+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-27856 | |||||||||
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Title | CryoEM structures of bAE1 captured in multiple states. | |||||||||
Map data | ||||||||||
Sample |
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Keywords | cryoEM / Band3 / bAE1 (SLC4A1) / anion exchanger / STRUCTURAL PROTEIN / TRANSPORT PROTEIN | |||||||||
Function / homology | Function and homology information monoatomic anion transmembrane transporter activity / solute:inorganic anion antiporter activity / plasma membrane Similarity search - Function | |||||||||
Biological species | Bos taurus (cattle) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 6.0 Å | |||||||||
Authors | Zhekova HR / Wang WG / Jiang JS / Tsirulnikov K / Muhammad-Khan GH / Azimov R / Abuladze N / Kao L / Newman D / Noskov SY ...Zhekova HR / Wang WG / Jiang JS / Tsirulnikov K / Muhammad-Khan GH / Azimov R / Abuladze N / Kao L / Newman D / Noskov SY / Tieleman P / Zhou ZH / Pushkin A / Kurtz I | |||||||||
Funding support | United States, 2 items
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Citation | Journal: Commun Biol / Year: 2022 Title: CryoEM structures of anion exchanger 1 capture multiple states of inward- and outward-facing conformations. Authors: Hristina R Zhekova / Jiansen Jiang / Weiguang Wang / Kirill Tsirulnikov / Gülru Kayık / Hanif Muhammad Khan / Rustam Azimov / Natalia Abuladze / Liyo Kao / Debbie Newman / Sergei Yu Noskov ...Authors: Hristina R Zhekova / Jiansen Jiang / Weiguang Wang / Kirill Tsirulnikov / Gülru Kayık / Hanif Muhammad Khan / Rustam Azimov / Natalia Abuladze / Liyo Kao / Debbie Newman / Sergei Yu Noskov / D Peter Tieleman / Z Hong Zhou / Alexander Pushkin / Ira Kurtz / Abstract: Anion exchanger 1 (AE1, band 3) is a major membrane protein of red blood cells and plays a key role in acid-base homeostasis, urine acidification, red blood cell shape regulation, and removal of ...Anion exchanger 1 (AE1, band 3) is a major membrane protein of red blood cells and plays a key role in acid-base homeostasis, urine acidification, red blood cell shape regulation, and removal of carbon dioxide during respiration. Though structures of the transmembrane domain (TMD) of three SLC4 transporters, including AE1, have been resolved previously in their outward-facing (OF) state, no mammalian SLC4 structure has been reported in the inward-facing (IF) conformation. Here we present the cryoEM structures of full-length bovine AE1 with its TMD captured in both IF and OF conformations. Remarkably, both IF-IF homodimers and IF-OF heterodimers were detected. The IF structures feature downward movement in the core domain with significant unexpected elongation of TM11. Molecular modeling and structure guided mutagenesis confirmed the functional significance of residues involved in TM11 elongation. Our data provide direct evidence for an elevator-like mechanism of ion transport by an SLC4 family member. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_27856.map.gz | 23.9 MB | EMDB map data format | |
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Header (meta data) | emd-27856-v30.xml emd-27856.xml | 18.4 KB 18.4 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_27856_fsc.xml | 6.7 KB | Display | FSC data file |
Images | emd_27856.png | 84.6 KB | ||
Filedesc metadata | emd-27856.cif.gz | 6.2 KB | ||
Others | emd_27856_half_map_1.map.gz emd_27856_half_map_2.map.gz | 20.4 MB 20.4 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-27856 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-27856 | HTTPS FTP |
-Validation report
Summary document | emd_27856_validation.pdf.gz | 716.9 KB | Display | EMDB validaton report |
