+Open data
-Basic information
Entry | Database: PDB / ID: 7ahh | ||||||||||||
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Title | OpuA inhibited inward-facing, SBD docked | ||||||||||||
Components |
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Keywords | MEMBRANE PROTEIN / osmoregulation / ABC-transporter / glycine betaine uptake system / cyclic-di-AMP | ||||||||||||
Function / homology | Function and homology information 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 ...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 | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.5 Å | ||||||||||||
Authors | Sikkema, H.R. / Rheinberger, J. / Paulino, C. / Poolman, B. | ||||||||||||
Funding support | Netherlands, 3items
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Citation | Journal: Sci Adv / Year: 2020 Title: 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 |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | Molecule: MolmilJmol/JSmol |
-Downloads & links
-Download
PDBx/mmCIF format | 7ahh.cif.gz | 278.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb7ahh.ent.gz | 221.8 KB | Display | PDB format |
PDBx/mmJSON format | 7ahh.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 7ahh_validation.pdf.gz | 1.5 MB | Display | wwPDB validaton report |
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Full document | 7ahh_full_validation.pdf.gz | 1.5 MB | Display | |
Data in XML | 7ahh_validation.xml.gz | 58.2 KB | Display | |
Data in CIF | 7ahh_validation.cif.gz | 87.1 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ah/7ahh ftp://data.pdbj.org/pub/pdb/validation_reports/ah/7ahh | HTTPS FTP |
-Related structure data
Related structure data | 11786MC 7ahcC 7ahdC 7aheC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
#1: Protein | Mass: 63437.812 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Lactococcus lactis subsp. lactis (lactic acid bacteria) Gene: FEZ45_03205, FIB48_03540, GJI88_00475, GJI90_00975, LL275_1486, N42_0725 Production host: Lactococcus lactis subsp. lactis (lactic acid bacteria) References: UniProt: A0A0V8ETW8 #2: Protein | Mass: 45783.684 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Lactococcus lactis subsp. lactis (lactic acid bacteria) Gene: FEZ45_03200, GJI88_00480, GJI90_00980, KF282_2364, LL275_1487, M20_1239, N42_0726 Production host: Lactococcus lactis subsp. lactis (lactic acid bacteria) References: UniProt: A0A0R2NIU5, UniProt: Q9KIF7*PLUS #3: Chemical | ChemComp-BET / | #4: Chemical | #5: Chemical | ChemComp-2BA / ( | Has ligand of interest | Y | |
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-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component | Name: OpuA inhibited inward-facing, SBD docked / Type: COMPLEX / Entity ID: #1-#2 / Source: RECOMBINANT | |||||||||||||||
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Molecular weight | Experimental value: NO | |||||||||||||||
Source (natural) | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) | |||||||||||||||
Source (recombinant) | Organism: Lactococcus lactis subsp. lactis (lactic acid bacteria) | |||||||||||||||
Buffer solution | pH: 7 | |||||||||||||||
Buffer component |
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Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | |||||||||||||||
Specimen support | Details: at 5 mA / Grid material: GOLD / Grid mesh size: 300 divisions/in. / Grid type: Quantifoil R1.2/1.3 | |||||||||||||||
Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE-PROPANE / Humidity: 100 % / Chamber temperature: 295 K |
-Electron microscopy imaging
Experimental equipment | Model: Talos Arctica / Image courtesy: FEI Company |
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Microscopy | Model: FEI TALOS ARCTICA |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 49407 X / Calibrated magnification: 49407 X / Nominal defocus max: 2000 nm / Nominal defocus min: 500 nm / Calibrated defocus min: 500 nm / Calibrated defocus max: 2000 nm / Cs: 2.7 mm / C2 aperture diameter: 100 µm / Alignment procedure: COMA FREE |
Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Temperature (max): 105 K / Temperature (min): 90 K |
Image recording | Average exposure time: 9 sec. / Electron dose: 53 e/Å2 / Detector mode: COUNTING / Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Num. of grids imaged: 6 / Num. of real images: 7788 |
EM imaging optics | Energyfilter name: GIF Bioquantum / Energyfilter slit width: 20 eV |
Image scans | Width: 3838 / Height: 3710 / Movie frames/image: 60 / Used frames/image: 1-60 |
-Processing
Software | Name: PHENIX / Version: 1.18.2_3874: / Classification: refinement | ||||||||||||||||||||||||
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EM software |
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
Particle selection | Num. of particles selected: 1344075 | ||||||||||||||||||||||||
Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||||||||||
3D reconstruction | Resolution: 3.5 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 110161 / Symmetry type: POINT | ||||||||||||||||||||||||
Atomic model building | Space: REAL | ||||||||||||||||||||||||
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