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Yorodumi- EMDB-7133: Human TRPM4 ion channel in lipid nanodiscs in a calcium-bound state -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-7133 | ||||||||||||||||||
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Title | Human TRPM4 ion channel in lipid nanodiscs in a calcium-bound state | ||||||||||||||||||
Map data | Sharpened map of human TRPM4 ion channel in lipid nanodisc with 5 mM CaCl2. This reconstruction is of the entire molecule with C4 symmetry. | ||||||||||||||||||
Sample |
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Keywords | TRPM4 / TRPM channel / TRP channel / MEMBRANE PROTEIN | ||||||||||||||||||
Function / homology | Function and homology information positive regulation of atrial cardiac muscle cell action potential / positive regulation of regulation of vascular associated smooth muscle cell membrane depolarization / sodium channel complex / regulation of T cell cytokine production / membrane depolarization during AV node cell action potential / membrane depolarization during bundle of His cell action potential / membrane depolarization during Purkinje myocyte cell action potential / negative regulation of bone mineralization / ligand-gated calcium channel activity / sodium ion import across plasma membrane ...positive regulation of atrial cardiac muscle cell action potential / positive regulation of regulation of vascular associated smooth muscle cell membrane depolarization / sodium channel complex / regulation of T cell cytokine production / membrane depolarization during AV node cell action potential / membrane depolarization during bundle of His cell action potential / membrane depolarization during Purkinje myocyte cell action potential / negative regulation of bone mineralization / ligand-gated calcium channel activity / sodium ion import across plasma membrane / regulation of ventricular cardiac muscle cell action potential / calcium-activated cation channel activity / inorganic cation transmembrane transport / TRP channels / dendritic cell chemotaxis / sodium channel activity / cellular response to ATP / positive regulation of heart rate / regulation of heart rate by cardiac conduction / positive regulation of insulin secretion involved in cellular response to glucose stimulus / protein sumoylation / positive regulation of fat cell differentiation / negative regulation of osteoblast differentiation / positive regulation of vasoconstriction / positive regulation of adipose tissue development / calcium-mediated signaling / calcium ion transmembrane transport / Sensory perception of sweet, bitter, and umami (glutamate) taste / positive regulation of canonical Wnt signaling pathway / positive regulation of cytosolic calcium ion concentration / protein homotetramerization / adaptive immune response / calmodulin binding / neuronal cell body / positive regulation of cell population proliferation / calcium ion binding / Golgi apparatus / endoplasmic reticulum / nucleoplasm / ATP binding / identical protein binding / membrane / plasma membrane / cytosol Similarity search - Function | ||||||||||||||||||
Biological species | Homo sapiens (human) | ||||||||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.1 Å | ||||||||||||||||||
Authors | Autzen HE / Myasnikov AG | ||||||||||||||||||
Funding support | United States, Denmark, 5 items
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Citation | Journal: Science / Year: 2018 Title: Structure of the human TRPM4 ion channel in a lipid nanodisc. Authors: Henriette E Autzen / Alexander G Myasnikov / Melody G Campbell / Daniel Asarnow / David Julius / Yifan Cheng / Abstract: Transient receptor potential (TRP) melastatin 4 (TRPM4) is a widely expressed cation channel associated with a variety of cardiovascular disorders. TRPM4 is activated by increased intracellular ...Transient receptor potential (TRP) melastatin 4 (TRPM4) is a widely expressed cation channel associated with a variety of cardiovascular disorders. TRPM4 is activated by increased intracellular calcium in a voltage-dependent manner but, unlike many other TRP channels, is permeable to monovalent cations only. Here we present two structures of full-length human TRPM4 embedded in lipid nanodiscs at ~3-angstrom resolution, as determined by single-particle cryo-electron microscopy. These structures, with and without calcium bound, reveal a general architecture for this major subfamily of TRP channels and a well-defined calcium-binding site within the intracellular side of the S1-S4 domain. The structures correspond to two distinct closed states. Calcium binding induces conformational changes that likely prime the channel for voltage-dependent opening. | ||||||||||||||||||
