+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-32025 | ||||||||||||
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Title | Structure of SUR2B in complex with MgATP/ADP and P1075 | ||||||||||||
Map data | sharpened map of SUR2B in complex with Mg-nucleotides and P1075 | ||||||||||||
Sample |
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Keywords | SUR2B / ABC transporter / P1075 / MEMBRANE PROTEIN | ||||||||||||
Function / homology | Function and homology information vascular process in circulatory system / substrate-dependent cell migration, cell contraction / oxygen metabolic process / reactive oxygen species biosynthetic process / response to decreased oxygen levels / ATP sensitive Potassium channels / response to peptide / ABC-family proteins mediated transport / inward rectifying potassium channel / sulfonylurea receptor activity ...vascular process in circulatory system / substrate-dependent cell migration, cell contraction / oxygen metabolic process / reactive oxygen species biosynthetic process / response to decreased oxygen levels / ATP sensitive Potassium channels / response to peptide / ABC-family proteins mediated transport / inward rectifying potassium channel / sulfonylurea receptor activity / response to hydrogen sulfide / response to potassium ion / cardiac conduction / circulatory system development / response to oxygen levels / cellular response to potassium ion / coronary vasculature development / ATPase-coupled monoatomic cation transmembrane transporter activity / cellular response to chemical stress / cardiac muscle cell contraction / regulation of potassium ion transmembrane transport / inorganic cation transmembrane transport / blood circulation / syntaxin binding / cellular respiration / response to stress / heterocyclic compound binding / cellular response to ATP / Ion homeostasis / response to ATP / action potential / blood vessel development / potassium ion import across plasma membrane / monoatomic cation transmembrane transport / fatty acid oxidation / ATPase-coupled transmembrane transporter activity / potassium channel activity / ABC-type transporter activity / potassium channel regulator activity / heart morphogenesis / ATP metabolic process / skeletal muscle tissue development / T-tubule / potassium ion transmembrane transport / negative regulation of blood pressure / sarcomere / cellular response to calcium ion / blood vessel diameter maintenance / acrosomal vesicle / regulation of membrane potential / response to activity / mitochondrion organization / potassium ion transport / response to hydrogen peroxide / transmembrane transport / sarcolemma / regulation of blood pressure / response to estrogen / vasodilation / MAPK cascade / cellular response to xenobiotic stimulus / heart development / gene expression / fibroblast proliferation / defense response to virus / transmembrane transporter binding / response to hypoxia / response to xenobiotic stimulus / protein-containing complex binding / negative regulation of apoptotic process / regulation of transcription by RNA polymerase II / ATP hydrolysis activity / protein-containing complex / mitochondrion / ATP binding / identical protein binding / membrane / plasma membrane / cytoplasm Similarity search - Function | ||||||||||||
Biological species | Rattus norvegicus (Norway rat) | ||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.3 Å | ||||||||||||
Authors | Chen L / Ding D | ||||||||||||
Funding support | China, 3 items
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Citation | Journal: Nat Commun / Year: 2022 Title: Structural identification of vasodilator binding sites on the SUR2 subunit. Authors: Dian Ding / Jing-Xiang Wu / Xinli Duan / Songling Ma / Lipeng Lai / Lei Chen / Abstract: ATP-sensitive potassium channels (K), composed of Kir6 and SUR subunits, convert the metabolic status of the cell into electrical signals. Pharmacological activation of SUR2- containing K channels by ...ATP-sensitive potassium channels (K), composed of Kir6 and SUR subunits, convert the metabolic status of the cell into electrical signals. Pharmacological activation of SUR2- containing K channels by class of small molecule drugs known as K openers leads to hyperpolarization of excitable cells and to