Diogo Adaixo / Mohamed Chami / Pierre-Damien Coureux / Benoist Laurent / Véronique Yvette Ntsogo Enguéné / Gisele Cardoso de Amorim / Nadia Izadi-Pruneyre / Christian Malosse / Julia Chamot-Rooke / Henning Stahlberg / Philippe Delepelaire / ![]() Abstract: ExbB and ExbD are cytoplasmic membrane proteins that associate with TonB to convey the energy of the proton-motive force to outer membrane receptors in Gram-negative bacteria for iron uptake. The ...ExbB and ExbD are cytoplasmic membrane proteins that associate with TonB to convey the energy of the proton-motive force to outer membrane receptors in Gram-negative bacteria for iron uptake. The opportunistic pathogen Serratia marcescens (Sm) possesses both TonB and a heme-specific TonB paralog, HasB. ExbB has a long periplasmic extension absent in other bacteria such as E. coli (Ec). Long ExbB's are found in several genera of Alphaproteobacteria, most often in correlation with a hasB gene. We investigated specificity determinants of ExbB and HasB. We determined the cryo-EM structures of ExbB and of the ExbB-ExbD complex from S. marcescens. ExbB alone is a stable pentamer, and its complex includes two ExbD monomers. We showed that ExbB extension interacts with HasB and is involved in heme acquisition and we identified key residues in the membrane domain of ExbB and ExbB, essential for function and likely involved in the interaction with TonB/HasB. Our results shed light on the class of inner membrane energy machinery formed by ExbB, ExbD and HasB. #1: Journal: Biorxiv / Year: 2021Title: Functional and structural characterization of Serratia marcescens ExbB: determinants of the interaction with HasB/TonB Authors: Biou V / Chami M / Coureux PD / Laurent B / Ntsogo Y / Izadi-Pruneyre N / Malosse C / Chamot-Rooke J / Stahlberg H / Delepelaire P | |||||||||
| History |
|
-
Structure visualization
| Movie |
Movie viewer |
|---|---|
| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
-
Downloads & links
-EMDB archive
| Map data | emd_11806.map.gz | 59.8 MB | EMDB map data format | |
|---|---|---|---|---|
| Header (meta data) | emd-11806-v30.xml emd-11806.xml | 22 KB 22 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_11806_fsc.xml | 9.2 KB | Display | FSC data file |
| Images | emd_11806.png | 66.2 KB | ||
| Filedesc metadata | emd-11806.cif.gz | 6.6 KB | ||
| Others | emd_11806_half_map_1.map.gz emd_11806_half_map_2.map.gz | 59.4 MB 59.4 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-11806 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-11806 | HTTPS FTP |
-Validation report
| Summary document | emd_11806_validation.pdf.gz | 922.1 KB | Display | EMDB validaton report |
|---|---|---|---|---|
| Full document | emd_11806_full_validation.pdf.gz | 921.6 KB | Display | |
| Data in XML | emd_11806_validation.xml.gz | 15.7 KB | Display | |
| Data in CIF | emd_11806_validation.cif.gz | 21 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11806 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11806 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7ajqMC ![]() 6ye4C C: citing same article ( M: atomic model generated by this map |
|---|---|
| Similar structure data |
-
Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
|---|
-
Map
| File | Download / File: emd_11806.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Annotation | Cryosparc sharpened map | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.067 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
-Supplemental data
-Half map: half map B
| File | emd_11806_half_map_1.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Annotation | half map B | ||||||||||||
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-Half map: half map A
