[English] 日本語
Yorodumi- EMDB-21018: Cryo-EM Structure of the Hyperpolarization-Activated Potassium Ch... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-21018 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | Cryo-EM Structure of the Hyperpolarization-Activated Potassium Channel KAT1: Tetramer | |||||||||
Map data | Structure of the Hyperpolarization-Activated Potassium Channel KAT1: Tetramer | |||||||||
Sample |
| |||||||||
Keywords | membrane protein / voltage-gated ion channel / potassium channel / TRANSPORT PROTEIN | |||||||||
Function / homology | Function and homology information inward rectifier potassium channel activity / monoatomic ion channel complex / identical protein binding / plasma membrane Similarity search - Function | |||||||||
Biological species | Arabidopsis thaliana (thale cress) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.5 Å | |||||||||
Authors | Clark MD / Contreras GF | |||||||||
Funding support | United States, 2 items
| |||||||||
Citation | Journal: Nature / Year: 2020 Title: Electromechanical coupling in the hyperpolarization-activated K channel KAT1. Authors: Michael David Clark / Gustavo F Contreras / Rong Shen / Eduardo Perozo / Abstract: Voltage-gated potassium (K) channels coordinate electrical signalling and control cell volume by gating in response to membrane depolarization or hyperpolarization. However, although voltage-sensing ...Voltage-gated potassium (K) channels coordinate electrical signalling and control cell volume by gating in response to membrane depolarization or hyperpolarization. However, although voltage-sensing domains transduce transmembrane electric field changes by a common mechanism involving the outward or inward translocation of gating charges, the general determinants of channel gating polarity remain poorly understood. Here we suggest a molecular mechanism for electromechanical coupling and gating polarity in non-domain-swapped K channels on the basis of the cryo-electron microscopy structure of KAT1, the hyperpolarization-activated K channel from Arabidopsis thaliana. KAT1 displays a depolarized voltage sensor, which interacts with a closed pore domain directly via two interfaces and indirectly via an intercalated phospholipid. Functional evaluation of KAT1 structure-guided mutants at the sensor-pore interfaces suggests a mechanism in which direct interaction between the sensor and the C-linker hairpin in the adjacent pore subunit is the primary determinant of gating polarity. We suggest that an inward motion of the S4 sensor helix of approximately 5-7 Å can underlie a direct-coupling mechanism, driving a conformational reorientation of the C-linker and ultimately opening the activation gate formed by the S6 intracellular bundle. This direct-coupling mechanism contrasts with allosteric mechanisms proposed for hyperpolarization-activated cyclic nucleotide-gated channels, and may represent an unexpected link between depolarization- and hyperpolarization-activated channels. | |||||||||
History |
|
-Structure visualization
Movie |
Movie viewer |
---|---|
Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_21018.map.gz | 11.2 MB | EMDB map data format | |
---|---|---|---|---|
Header (meta data) | emd-21018-v30.xml emd-21018.xml | 14.5 KB 14.5 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_21018_fsc.xml | 12.1 KB | Display | FSC data file |
Images | emd_21018.png | 65.5 KB | ||
Filedesc metadata | emd-21018.cif.gz | 6.1 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-21018 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-21018 | HTTPS FTP |
-Validation report
Summary document | emd_21018_validation.pdf.gz | 371.7 KB | Display | EMDB validaton report |
---|---|---|---|---|
Full document | emd_21018_full_validation.pdf.gz | 371.2 KB | Display | |
Data in XML | emd_21018_validation.xml.gz | 12.6 KB | Display | |
