+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-24185 | |||||||||
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Title | Structure of AtAtm3 in the outward-facing conformation | |||||||||
Map data | AtAtm3 in the outward-facing conformation | |||||||||
Sample |
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Keywords | ABC transporter / ATPase / MEMBRANE PROTEIN | |||||||||
Function / homology | Function and homology information regulation of chlorophyll biosynthetic process / chloroplast organization / pollen development / root development / regulation of catalytic activity / Mo-molybdopterin cofactor biosynthetic process / chloroplast envelope / plastid / chromosome organization / ABC-type transporter activity ...regulation of chlorophyll biosynthetic process / chloroplast organization / pollen development / root development / regulation of catalytic activity / Mo-molybdopterin cofactor biosynthetic process / chloroplast envelope / plastid / chromosome organization / ABC-type transporter activity / response to cadmium ion / chloroplast / response to lead ion / iron ion transport / intracellular iron ion homeostasis / mitochondrial inner membrane / ATP hydrolysis activity / mitochondrion / ATP binding Similarity search - Function | |||||||||
Biological species | Arabidopsis thaliana (thale cress) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.8 Å | |||||||||
Authors | Fan C / Rees DC | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Elife / Year: 2022 Title: Glutathione binding to the plant Atm3 transporter and implications for the conformational coupling of ABC transporters. Authors: Chengcheng Fan / Douglas C Rees / Abstract: The ATP binding cassette (ABC) transporter of mitochondria (Atm) from (Atm3) has been implicated in the maturation of cytosolic iron-sulfur proteins and heavy metal detoxification, plausibly by ...The ATP binding cassette (ABC) transporter of mitochondria (Atm) from (Atm3) has been implicated in the maturation of cytosolic iron-sulfur proteins and heavy metal detoxification, plausibly by exporting glutathione derivatives. Using single-particle cryo-electron microscopy, we have determined four structures of Atm3 in three different conformational states: two inward-facing conformations (with and without bound oxidized glutathione [GSSG]), together with closed and outward-facing states stabilized by MgADP-VO. These structures not only provide a structural framework for defining the alternating access transport cycle, but also reveal the paucity of cysteine residues in the glutathione binding site that could potentially form inhibitory mixed disulfides with GSSG. Despite extensive efforts, we were unable to prepare the ternary complex of Atm3 containing both GSSG and MgATP. A survey of structurally characterized type IV ABC transporters that includes Atm3 establishes that while nucleotides are found associated with all conformational states, they are effectively required to stabilize occluded, closed, and outward-facing conformations. In contrast, transport substrates have only been observed associated with inward-facing conformations. The absence of structures with dimerized nucleotide binding domains containing both nucleotide and transport substrate suggests that this form of the ternary complex exists only transiently during the transport cycle. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_24185.map.gz | 97.1 MB | EMDB map data format | |
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Header (meta data) | emd-24185-v30.xml emd-24185.xml | 18.2 KB 18.2 KB | Display Display | EMDB header |
Images | emd_24185.png | 90.6 KB | ||
Filedesc metadata | emd-24185.cif.gz | 6.1 KB | ||
Others | emd_24185_half_map_1.map.gz emd_24185_half_map_2.map.gz | 95.3 MB 95.3 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-24185 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-24185 | HTTPS FTP |
-Validation report
Summary document | emd_24185_validation.pdf.gz | 1.2 MB | Display | EMDB validaton report |
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Full document | emd_24185_full_validation.pdf.gz | 1.2 MB | Display | |
Data in XML | emd_24185_validation.xml.gz | 13.4 KB | Display | |