| File | emd_11806_half_map_2.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Annotation | half map A | ||||||||||||
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-
Sample components
-Entire : 5-ExbB + 2-ExbD complex
| Entire | Name: 5-ExbB + 2-ExbD complex |
|---|---|
| Components |
|
-Supramolecule #1: 5-ExbB + 2-ExbD complex
| Supramolecule | Name: 5-ExbB + 2-ExbD complex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
|---|---|
| Source (natural) | Organism: Serratia marcescens (bacteria) |
| Molecular weight | Theoretical: 150 KDa |
-Macromolecule #1: Biopolymer transport protein ExbB
| Macromolecule | Name: Biopolymer transport protein ExbB / type: protein_or_peptide / ID: 1 / Number of copies: 5 / Enantiomer: LEVO |
|---|---|
| Source (natural) | Organism: Serratia marcescens (bacteria) |
| Molecular weight | Theoretical: 29.584752 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: APAANPAVTE SVAPTTAPAP AAAAPESITP VNPAPTIQPP ETRGMDLSIW GMYQHADAVV KAVMIGLVLA SIVTWTILFA KGSELLRAK RRLRREQLAL AEARSLDEAS ELAQNFSPES VSAVLLNDAQ NELELSAESN DNNGIKERTG FRLERRVAAY S RNMGRGNG ...String: APAANPAVTE SVAPTTAPAP AAAAPESITP VNPAPTIQPP ETRGMDLSIW GMYQHADAVV KAVMIGLVLA SIVTWTILFA KGSELLRAK RRLRREQLAL AEARSLDEAS ELAQNFSPES VSAVLLNDAQ NELELSAESN DNNGIKERTG FRLERRVAAY S RNMGRGNG FLATIGAISP FVGLFGTVWG IMNSFIGIAH SQTTNLAVVA PGIAEALLAT AMGLVAAIPA VVIYNIFARV IS GHRAQVG DVAAQVLLLQ GRDLDLAATA EAKRSQHAHQ LRAG UniProtKB: Biopolymer transport protein ExbB |
-Macromolecule #2: Biopolymer transport protein ExbD
| Macromolecule | Name: Biopolymer transport protein ExbD / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
|---|---|
| Source (natural) | Organism: Serratia marcescens (bacteria) |
| Molecular weight | Theoretical: 16.26869 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MAMRLNEDLD DSGELHEINV TPFIDVMLVL LIIFMVAAPL ATVDIRVDLP ASSAKPQPRP EKPVFLSVKA DKQLYVGDQP VNADQLTSV LDQRTQANKE TTIFFQADKS VDYETLMSVM DTLRKAGYLK VGLVGMEGAA KHHHHHH UniProtKB: Biopolymer transport protein ExbD |
-Experimental details
-Structure determination
| Method | cryo EM |
|---|---|
Processing | single particle reconstruction |
| Aggregation state | particle |
-
Sample preparation
| Concentration | 0.1 mg/mL | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Buffer | pH: 8 Component:
| ||||||||||||
| Grid | Model: C-flat / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 20 sec. / Pretreatment - Atmosphere: AIR | ||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 293 K / Instrument: FEI VITROBOT MARK II | ||||||||||||
| Details | the sample was monodisperse as seen on gel filtration chromatogram |
-
Electron microscopy
| Microscope | FEI TITAN KRIOS |
|---|---|
| Temperature | Min: 100.0 K / Max: 100.0 K |
| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Digitization - Frames/image: 1-48 / Number grids imaged: 1 / Number real images: 4000 / Average exposure time: 12.0 sec. / Average electron dose: 4.58 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Calibrated defocus max: 2.8000000000000003 µm / Calibrated defocus min: 1.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 139000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
+
Image processing
-Atomic model buiding 1
| Initial model | PDB ID: Chain - Chain ID: A / Chain - Source name: PDB / Chain - Initial model type: experimental model |
|---|---|
| Refinement | Space: REAL / Protocol: RIGID BODY FIT / Overall B value: 169 / Target criteria: correlation coefficient |
| Output model | ![]() PDB-7ajq: |
Movie
Controller
About Yorodumi



Keywords
Serratia marcescens (bacteria)
Authors
France, 1 items
Citation

UCSF Chimera










Z (Sec.)
Y (Row.)
X (Col.)







