Data in CIF | emd_21018_validation.cif.gz | 17 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-21018 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-21018 | HTTPS FTP |
-Related structure data
Related structure data | 6v1xMC 6v1yC M: atomic model generated by this map C: citing same article (ref.) |
---|---|
Similar structure data | |
EM raw data | EMPIAR-11054 (Title: Cryo-EM Structure of the Hyperpolarization-Activated Potassium Channel KAT1 Data size: 3.1 TB Data #1: unaligned non-gain-ref movies [micrographs - multiframe]) |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
---|---|
Related items in Molecule of the Month |
-Map
File | Download / File: emd_21018.map.gz / Format: CCP4 / Size: 149.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | Structure of the Hyperpolarization-Activated Potassium Channel KAT1: Tetramer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.064 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-Sample components
-Entire : Hyperpolarization-Activated Potassium Channel KAT1
Entire | Name: Hyperpolarization-Activated Potassium Channel KAT1 |
---|---|
Components |
|
-Supramolecule #1: Hyperpolarization-Activated Potassium Channel KAT1
Supramolecule | Name: Hyperpolarization-Activated Potassium Channel KAT1 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
---|---|
Source (natural) | Organism: Arabidopsis thaliana (thale cress) |
-Macromolecule #1: Potassium channel KAT1
Macromolecule | Name: Potassium channel KAT1 / type: protein_or_peptide / ID: 1 / Number of copies: 4 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: Arabidopsis thaliana (thale cress) |
Molecular weight | Theoretical: 59.639594 KDa |
Recombinant expression | Organism: Spodoptera frugiperda (fall armyworm) |
Sequence | String: MSISWTRNFF ERFCVEEYNI DTIKQSSFLS ADLLPSLGAR INQSTKLRKH IISPFNPRYR AWEMWLVLLV IYSAWICPFQ FAFITYKKD AIFIIDNIVN GFFAIDIILT FFVAYLDSHS YLLVDSPKKI AIRYLSTWFA FDVCSTAPFQ PLSLLFNYNG S ELGFRILS ...String: MSISWTRNFF ERFCVEEYNI DTIKQSSFLS ADLLPSLGAR INQSTKLRKH IISPFNPRYR AWEMWLVLLV IYSAWICPFQ FAFITYKKD AIFIIDNIVN GFFAIDIILT FFVAYLDSHS YLLVDSPKKI AIRYLSTWFA FDVCSTAPFQ PLSLLFNYNG S ELGFRILS MLRLWRLRRV SSLFARLEKD IRFNYFWIRC TKLISVTLFA IHCAGCFNYL IADRYPNPRK TWIGAVYPNF KE ASLWNRY VTALYWSITT LTTTGYGDFH AENPREMLFD IFFMMFNLGL TAYLIGNMTN LVVHWTSRTR TFRDSVRAAS EFA SRNQLP HDIQDQMLSH ICLKFKTEGL KQQETLNNLP KAIRSSIANY LFFPIVHNIY LFQGVSRNFL FQLVSDIDAE YFPP KEDII LQNEAPTDLY ILVSGAVDFT VYVDGHDQFQ GKAVIGETFG EVGVLYYRPQ PFTVRTTELS QILRISRTSL MSAMH AHAD DGRVIMNNLF MKLRGQQSSR GSLEVLFQ UniProtKB: Potassium channel KAT1 |
-Macromolecule #2: (2S)-1-(nonanoyloxy)-3-(phosphonooxy)propan-2-yl tetradecanoate
Macromolecule | Name: (2S)-1-(nonanoyloxy)-3-(phosphonooxy)propan-2-yl tetradecanoate type: ligand / ID: 2 / Number of copies: 4 / Formula: QNP |
---|---|
Molecular weight | Theoretical: 522.652 Da |
Chemical component information | ChemComp-QNP: |
-Macromolecule #3: (3beta,5beta,14beta,17alpha)-cholestan-3-ol
Macromolecule | Name: (3beta,5beta,14beta,17alpha)-cholestan-3-ol / type: ligand / ID: 3 / Number of copies: 4 / Formula: QNJ |
---|---|
Molecular weight | Theoretical: 388.669 Da |
Chemical component information | ChemComp-QNJ: |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 5 mg/mL | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Buffer | pH: 7.4 Component:
| |||||||||||||||
Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 200 / Pretreatment - Type: PLASMA CLEANING / Pretreatment - Time: 30 sec. / Pretreatment - Atmosphere: AIR | |||||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
---|---|
Specialist optics | Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Digitization - Frames/image: 1-40 / Number grids imaged: 1 / Number real images: 1502 / Average exposure time: 12.0 sec. / Average electron dose: 50.0 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: 2.5 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 130000 |
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 |
---|---|
Output model | PDB-6v1x: |