+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-37330 | |||||||||
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Title | NaS1 in IN/IN state | |||||||||
Map data | ||||||||||
Sample |
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Keywords | NaS1 / apo state / IN/IN state / TRANSPORT PROTEIN | |||||||||
Function / homology | Function and homology information sodium:sulfate symporter activity / monoatomic anion:sodium symporter activity / Sodium-coupled sulphate, di- and tri-carboxylate transporters / : / sodium ion transport / transmembrane transport / apical plasma membrane / plasma membrane Similarity search - Function | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.9 Å | |||||||||
Authors | Chi X / Chen Y / Li Y / Zhang Y / Shen Y / Wang Z / Yan R | |||||||||
Funding support | China, 1 items
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Citation | Journal: Sci Adv / Year: 2024 Title: Cryo-EM structures of the human NaS1 and NaDC1 transporters revealed the elevator transport and allosteric regulation mechanism. Authors: Ximin Chi / Yiming Chen / Yaning Li / Lu Dai / Yuanyuan Zhang / Yaping Shen / Yun Chen / Tianhao Shi / Haonan Yang / Zilong Wang / Renhong Yan / Abstract: The solute carrier 13 (SLC13) family comprises electrogenic sodium ion-coupled anion cotransporters, segregating into sodium ion-sulfate cotransporters (NaSs) and sodium ion-di- and-tricarboxylate ...The solute carrier 13 (SLC13) family comprises electrogenic sodium ion-coupled anion cotransporters, segregating into sodium ion-sulfate cotransporters (NaSs) and sodium ion-di- and-tricarboxylate cotransporters (NaDCs). NaS1 and NaDC1 regulate sulfate homeostasis and oxidative metabolism, respectively. NaS1 deficiency affects murine growth and fertility, while NaDC1 affects urinary citrate and calcium nephrolithiasis. Despite their importance, the mechanisms of substrate recognition and transport remain insufficiently characterized. In this study, we determined the cryo-electron microscopy structures of human NaS1, capturing inward-facing and combined inward-facing/outward-facing conformations within a dimer both in apo and sulfate-bound states. In addition, we elucidated NaDC1's outward-facing conformation, encompassing apo, citrate-bound, and -(-amylcinnamoyl) anthranilic acid (ACA) inhibitor-bound states. Structural scrutiny illuminates a detailed elevator mechanism driving conformational changes. Notably, the ACA inhibitor unexpectedly binds primarily anchored by transmembrane 2 (TM2), Loop 10, TM11, and TM6a proximate to the cytosolic membrane. Our findings provide crucial insights into SLC13 transport mechanisms, paving the way for future drug design. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_37330.map.gz | 49.7 MB | EMDB map data format | |
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Header (meta data) | emd-37330-v30.xml emd-37330.xml | 14.5 KB 14.5 KB | Display Display | EMDB header |
Images | emd_37330.png | 90.4 KB | ||
Filedesc metadata | emd-37330.cif.gz | 5.6 KB | ||
Others | emd_37330_half_map_1.map.gz emd_37330_half_map_2.map.gz | 48.5 MB 48.5 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-37330 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-37330 | HTTPS FTP |
-Validation report
Summary document | emd_37330_validation.pdf.gz | 807.2 KB | Display | EMDB validaton report |
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Full document | emd_37330_full_validation.pdf.gz | 806.8 KB | Display | |
Data in XML | emd_37330_validation.xml.gz | 12 KB | Display | |
Data in CIF | emd_37330_validation.cif.gz | 14 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-37330 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-37330 | HTTPS FTP |
-Related structure data
Related structure data | 8w6oMC 8w6cC 8w6dC 8w6gC 8w6hC 8w6nC 8w6tC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_37330.map.gz / Format: CCP4 / Size: 52.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.087 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_37330_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_37330_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Dimer of NaS1 in IN/IN state
Entire | Name: Dimer of NaS1 in IN/IN state |
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Components |
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-Supramolecule #1: Dimer of NaS1 in IN/IN state
Supramolecule | Name: Dimer of NaS1 in IN/IN state / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Solute carrier family 13 member 1
Macromolecule | Name: Solute carrier family 13 member 1 / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 67.68543 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: MADYKDDDDK SGRMKFFSYI LVYRRFLFVV FTVLVLLPLP IVLHTKEAEC AYTLFVVATF WLTEALPLSV TALLPSLMLP MFGIMPSKK VASAYFKDFH LLLIGVICLA TSIEKWNLHK RIALKMVMMV GVNPAWLTLG FMSSTAFLSM WLSNTSTAAM V MPIAEAVV ...String: MADYKDDDDK SGRMKFFSYI LVYRRFLFVV FTVLVLLPLP IVLHTKEAEC AYTLFVVATF WLTEALPLSV TALLPSLMLP MFGIMPSKK VASAYFKDFH LLLIGVICLA TSIEKWNLHK RIALKMVMMV GVNPAWLTLG FMSSTAFLSM WLSNTSTAAM V MPIAEAVV QQIINAEAEV EATQMTYFNG STNHGLEIDE SVNGHEINER KEKTKPVPGY NNDTGKISSK VELEKNSGMR TK YRTKKGH VTRKLTCLCI AYSSTIGGLT TITGTSTNLI FAEYFNTRYP DCRCLNFGSW FTFSFPAALI ILLLSWIWLQ WLF LGFNFK EMFKCGKTKT VQQKACAEVI KQEYQKLGPI RYQEIVTLVL FIIMALLWFS RDPGFVPGWS ALFSEYPGFA TDST VALLI GLLFFLIPAK TLTKTTPTGE IVAFDYSPLI TWKEFQSFMP WDIAILVGGG FALADGCEES GLSKWIGNKL SPLGS LPAW LIILISSLMV TSLTEVASNP ATITLFLPIL SPLAEAIHVN PLYILIPSTL CTSFAFLLPV ANPPNAIVFS YGHLKV IDM VKAGLGVNIV GVAVVMLGIC TWIVPMFDLY TYPSWAPAMS NETMP UniProtKB: Solute carrier family 13 member 1 |
-Macromolecule #2: SODIUM ION
Macromolecule | Name: SODIUM ION / type: ligand / ID: 2 / Number of copies: 4 |
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Molecular weight | Theoretical: 22.99 Da |
-Macromolecule #3: CHOLESTEROL
Macromolecule | Name: CHOLESTEROL / type: ligand / ID: 3 / Number of copies: 2 / Formula: CLR |
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Molecular weight | Theoretical: 386.654 Da |
Chemical component information | ChemComp-CLR: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 8 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: NONE |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.9 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 157920 |
Initial angle assignment | Type: ANGULAR RECONSTITUTION |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |