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Open data
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Basic information
| Entry | Database: PDB / ID: 9doq | ||||||||||||||||||||||||||||||
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| Title | Cryo-EM structure of LptB2FGC apo-I | ||||||||||||||||||||||||||||||
Components |
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Keywords | LIPID TRANSPORT / LPS transporter | ||||||||||||||||||||||||||||||
| Function / homology | Function and homology informationlipopolysaccharide transmembrane transporter activity / glycolipid transfer activity / lipopolysaccharide transport / Gram-negative-bacterium-type cell outer membrane assembly / ATP-binding cassette (ABC) transporter complex / transmembrane transport / outer membrane-bounded periplasmic space / ATP hydrolysis activity / ATP binding / plasma membrane / cytoplasm Similarity search - Function | ||||||||||||||||||||||||||||||
| Biological species | ![]() | ||||||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.26 Å | ||||||||||||||||||||||||||||||
Authors | Su, C.C. | ||||||||||||||||||||||||||||||
| Funding support | United States, 1items
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Citation | Journal: To Be PublishedTitle: Structural snapshots of Pseudomonas aeruginosa LptB2FG and LptB2FGC reveal insights into lipopolysaccharide recognition and transport Authors: Su, C. | ||||||||||||||||||||||||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9doq.cif.gz | 271.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9doq.ent.gz | 216.3 KB | Display | PDB format |
| PDBx/mmJSON format | 9doq.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9doq_validation.pdf.gz | 1.7 MB | Display | wwPDB validaton report |
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| Full document | 9doq_full_validation.pdf.gz | 1.7 MB | Display | |
| Data in XML | 9doq_validation.xml.gz | 61.2 KB | Display | |
| Data in CIF | 9doq_validation.cif.gz | 89.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/do/9doq ftp://data.pdbj.org/pub/pdb/validation_reports/do/9doq | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 47088MC ![]() 9dohC ![]() 9dokC ![]() 9dooC ![]() 9dorC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 27833.975 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: lptB_3, lptB, lptB_2, CAZ10_21010, GNQ48_11505, GUL26_13595, IPC1295_15315, IPC737_20870, NCTC13621_04169, PAERUG_P19_London_7_VIM_2_05_10_06438 Production host: ![]() #2: Protein | | Mass: 39511.086 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: lptG, CAZ10_29115, GNQ48_26920, IPC737_18645, NCTC13621_00519 Production host: ![]() #3: Protein | | Mass: 41643.719 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: lptF, CAZ10_29120, DT376_04500, GNQ48_26915, GUL26_00985, IPC1295_13765, IPC737_18640, PAERUG_P19_London_7_VIM_2_05_10_06506 Production host: ![]() #4: Protein | | Mass: 21654.609 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: lptC, ALP65_01219, CAZ10_21020, DT376_04300, GNQ48_11495, GUL26_13585, IPC1295_15325, IPC737_20860, NCTC13621_04171, PAERUG_P19_London_7_VIM_2_05_10_06436 Production host: ![]() #5: Chemical | ChemComp-3PE / Has ligand of interest | N | Has protein modification | N | |
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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 |
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Sample preparation
| Component | Name: LptB2FG / Type: COMPLEX / Entity ID: #1-#4 / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| Specimen | Conc.: 0.5 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES Details: This is from a heterogeneous and impure protein sample. |
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: SPOT SCAN |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2500 nm / Nominal defocus min: 1000 nm |
| Image recording | Electron dose: 29 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
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Processing
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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| 3D reconstruction | Resolution: 3.26 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 83881 / Symmetry type: POINT |
| Atomic model building | Protocol: AB INITIO MODEL |
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FIELD EMISSION GUN