+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-13597 | |||||||||
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Title | Cryo EM map of bison NHA2 in detergent structure | |||||||||
Map data | ||||||||||
Sample |
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Function / homology | Function and homology information lithium:proton antiporter activity / lithium ion transport / sperm principal piece / sodium ion homeostasis / sodium:proton antiporter activity / sodium ion transport / mitochondrial membrane / recycling endosome / synaptic vesicle membrane / recycling endosome membrane ...lithium:proton antiporter activity / lithium ion transport / sperm principal piece / sodium ion homeostasis / sodium:proton antiporter activity / sodium ion transport / mitochondrial membrane / recycling endosome / synaptic vesicle membrane / recycling endosome membrane / basolateral plasma membrane / endosome membrane / apical plasma membrane / lysosomal membrane / identical protein binding / metal ion binding / plasma membrane Similarity search - Function | |||||||||
Biological species | Bison bison (American bison) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.04 Å | |||||||||
Authors | Matsuoka R / Fudim R / Jung S / Drew D | |||||||||
Funding support | 1 items
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Citation | Journal: Nat Struct Mol Biol / Year: 2022 Title: Structure, mechanism and lipid-mediated remodeling of the mammalian Na/H exchanger NHA2. Authors: Rei Matsuoka / Roman Fudim / Sukkyeong Jung / Chenou Zhang / Andre Bazzone / Yurie Chatzikyriakidou / Carol V Robinson / Norimichi Nomura / So Iwata / Michael Landreh / Laura Orellana / ...Authors: Rei Matsuoka / Roman Fudim / Sukkyeong Jung / Chenou Zhang / Andre Bazzone / Yurie Chatzikyriakidou / Carol V Robinson / Norimichi Nomura / So Iwata / Michael Landreh / Laura Orellana / Oliver Beckstein / David Drew / Abstract: The Na/H exchanger SLC9B2, also known as NHA2, correlates with the long-sought-after Na/Li exchanger linked to the pathogenesis of diabetes mellitus and essential hypertension in humans. Despite the ...The Na/H exchanger SLC9B2, also known as NHA2, correlates with the long-sought-after Na/Li exchanger linked to the pathogenesis of diabetes mellitus and essential hypertension in humans. Despite the functional importance of NHA2, structural information and the molecular basis for its ion-exchange mechanism have been lacking. Here we report the cryo-EM structures of bison NHA2 in detergent and in nanodiscs, at 3.0 and 3.5 Å resolution, respectively. The bison NHA2 structure, together with solid-state membrane-based electrophysiology, establishes the molecular basis for electroneutral ion exchange. NHA2 consists of 14 transmembrane (TM) segments, rather than the 13 TMs previously observed in mammalian Na/H exchangers (NHEs) and related bacterial antiporters. The additional N-terminal helix in NHA2 forms a unique homodimer interface with a large intracellular gap between the protomers, which closes in the presence of phosphoinositol lipids. We propose that the additional N-terminal helix has evolved as a lipid-mediated remodeling switch for the regulation of NHA2 activity. #1: Journal: Nat.Struct.Mol.Biol. / Year: 2022 Title: Structure, mechanism and lipid-mediated remodeling of the mammalian Na+/H+ exchanger NHA2 Authors: Matsuoka R / Fudim F / Jung S / Drew F | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_13597.map.gz | 49.1 MB | EMDB map data format | |
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Header (meta data) | emd-13597-v30.xml emd-13597.xml | 17.4 KB 17.4 KB | Display Display | EMDB header |
Images | emd_13597.png | 65.4 KB | ||
Masks | emd_13597_msk_1.map | 52.7 MB | Mask map | |
Others | emd_13597_half_map_1.map.gz emd_13597_half_map_2.map.gz | 40.8 MB 40.8 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-13597 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-13597 | HTTPS FTP |
-Validation report
Summary document | emd_13597_validation.pdf.gz | 475.3 KB | Display | EMDB validaton report |
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Full document | emd_13597_full_validation.pdf.gz | 474.9 KB | Display | |
Data in XML | emd_13597_validation.xml.gz | 11.4 KB | Display | |
Data in CIF | emd_13597_validation.cif.gz | 13.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-13597 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-13597 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_13597.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: 1.0375 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Mask #1
File | emd_13597_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_13597_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_13597_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : mitochondrial sodium/hydrogen exchanger 9B2
Entire | Name: mitochondrial sodium/hydrogen exchanger 9B2 |
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Components |
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-Supramolecule #1: mitochondrial sodium/hydrogen exchanger 9B2
Supramolecule | Name: mitochondrial sodium/hydrogen exchanger 9B2 / type: organelle_or_cellular_component / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Bison bison (American bison) |
Recombinant expression | Organism: Saccharomyces cerevisiae (brewer's yeast) |
-Macromolecule #1: mitochondrial sodium/hydrogen exchanger 9B2
Macromolecule | Name: mitochondrial sodium/hydrogen exchanger 9B2 / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Bison bison (American bison) |
Recombinant expression | Organism: Saccharomyces cerevisiae (brewer's yeast) |
Sequence | String: MRNQDKRAAH KDSEPSTEVN HTASSYQGRQ QETGMNLRGI DGNEPTEGSN LLNNNEKMQG TPAEPNHLQR RRQIHACPPR GLLARVITN VTMVILLWAV VWSVTGSECL PGGNLFGIIM LFYCAIIGGK LFGLIKLPTL PPLPPLLGML LAGFLIRNVP V ISDNIQIK ...String: MRNQDKRAAH KDSEPSTEVN HTASSYQGRQ QETGMNLRGI DGNEPTEGSN LLNNNEKMQG TPAEPNHLQR RRQIHACPPR GLLARVITN VTMVILLWAV VWSVTGSECL PGGNLFGIIM LFYCAIIGGK LFGLIKLPTL PPLPPLLGML LAGFLIRNVP V ISDNIQIK HKWSSALRSI ALSVILVRAG LGLDSNALKK LKGVCVRLSL GPCLIEACTS AVLAYFLMGL PWQWGFMLGF VL GAVSPAV VVPSMLLLQE GGYGVEKGIP TLLMAAGSFD DILAITGFNT CLGMAFSTGS TVFNVLKGVL EVIIGVVTGL VLG FFIQYF PSSDQDNLVW KRAFLVLGLS VLAVFSSTYF GFPGSGGLCT LVTAFLAGRG WASTKTDVEK VIAVAWDIFQ PLLF GLIGA EVLITALRPE TIGLCVATLG IAVLIRILVT YLMVCFAGFN IKEKIFISFA WLPKATVQAA IGSVALDTAR SHGEK QLEG YGMDVLTVAF LSIIITAPVG SLLIGLLGPR LLQKAEQNKD EEDQGETSIQ V |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 5 mg/mL | ||||||||||||
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Buffer | pH: 8 Component:
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Grid | Model: Quantifoil R2/1 / Material: COPPER / Mesh: 300 | ||||||||||||
Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K2 QUANTUM (4k x 4k) / Detector mode: COUNTING / Digitization - Dimensions - Width: 3838 pixel / Digitization - Dimensions - Height: 3710 pixel / Average electron dose: 80.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |