+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-44077 | |||||||||
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Title | Human urate transporter 1 URAT1 in apo state | |||||||||
Map data | ||||||||||
Sample |
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Keywords | SLC transporter / SLC22A family / uric acid / inward facing / MEMBRANE PROTEIN | |||||||||
Function / homology | Function and homology information Defective SLC22A12 causes renal hypouricemia 1 (RHUC1) / Organic anion transport / urate transport / renal urate salt excretion / urate metabolic process / urate transmembrane transporter activity / organic anion transport / cellular homeostasis / monoatomic ion transport / PDZ domain binding ...Defective SLC22A12 causes renal hypouricemia 1 (RHUC1) / Organic anion transport / urate transport / renal urate salt excretion / urate metabolic process / urate transmembrane transporter activity / organic anion transport / cellular homeostasis / monoatomic ion transport / PDZ domain binding / brush border membrane / cellular response to insulin stimulus / response to xenobiotic stimulus / apical plasma membrane / extracellular exosome / membrane / plasma membrane Similarity search - Function | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.9 Å | |||||||||
Authors | Dai Y / Lee CH | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Cell Res / Year: 2024 Title: Transport mechanism and structural pharmacology of human urate transporter URAT1. Authors: Yaxin Dai / Chia-Hsueh Lee / Abstract: Urate is an endogenous product of purine metabolism in the liver. High urate levels in the blood lead to gout, a very common and painful inflammatory arthritis. Excreted urate is reabsorbed in the ...Urate is an endogenous product of purine metabolism in the liver. High urate levels in the blood lead to gout, a very common and painful inflammatory arthritis. Excreted urate is reabsorbed in the kidney mainly by URAT1 antiporter, a key target for anti-gout drugs. To uncover the mechanisms of urate transport and drug inhibition, we determined cryo-EM structures of human URAT1 with urate, counter anion pyrazinoate, or anti-gout drugs of different chemotypes - lesinurad, verinurad, and dotinurad. We captured the outward-to-inward transition of URAT1 during urate uptake, revealing that urate binds in a phenylalanine-rich pocket and engages with key gating residues to drive the transport cycle. In contrast to the single binding site for urate, pyrazinoate interacts with three distinct, functionally relevant sites within URAT1, a mechanism that has not yet been observed in other anion antiporters. In addition, we found that while all three drugs compete with substrates and halt the transport cycle, verinurad and dotinurad further hijack gating residues to achieve high potency. These insights advance our understanding of organic anion transport and provide a foundation for designing improved gout therapeutics. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_44077.map.gz | 203.8 MB | EMDB map data format | |
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Header (meta data) | emd-44077-v30.xml emd-44077.xml | 13.5 KB 13.5 KB | Display Display | EMDB header |
Images | emd_44077.png | 84 KB | ||
Filedesc metadata | emd-44077.cif.gz | 5.7 KB | ||
Others | emd_44077_half_map_1.map.gz emd_44077_half_map_2.map.gz | 200.2 MB 200.2 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-44077 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-44077 | HTTPS FTP |
-Validation report
Summary document | emd_44077_validation.pdf.gz | 1.1 MB | Display | EMDB validaton report |
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Full document | emd_44077_full_validation.pdf.gz | 1.1 MB | Display | |
Data in XML | emd_44077_validation.xml.gz | 15.4 KB | Display | |
Data in CIF | emd_44077_validation.cif.gz | 17.9 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-44077 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-44077 | HTTPS FTP |
-Related structure data
Related structure data | 9b1fMC 9b1gC 9b1hC 9b1iC 9b1jC 9b1kC 9b1lC 9b1mC 9b1nC 9b1oC 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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Related items in Molecule of the Month |
-Map
File | Download / File: emd_44077.map.gz / Format: CCP4 / Size: 216 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: 0.649 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_44077_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_44077_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Human Urate transporter 1 in apo state
Entire | Name: Human Urate transporter 1 in apo state |
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Components |
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-Supramolecule #1: Human Urate transporter 1 in apo state
Supramolecule | Name: Human Urate transporter 1 in apo 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 22 member 12
Macromolecule | Name: Solute carrier family 22 member 12 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 59.257402 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: FSELLDLVGG LGRFQVLQTM ALMVSIMWLC TQSMLENFSA AVPSHRCWAP LLDNSTAVST SLSPEALLAI SIPPGPNQRP HQCRRFRQP QWQLLDPNAT ATSWSEADTE PCVDGWVYDR SIFTSTIVAK WNLVCDSHAL KPMAQSIYLA GILVGAAACG P ASDRFGRR ...String: FSELLDLVGG LGRFQVLQTM ALMVSIMWLC TQSMLENFSA AVPSHRCWAP LLDNSTAVST SLSPEALLAI SIPPGPNQRP HQCRRFRQP QWQLLDPNAT ATSWSEADTE PCVDGWVYDR SIFTSTIVAK WNLVCDSHAL KPMAQSIYLA GILVGAAACG P ASDRFGRR LVLTWSYLQM AVMGTAAAFA PAFPVYCLFR FLLAFAVAGV MMNTGTLLME WTAARARPLV MTLNSLGFSF GH GLTAAVA YGVRDWTLLQ LVVSVPFFLC FLYSWWLPES ARWLIIKGKP DQALQELRKV ARINGHKEAK NLTIEVLMSS VKE EVASAK EPRSVLDLFC VPGLRFRTCI STLCWFAFGF TFFGLALDLQ ALGSNIFLLQ MFIGVVDIPA KMGALLLLSH LGRR PTLAA SLLLAGLCIL ANTLVPHEMG ALRSALAVLG LGGVGAAFTC ITIYSSELFP TVLRMTAVGL GQMAARGGAI LGPLV RLLG VHGPWLPLLV YGTVPVLSGL AALLLPETQS LPLPDTIQDV QNQAVKKATH GTLGNSVLKS TQF UniProtKB: Solute carrier family 22 member 12 |
-Macromolecule #2: 2-acetamido-2-deoxy-beta-D-glucopyranose
Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 2 / Number of copies: 1 / Formula: NAG |
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Molecular weight | Theoretical: 221.208 Da |
Chemical component information | ChemComp-NAG: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 6.5 |
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Grid | Model: Quantifoil R1.2/1.3 / Pretreatment - Type: PLASMA CLEANING |
Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 70.8 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: OTHER / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / 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: INSILICO MODEL |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.9 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 328579 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |