+
Open data
-
Basic information
| Entry | Database: EMDB / ID: EMD-11784 | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Title | OpuA inhibited inward facing | ||||||||||||
Map data | |||||||||||||
Sample |
| ||||||||||||
Keywords | osmoregulation / ABC-transporter / glycine betaine uptake system / MEMBRANE PROTEIN / cyclic-di-AMP | ||||||||||||
| Function / homology | Function and homology informationABC-type quaternary amine transporter / amine transmembrane transporter activity / ABC-type quaternary ammonium compound transporting activity / carnitine transmembrane transporter activity / glycine betaine transport / choline transport / peptide transport / amino acid transport / ATP-binding cassette (ABC) transporter complex / protein transport ...ABC-type quaternary amine transporter / amine transmembrane transporter activity / ABC-type quaternary ammonium compound transporting activity / carnitine transmembrane transporter activity / glycine betaine transport / choline transport / peptide transport / amino acid transport / ATP-binding cassette (ABC) transporter complex / protein transport / ATP hydrolysis activity / ATP binding / membrane / plasma membrane Similarity search - Function | ||||||||||||
| Biological species | Lactococcus lactis subsp. lactis (lactic acid bacteria) | ||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.1 Å | ||||||||||||
Authors | Sikkema HR / Rheinberger J | ||||||||||||
| Funding support | Netherlands, 3 items
| ||||||||||||
Citation | Journal: Sci Adv / Year: 2020Title: Gating by ionic strength and safety check by cyclic-di-AMP in the ABC transporter OpuA. Authors: Hendrik R Sikkema / Marco van den Noort / Jan Rheinberger / Marijn de Boer / Sabrina T Krepel / Gea K Schuurman-Wolters / Cristina Paulino / Bert Poolman / ![]() Abstract: (Micro)organisms are exposed to fluctuating environmental conditions, and adaptation to stress is essential for survival. Increased osmolality (hypertonicity) causes outflow of water and loss of ...(Micro)organisms are exposed to fluctuating environmental conditions, and adaptation to stress is essential for survival. Increased osmolality (hypertonicity) causes outflow of water and loss of turgor and is dangerous if the cell is not capable of rapidly restoring its volume. The osmoregulatory adenosine triphosphate-binding cassette transporter OpuA restores the cell volume by accumulating large amounts of compatible solute. OpuA is gated by ionic strength and inhibited by the second messenger cyclic-di-AMP, a molecule recently shown to affect many cellular processes. Despite the master regulatory role of cyclic-di-AMP, structural and functional insights into how the second messenger regulates (transport) proteins on the molecular level are lacking. Here, we present high-resolution cryo-electron microscopy structures of OpuA and in vitro activity assays that show how the osmoregulator OpuA is activated by high ionic strength and how cyclic-di-AMP acts as a backstop to prevent unbridled uptake of compatible solutes. | ||||||||||||
| History |
|
-
Structure visualization
| Movie |
Movie viewer |
|---|---|
| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
-
Downloads & links
-EMDB archive
| Map data | emd_11784.map.gz | 59.8 MB | EMDB map data format | |
|---|---|---|---|---|
| Header (meta data) | emd-11784-v30.xml emd-11784.xml | 20.9 KB 20.9 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_11784_fsc.xml | 9.2 KB | Display | FSC data file |
| Images | emd_11784.png | 140.3 KB | ||
| Masks | emd_11784_msk_1.map | 64 MB | Mask map | |
| Filedesc metadata | emd-11784.cif.gz | 6.8 KB | ||
| Others | emd_11784_half_map_1.map.gz emd_11784_half_map_2.map.gz | 48.4 MB 48.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-11784 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-11784 | HTTPS FTP |
-Validation report
| Summary document | emd_11784_validation.pdf.gz | 1 MB | Display | EMDB validaton report |
|---|---|---|---|---|
| Full document | emd_11784_full_validation.pdf.gz | 1 MB | Display | |
| Data in XML | emd_11784_validation.xml.gz | 16 KB | Display | |
| Data in CIF | emd_11784_validation.cif.gz | 21.1 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11784 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11784 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7aheMC ![]() 7ahcC ![]() 7ahdC ![]() 7ahhC C: citing same article ( M: atomic model generated by this map |
|---|---|
| Similar structure data |
-
Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
|---|---|
| Related items in Molecule of the Month |
-
Map
| File | Download / File: emd_11784.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.012 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
-Supplemental data
-Mask #1
| File | emd_11784_msk_1.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-Half map: #1
| File | emd_11784_half_map_1.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-Half map: #2
| File | emd_11784_half_map_2.map | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Projections & Slices |
| ||||||||||||
| Density Histograms |
-
Sample components
-Entire : OpuA inhibited inward facing
| Entire | Name: OpuA inhibited inward facing |
|---|---|
| Components |
|
-Supramolecule #1: OpuA inhibited inward facing
| Supramolecule | Name: OpuA inhibited inward facing / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
|---|---|
| Source (natural) | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) |
-Macromolecule #1: ABC transporter permease subunit
| Macromolecule | Name: ABC transporter permease subunit / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
|---|---|
| Source (natural) | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) |
| Molecular weight | Theoretical: 63.437812 KDa |
| Recombinant expression | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) |
| Sequence | String: MIDLAIGQVP IANWVSSATD WITSTFSSGF DVIQKSGTVL MNGITGALTA VPFWLMIAVV TILAILVSGK KIAFPLFTFI GLSLIANQG LWSDLMSTIT LVLLSSLLSI IIGVPLGIWM AKSDLVAKIV QPILDFMQTM PGFVYLIPAV AFFGIGVVPG V FASVIFAL ...String: MIDLAIGQVP IANWVSSATD WITSTFSSGF DVIQKSGTVL MNGITGALTA VPFWLMIAVV TILAILVSGK KIAFPLFTFI GLSLIANQG LWSDLMSTIT LVLLSSLLSI IIGVPLGIWM AKSDLVAKIV QPILDFMQTM PGFVYLIPAV AFFGIGVVPG V FASVIFAL PPTVRMTNLG IRQVSTELVE AADSFGSTAR QKLFKLEFPL AKGTIMAGVN QTIMLALSMV VIASMIGAPG LG RGVLAAV QSADIGKGFV SGISLVILAI IIDRFTQKLN VSPLEKQGNP TVKKWKRGIA LVSLLALIIG AFSGMSFGKT ASD KKVDLV YMNWDSEVAS INVLTQAMKE HGFDVKTTAL DNAVAWQTVA NGQADGMVSA WLPNTHKTQW QKYGKSVDLL GPNL KGAKV GFVVPSYMNV NSIEDLTNQA NKTITGIEPG AGVMAASEKT LNSYDNLKDW KLVPSSSGAM TVALGEAIKQ HKDIV ITGW SPHWMFNKYD LKYLADPKGT MGTSENINTI VRKGLKKENP EAYKVLDKFN WTTKDMEAVM LDIQNGKTPE EAAKNW IKD HQKEVDKWFK GSIEGRHHHH HH UniProtKB: ABC transporter permease/substrate binding protein |
-Macromolecule #2: ABC-type proline/glycine betaine transport system ATPase component
| Macromolecule | Name: ABC-type proline/glycine betaine transport system ATPase component type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
|---|---|
| Source (natural) | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) |
| Molecular weight | Theoretical: 45.783684 KDa |
| Recombinant expression | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) |
| Sequence | String: MAVKIKIEHL TKIFGKRIKT ALTMVEKGEP KNEILKKTGA TVGVYDTNFE INEGEIFVIM GLSGSGKSTL LRLLNRLIEP TSGKIFIDN QDVATLNKED LLQVRRKTMS MVFQNFGLFP HRTILENTEY GLEVQNVPKE ERRKRAEKAL DNANLLDFKD Q YPKQLSGG ...String: MAVKIKIEHL TKIFGKRIKT ALTMVEKGEP KNEILKKTGA TVGVYDTNFE INEGEIFVIM GLSGSGKSTL LRLLNRLIEP TSGKIFIDN QDVATLNKED LLQVRRKTMS MVFQNFGLFP HRTILENTEY GLEVQNVPKE ERRKRAEKAL DNANLLDFKD Q YPKQLSGG MQQRVGLARA LANDPEILLM DEAFSALDPL IRREMQDELL ELQAKFQKTI IFVSHDLNEA LRIGDRIAIM KD GKIMQIG TGEEILTNPA NDYVKTFVED VDRAKVITAE NIMIPALTTN IDVDGPSVAL KKMKTEEVSS LMAVDKKRQF RGV VTSEQA IAARKNNQPL KDVMTTDVGT VSKEMLVRDI LPIIYDAPTP LAVVDDNGFL KGVLIRGSVL EALADIPDED EVEE IEKEE ENK UniProtKB: Quaternary amine transport ATP-binding protein |
-Macromolecule #3: (2R,3R,3aS,5R,7aR,9R,10R,10aS,12R,14aR)-2,9-bis(6-amino-9H-purin-...
| Macromolecule | Name: (2R,3R,3aS,5R,7aR,9R,10R,10aS,12R,14aR)-2,9-bis(6-amino-9H-purin-9-yl)octahydro-2H,7H-difuro[3,2-d:3',2'-j][1,3,7,9,2,8 ]tetraoxadiphosphacyclododecine-3,5,10,12-tetrol 5,12-dioxide type: ligand / ID: 3 / Number of copies: 1 / Formula: 2BA |
|---|---|
| Molecular weight | Theoretical: 658.412 Da |
-Experimental details
-Structure determination
| Method | cryo EM |
|---|---|
Processing | single particle reconstruction |
| Aggregation state | particle |
-
Sample preparation
| Buffer | pH: 7 Component:
| |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Grid | Model: Quantifoil R1.2/1.3 / Material: GOLD / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 20 sec. / Details: at 5mA | |||||||||
| Vitrification | Cryogen name: ETHANE-PROPANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK IV |
-
Electron microscopy
| Microscope | FEI TALOS ARCTICA |
|---|---|
| Temperature | Min: 90.0 K / Max: 105.0 K |
| Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Digitization - Dimensions - Width: 3838 pixel / Digitization - Dimensions - Height: 3710 pixel / Digitization - Frames/image: 1-60 / Number grids imaged: 1 / Number real images: 1066 / Average exposure time: 9.0 sec. / Average electron dose: 53.0 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 100.0 µm / Calibrated defocus max: 2.0 µm / Calibrated defocus min: 0.5 µm / Calibrated magnification: 49407 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.5 µm / Nominal magnification: 49407 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
+
Image processing
-Atomic model buiding 1
| Refinement | Space: REAL |
|---|---|
| Output model | ![]() PDB-7ahe: |
Movie
Controller
About Yorodumi



Keywords
Lactococcus lactis subsp. lactis (lactic acid bacteria)
Authors
Netherlands, 3 items
Citation
UCSF Chimera


















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















