Data in CIF | emd_24185_validation.cif.gz | 15.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-24185 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-24185 | HTTPS FTP |
-Related structure data
Related structure data | 7n5bMC 7n58C 7n59C 7n5aC 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_24185.map.gz / Format: CCP4 / Size: 103 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | AtAtm3 in the outward-facing conformation | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.855 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: AtAtm3 in the outward-facing conformation
File | emd_24185_half_map_1.map | ||||||||||||
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Annotation | AtAtm3 in the outward-facing conformation | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: AtAtm3 in the outward-facing conformation
File | emd_24185_half_map_2.map | ||||||||||||
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Annotation | AtAtm3 in the outward-facing conformation | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : AtAtm3 in detergent
Entire | Name: AtAtm3 in detergent |
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Components |
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-Supramolecule #1: AtAtm3 in detergent
Supramolecule | Name: AtAtm3 in detergent / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: Arabidopsis thaliana (thale cress) |
Molecular weight | Theoretical: 140 KDa |
-Macromolecule #1: ABC transporter B family member 25, mitochondrial
Macromolecule | Name: ABC transporter B family member 25, mitochondrial / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Arabidopsis thaliana (thale cress) |
Molecular weight | Theoretical: 81.793344 KDa |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: MSRGSRFVRA PGLLLCRVNL QPQPKIPSFS YSLRSDYRLH NGFSNYIRRN SIRTSPVINA FLSDNSPSPS PSPSPIRFVQ RSSMLNGRL FSTSTPNPDQ TTTKTKEIKT TSSDSDSAMA DMKILRTLAG YLWMRDNPEF RFRVIAALGF LVGAKVLNVQ V PFLFKLAV ...String: MSRGSRFVRA PGLLLCRVNL QPQPKIPSFS YSLRSDYRLH NGFSNYIRRN SIRTSPVINA FLSDNSPSPS PSPSPIRFVQ RSSMLNGRL FSTSTPNPDQ TTTKTKEIKT TSSDSDSAMA DMKILRTLAG YLWMRDNPEF RFRVIAALGF LVGAKVLNVQ V PFLFKLAV DWLASATGTG ASLTTFAATN PTLLTVFATP AAVLIGYGIA RTGSSAFNEL RTAVFSKVAL RTIRSVSRKV FS HLHDLDL RYHLSRETGG LNRIIDRGSR AINFILSAMV FNVVPTILEI SMVSGILAYK FGAAFAWITS LSVGSYIVFT LAV TQWRTK FRKAMNKADN DASTRAIDSL INYETVKYFN NEGYEAEKYD QFLKKYEDAA LQTQRSLAFL NFGQSIIFST ALST AMVLC SQGIMNGQMT VGDLVMVNGL LFQLSLPLNF LGSVYRETIQ SLVDMKSMFQ LLEEKSDITN TSDAKPLVLK GGNIE FENV HFSYLPERKI LDGISFVVPA GKSVAIVGTS GSGKSTILRM LFRFFDTDSG NIRIDGQDIK EVRLDSLRSS IGVVPQ DTV LFNDTIFHNI HYGRLSATEE EVYEAARRAA IHETISNFPD KYSTIVGERG LKLSGGEKQR VALARTFLKS PAILLCD EA TSALDSTTEA EILNALKALA SNRTSIFIAH RLTTAMQCDE IVVLENGKVV EQGPHDELLG KSGRYAQLWT QQNSSVDM L DAAIKLEAAA LEHHHHHH UniProtKB: ABC transporter B family member 25, mitochondrial |
-Macromolecule #2: ADENOSINE-5'-DIPHOSPHATE
Macromolecule | Name: ADENOSINE-5'-DIPHOSPHATE / type: ligand / ID: 2 / Number of copies: 2 / Formula: ADP |
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Molecular weight | Theoretical: 427.201 Da |
Chemical component information | ChemComp-ADP: |
-Macromolecule #3: VANADATE ION
Macromolecule | Name: VANADATE ION / type: ligand / ID: 3 / Number of copies: 2 / Formula: VO4 |
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Molecular weight | Theoretical: 114.939 Da |
Chemical component information | ChemComp-VN3: |
-Macromolecule #4: MAGNESIUM ION
Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 4 / Number of copies: 2 / Formula: MG |
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Molecular weight | Theoretical: 24.305 Da |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 1 mg/mL | |||||||||
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Buffer | pH: 7.5 Component:
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Grid | Model: UltrAuFoil R1.2/1.3 / Support film - Material: GOLD / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. | |||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Number real images: 5631 / Average exposure time: 2.7 sec. / Average electron dose: 60.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 3.0 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 105000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |