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Open data
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Basic information
| Entry | Database: PDB / ID: 8hps | |||||||||||||||||||||||||||||||||||||||
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| Title | LpqY-SugABC in state 5 | |||||||||||||||||||||||||||||||||||||||
 Components | 
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 Keywords | TRANSPORT PROTEIN / Trehalose / ABC transporter / tuberculosis | |||||||||||||||||||||||||||||||||||||||
| Function / homology |  Function and homology informationcarbohydrate transport / maltose binding / maltose transport / maltodextrin transmembrane transport / ABC-type transporter activity / ATP-binding cassette (ABC) transporter complex, substrate-binding subunit-containing / transmembrane transport / ATP hydrolysis activity / ATP binding / plasma membrane Similarity search - Function  | |||||||||||||||||||||||||||||||||||||||
| Biological species |  Mycolicibacterium smegmatis MC2 155 (bacteria) | |||||||||||||||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.51 Å | |||||||||||||||||||||||||||||||||||||||
 Authors | Liang, J. / Yang, X. / Zhang, B. / Rao, Z. / Liu, F. | |||||||||||||||||||||||||||||||||||||||
| Funding support |   China, 1items 
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 Citation |  Journal: Structure / Year: 2023Title: Structural insights into trehalose capture and translocation by mycobacterial LpqY-SugABC. Authors: Jingxi Liang / Xiuna Yang / Tianyu Hu / Yan Gao / Qi Yang / Haitao Yang / Wei Peng / Xiaoting Zhou / Luke W Guddat / Bing Zhang / Zihe Rao / Fengjiang Liu /   ![]() Abstract: The human pathogen, Mycobacterium tuberculosis (Mtb) relies heavily on trehalose for both survival and pathogenicity. The type I ATP-binding cassette (ABC) transporter LpqY-SugABC is the only ...The human pathogen, Mycobacterium tuberculosis (Mtb) relies heavily on trehalose for both survival and pathogenicity. The type I ATP-binding cassette (ABC) transporter LpqY-SugABC is the only trehalose import pathway in Mtb. Conformational dynamics of ABC transporters is an important feature to explain how they operate, but experimental structures are determined in a static environment. Therefore, a detailed transport mechanism cannot be elucidated because there is a lack of intermediate structures. Here, we used single-particle cryo-electron microscopy (cryo-EM) to determine the structure of the Mycobacterium smegmatis (M. smegmatis) trehalose-specific importer LpqY-SugABC complex in five different conformations. These structures have been classified and reconstructed from a single cryo-EM dataset. This study allows a comprehensive understanding of the trehalose recycling mechanism in Mycobacteria and also demonstrates the potential of single-particle cryo-EM to explore the dynamic structures of other ABC transporters and molecular machines.  | |||||||||||||||||||||||||||||||||||||||
| History | 
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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 |  8hps.cif.gz | 300.6 KB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb8hps.ent.gz | 238.2 KB | Display |  PDB format | 
| PDBx/mmJSON format |  8hps.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  8hps_validation.pdf.gz | 1.7 MB | Display |  wwPDB validaton report | 
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| Full document |  8hps_full_validation.pdf.gz | 1.8 MB | Display | |
| Data in XML |  8hps_validation.xml.gz | 56.7 KB | Display | |
| Data in CIF |  8hps_validation.cif.gz | 86.7 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/hp/8hps ftp://data.pdbj.org/pub/pdb/validation_reports/hp/8hps | HTTPS FTP  | 
-Related structure data
| Related structure data | ![]() 34942MC ![]() 8hplC ![]() 8hpmC ![]() 8hpnC ![]() 8hprC 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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| 1 | 
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Components
-Protein , 2 types, 2 molecules AE 
| #1: Protein |   Mass: 32739.250 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Mycolicibacterium smegmatis MC2 155 (bacteria)Gene: sugA, MSMEI_4933 Production host:  Mycolicibacterium smegmatis MC2 155 (bacteria)References: UniProt: I7G6S2  | 
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| #4: Protein |   Mass: 50183.086 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Mycolicibacterium smegmatis MC2 155 (bacteria)Gene: MSMEG_5061 Production host:  Mycolicibacterium smegmatis MC2 155 (bacteria)References: UniProt: A0R2C3  | 
-ABC transporter,  ... , 2 types, 3 molecules BCD  
| #2: Protein |   Mass: 29839.441 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Mycolicibacterium smegmatis MC2 155 (bacteria)Gene: MSMEG_5059 Production host:  Mycolicibacterium smegmatis MC2 155 (bacteria)References: UniProt: A0R2C1  | 
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| #3: Protein | Mass: 43702.625 Da / Num. of mol.: 2 / Mutation: E164N Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Mycolicibacterium smegmatis MC2 155 (bacteria)Gene: MSMEG_5058 Production host:  Mycolicibacterium smegmatis MC2 155 (bacteria)References: UniProt: A0R2C0  | 
-Sugars , 1 types, 1 molecules 
| #5: Polysaccharide |  alpha-D-glucopyranose-(1-1)-alpha-D-glucopyranose Source method: isolated from a genetically manipulated source  | 
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-Non-polymers , 2 types, 4 molecules 


| #6: Chemical | | #7: Chemical |  | 
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-Details
| Has ligand of interest | Y | 
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| Has protein modification | N | 
-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: Trehalose-specific importer LpqY-SugABC complex / Type: COMPLEX / Entity ID: #1-#2, #4, #3 / Source: RECOMBINANT | 
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| Source (natural) | Organism:  Mycolicibacterium smegmatis MC2 155 (bacteria) | 
| Source (recombinant) | Organism:  Mycolicibacterium smegmatis MC2 155 (bacteria) | 
| Buffer solution | pH: 7.5 | 
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | 
| Vitrification | Cryogen name: ETHANE | 
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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: FLOOD BEAM | 
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2400 nm / Nominal defocus min: 1200 nm | 
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) | 
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Processing
| EM software | Name: PHENIX / Category: model refinement | ||||||||||||||||||||||||
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.51 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 20723 / Symmetry type: POINT | ||||||||||||||||||||||||
| Refine LS restraints | 
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Mycolicibacterium smegmatis MC2 155 (bacteria)
China, 1items 
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FIELD EMISSION GUN