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_7133.map.gz | 4.2 MB | EMDB map data format | |
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Header (meta data) | emd-7133-v30.xml emd-7133.xml | 27 KB 27 KB | Display Display | EMDB header |
Images | emd_7133.png | 191.2 KB | ||
Filedesc metadata | emd-7133.cif.gz | 6.9 KB | ||
Others | emd_7133_additional_1.map.gz emd_7133_additional_2.map.gz emd_7133_additional_3.map.gz emd_7133_half_map_1.map.gz emd_7133_half_map_2.map.gz | 94.6 MB 2.6 MB 2.5 MB 94.2 MB 94.3 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-7133 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-7133 | HTTPS FTP |
-Validation report
Summary document | emd_7133_validation.pdf.gz | 755.4 KB | Display | EMDB validaton report |
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Full document | emd_7133_full_validation.pdf.gz | 755 KB | Display | |
Data in XML | emd_7133_validation.xml.gz | 14.2 KB | Display | |
Data in CIF | emd_7133_validation.cif.gz | 16.6 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-7133 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-7133 | HTTPS FTP |
-Related structure data
Related structure data | 6bqvMC 7132C 6bqrC C: citing same article (ref.) M: atomic model generated by this map |
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Similar structure data | |
EM raw data | EMPIAR-10127 (Title: Human TRPM4 ion channel in a lipid nanodisc in a calcium-bound state Data size: 84.4 Data #1: particle stacks of TRPM4 particles post 2D clean-up [picked particles - multiframe - processed]) |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_7133.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Sharpened map of human TRPM4 ion channel in lipid nanodisc with 5 mM CaCl2. This reconstruction is of the entire molecule with C4 symmetry. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.046 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Additional map: Unsharpened map of human TRPM4 ion channel in...
File | emd_7133_additional_1.map | ||||||||||||
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Annotation | Unsharpened map of human TRPM4 ion channel in lipid nanodisc with 5 mM CaCl2. This reconstruction is of the entire molecule with C4 symmetry. | ||||||||||||
Projections & Slices |
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Density Histograms |
-Additional map: Sharpened map of human TRPM4 ion channel in...
File | emd_7133_additional_2.map | ||||||||||||
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Annotation | Sharpened map of human TRPM4 ion channel in lipid nanodisc with 5 mM CaCl2. This reconstruction is focused on transmembrane domain, central coiled-coil domain, and MHR4 domain. C4 symmetry is applied. | ||||||||||||
Projections & Slices |
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Density Histograms |
-Additional map: Sharpened map of human TRPM4 ion channel in...
File | emd_7133_additional_3.map | ||||||||||||
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Annotation | Sharpened map of human TRPM4 ion channel in lipid nanodisc with 5 mM CaCl2. This reconstruction is focused on monomeric soluble domain without symmetry. | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Human TRPM4 ion channel in lipid nanodiscs in...
File | emd_7133_half_map_1.map | ||||||||||||
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Annotation | Human TRPM4 ion channel in lipid nanodiscs in a calcium-bound state, half map #1 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half map #2 of human TRPM4 ion channel...