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Full document | emd_27856_full_validation.pdf.gz | 716.5 KB | Display | |
Data in XML | emd_27856_validation.xml.gz | 12.5 KB | Display | |
Data in CIF | emd_27856_validation.cif.gz | 17.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-27856 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-27856 | HTTPS FTP |
-Related structure data
Related structure data | 8e34MC 8d9nC 8eeqC 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_27856.map.gz / Format: CCP4 / Size: 27 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: 1.36 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_27856_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_27856_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : band 3 anion transport protein
Entire | Name: band 3 anion transport protein |
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Components |
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-Supramolecule #1: band 3 anion transport protein
Supramolecule | Name: band 3 anion transport protein / type: organelle_or_cellular_component / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Bos taurus (cattle) |
Molecular weight | Theoretical: 104 KDa |
-Macromolecule #1: Anion exchange protein
Macromolecule | Name: Anion exchange protein / type: protein_or_peptide / ID: 1 Details: The cytoplasmic domain was not built because of insufficient resolution. Inward-facing state. Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Bos taurus (cattle) |
Molecular weight | Theoretical: 104.474258 KDa |
Sequence | String: MGDPEEYEDQ LEETLEQKEY EDHDSVSIPM EEAEGDTIQE EEAEARVNQL TDTDYHTTSQ HPETHKVCVQ LRELVMDEKN QEIQWMETA RWVGLEENLG KDGIWGRPHL PYLNFWSLLE LQKAFAKGTV LLDLPGKSLA EVANQLLDRF TFEGQIQPDD Q DNLLRVLL ...String: MGDPEEYEDQ LEETLEQKEY EDHDSVSIPM EEAEGDTIQE EEAEARVNQL TDTDYHTTSQ HPETHKVCVQ LRELVMDEKN QEIQWMETA RWVGLEENLG KDGIWGRPHL PYLNFWSLLE LQKAFAKGTV LLDLPGKSLA EVANQLLDRF TFEGQIQPDD Q DNLLRVLL LKHSHASDME ALGGVKPVVV THSGDPSEPL LPQHPSLETE LFCEQGEGST RGHAPEILGK SPQDWEATLV LV GCARFLK RPVLGFVRLK EPMEPEPKPE GSEEPAVPVR FLIVLLGPEG PNINYTQLGR AAATLMSERV FWNDAYLAQS KET LVQSLE GFLDCSLVLP PLDAPSEKAL LSLVPVQKEL LRRRYLPSPA KPDPSIFKDL DVKKGPGDTP EDPLQRTGKL FGGL VRDIR RRYPRYLSDI TDALSPQVLS AIIFIYFAAL TPAITFGGLL GDKTENMIGV SELLLSTALQ GIIFSLLGAQ PLLVL GFSG PLLVFEEAFY SFCQTNNLEY IVGRVWIGFW LILLVVLVVA FEGSFLVRFI SRYTQEIFSF LISLIFIYET FYKLVT IFQ DHPLQKNYDH DVLTTPKPQA ALPNTALLSL VLMAGTFFLA MMLRKFKNSS YFPGKLRRII GDFGVPISIL IMVMVDA LI QDTYTQKLSV PEGLSVSNPT ERDWLIHPLG IRVEFPIWMM FASALPALLV FILIFLESQI TTLIISKPER KMVKGSGF H LDLLLIIGMG GVGAIFGMPW LSATTVRTVT HANALTVMSK DSTPGAVSQI QGVKEQRISG LLVAVLVGVS ILMGPVLRH IPLAVLFGIF LYMGVTSLSG IQLFDRVLLL LKPRKYYPEV PYARRVKTWR MHLFTITQIV CLVVLWVVRS IKQISLALPF ILILTVPLR RFLLPFIFRD MELKLLDADD VKLNLDEQNG QDEYDEVAMP V UniProtKB: Anion exchange protein |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.4 mg/mL | ||||||||||||
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Buffer | pH: 7.5 Component:
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Vitrification | Cryogen name: NITROGEN / Chamber humidity: 100 % |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Digitization - Frames/image: 1-48 / Average exposure time: 12.0 sec. / Average electron dose: 52.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 50.0 µm / Calibrated magnification: 36764 / Illumination mode: OTHER / Imaging mode: OTHER / Cs: 2.7 mm / Nominal defocus max: 3.2 µm / Nominal defocus min: 1.4000000000000001 µm |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
+Image processing
-Atomic model buiding 1
Refinement | Space: REAL / Protocol: FLEXIBLE FIT |
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Output model | PDB-8e34: |