File | emd_7133_half_map_2.map | ||||||||||||
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Annotation | Half map #2 of human TRPM4 ion channel in lipid nanodisc with 5 mM CaCl2. This reconstruction is of the entire molecule with C4 symmetry. | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Human TRPM4 ion channel
Entire | Name: Human TRPM4 ion channel |
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Components |
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-Supramolecule #1: Human TRPM4 ion channel
Supramolecule | Name: Human TRPM4 ion channel / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 Details: Human TRPM4 ion channel in lipid nanodiscs in a calcium-bound state |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 134.6 KDa |
-Macromolecule #1: Transient receptor potential cation channel subfamily M member 4
Macromolecule | Name: Transient receptor potential cation channel subfamily M member 4 type: protein_or_peptide / ID: 1 / Number of copies: 4 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 134.770734 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: SGRSGVVPEK EQSWIPKIFK KKTCTTFIVD STDPGGTLCQ CGRPRTAHPA VAMEDAFGAA VVTVWDSDAH TTEKPTDAYG ELDFTGAGR KHSNFLRLSD RTDPAAVYSL VTRTWGFRAP NLVVSVLGGS GGPVLQTWLQ DLLRRGLVRA AQSTGAWIVT G GLHTGIGR ...String: SGRSGVVPEK EQSWIPKIFK KKTCTTFIVD STDPGGTLCQ CGRPRTAHPA VAMEDAFGAA VVTVWDSDAH TTEKPTDAYG ELDFTGAGR KHSNFLRLSD RTDPAAVYSL VTRTWGFRAP NLVVSVLGGS GGPVLQTWLQ DLLRRGLVRA AQSTGAWIVT G GLHTGIGR HVGVAVRDHQ MASTGGTKVV AMGVAPWGVV RNRDTLINPK GSFPARYRWR GDPEDGVQFP LDYNYSAFFL VD DGTHGCL GGENRFRLRL ESYISQQKTG VGGTGIDIPV LLLLIDGDEK MLTRIENATQ AQLPCLLVAG SGGAADCLAE TLE DTLAPG SGGARQGEAR DRIRRFFPKG DLEVLQAQVE RIMTRKELLT VYSSEDGSEE FETIVLKALV KACGSSEASA YLDE LRLAV AWNRVDIAQS ELFRGDIQWR SFHLEASLMD ALLNDRPEFV RLLISHGLSL GHFLTPMRLA QLYSAAPSNS LIRNL LDQA SHSAGTKAPA LKGGAAELRP PDVGHVLRML LGKMCAPRYP SGGAWDPHPG QGFGESMYLL SDKATSPLSL DAGLGQ APW SDLLLWALLL NRAQMAMYFW EMGSNAVSSA LGACLLLRVM ARLEPDAEEA ARRKDLAFKF EGMGVDLFGE CYRSSEV RA ARLLLRRCPL WGDATCLQLA MQADARAFFA QDGVQSLLTQ KWWGDMASTT PIWALVLAFF CPPLIYTRLI TFRKSEEE P TREELEFDMD SVINGEGPVG TADPAEKTPL GVPRQSGRPG CCGGRCGGRR CLRRWFHFWG APVTIFMGNV VSYLLFLLL FSRVLLVDFQ PAPPGSLELL LYFWAFTLLC EELRQGLSGG GGSLASGGPG PGHASLSQRL RLYLADSWNQ CDLVALTCFL LGVGCRLTP GLYHLGRTVL CIDFMVFTVR LLHIFTVNKQ LGPKIVIVSK MMKDVFFFLF FLGVWLVAYG VATEGLLRPR D SDFPSILR RVFYRPYLQI FGQIPQEDMD VALMEHSNCS SEPGFWAHPP GAQAGTCVSQ YANWLVVLLL VIFLLVANIL LV NLLIAMF SYTFGKVQGN SDLYWKAQRY RLIREFHSRP ALAPPFIVIS HLRLLLRQLC RRPRSPQPSS PALEHFRVYL SKE AERKLL TWESVHKENF LLARARDKRE SDSERLKRTS QKVDLALKQL GHIREYEQRL KVLEREVQQC SRVLGWVAEA LSRS ALLPP GGPPPPDLPG SKD UniProtKB: Transient receptor potential cation channel subfamily M member 4 |
-Macromolecule #2: CALCIUM ION
Macromolecule | Name: CALCIUM ION / type: ligand / ID: 2 / Number of copies: 4 / Formula: CA |
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Molecular weight | Theoretical: 40.078 Da |
-Macromolecule #3: CHOLESTEROL HEMISUCCINATE
Macromolecule | Name: CHOLESTEROL HEMISUCCINATE / type: ligand / ID: 3 / Number of copies: 12 / Formula: Y01 |
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Molecular weight | Theoretical: 486.726 Da |
Chemical component information | ChemComp-Y01: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 2.2 mg/mL | ||||||||||||
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Buffer | pH: 7.4 Component:
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Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY | ||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 283 K / Instrument: FEI VITROBOT MARK IV |
-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 / Number grids imaged: 1 / Number real images: 2954 / Average exposure time: 12.0 sec. / Average electron dose: 62.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.5 µm / Nominal defocus min: 0.5 µm / Nominal magnification: 22500 |
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 | Protocol: AB INITIO MODEL |
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Output model | PDB-6bqv: |