vasodilation. Thus, K openers could be used to treat cardiovascular diseases. However, where these vasodilators bind to K and how they activate the channel remains elusive. Here, we present cryo-EM structures of SUR2A and SUR2B subunits in complex with Mg-nucleotides and P1075 or levcromakalim, two chemically distinct K openers that are specific to SUR2. Both P1075 and levcromakalim bind to a common site in the transmembrane domain (TMD) of the SUR2 subunit, which is between TMD1 and TMD2 and is embraced by TM10, TM11, TM12, TM14, and TM17. These K openers synergize with Mg-nucleotides to stabilize SUR2 in the NBD-dimerized occluded state to activate the channel. | ||||||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_32025.map.gz | 28.8 MB | EMDB map data format | |
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Header (meta data) | emd-32025-v30.xml emd-32025.xml | 17.3 KB 17.3 KB | Display Display | EMDB header |
Images | emd_32025.png | 95.9 KB | ||
Filedesc metadata | emd-32025.cif.gz | 6.6 KB | ||
Others | emd_32025_half_map_1.map.gz emd_32025_half_map_2.map.gz | 28.3 MB 28.3 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-32025 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-32025 | HTTPS FTP |
-Validation report
Summary document | emd_32025_validation.pdf.gz | 770.3 KB | Display | EMDB validaton report |
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Full document | emd_32025_full_validation.pdf.gz | 769.8 KB | Display | |
Data in XML | emd_32025_validation.xml.gz | 11 KB | Display | |
Data in CIF | emd_32025_validation.cif.gz | 12.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-32025 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-32025 | HTTPS FTP |
-Related structure data
Related structure data | 7vlsMC 7vlrC 7vltC 7vluC 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_32025.map.gz / Format: CCP4 / Size: 30.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | sharpened map of SUR2B in complex with Mg-nucleotides and P1075 | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.314 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: Half-A map of SUR2B in complex with Mg-nucleotides and P1075
File | emd_32025_half_map_1.map | ||||||||||||
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Annotation | Half-A map of SUR2B in complex with Mg-nucleotides and P1075 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half-B map of SUR2B in complex with Mg-nucleotides and P1075
File | emd_32025_half_map_2.map | ||||||||||||
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Annotation | Half-B map of SUR2B in complex with Mg-nucleotides and P1075 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : ATP-binding cassette sub-family C member 9, isoform B
Entire | Name: ATP-binding cassette sub-family C member 9, isoform B |
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Components |
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-Supramolecule #1: ATP-binding cassette sub-family C member 9, isoform B
Supramolecule | Name: ATP-binding cassette sub-family C member 9, isoform B / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: Rattus norvegicus (Norway rat) |
Molecular weight | Theoretical: 174 kDa/nm |
-Macromolecule #1: Isoform SUR2B of ATP-binding cassette sub-family C member 9
Macromolecule | Name: Isoform SUR2B of ATP-binding cassette sub-family C member 9 type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Rattus norvegicus (Norway rat) |
Molecular weight | Theoretical: 174.488562 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: MSLSFCGNNI SSYNIYHGVL QNPCFVDALN LVPHVFLLFI TFPILFIGWG SQSSKVQIHH NTWLHFPGHN LRWILTFALL FVHVCEIAE GIVSDSQRAS RHLHLFMPAV MGFVATTTSI VYYHNIETSN FPKLLLALFL YWVMAFITKT IKLVKYWQLG W GMSDLRFC ...String: MSLSFCGNNI SSYNIYHGVL QNPCFVDALN LVPHVFLLFI TFPILFIGWG SQSSKVQIHH NTWLHFPGHN LRWILTFALL FVHVCEIAE GIVSDSQRAS RHLHLFMPAV MGFVATTTSI VYYHNIETSN FPKLLLALFL YWVMAFITKT IKLVKYWQLG W GMSDLRFC ITGVMVILNG LLMAVEINVI RVRRYVFFMN PQKVKPPEDL QDLGVRFLQP FVNLLSKATY WWMNTLIISA HR KPIDLKA IGKLPIAMRA VTNYVCLKEA YEEQKKKAAD HPNRTPSIWL AMYRAFGRPI LLSSTFRYLA DLLGFAGPLC ISG IVQRVN EPKNNTTRFS ETLSSKEFLE NAHVLAVLLF LALILQRTFL QASYYVTIET GINLRGALLA MIYNKILRLS TSNL SMGEM TLGQINNLVA IETNQLMWFL FLCPNLWAMP VQIIMGVILL YNLLGSSALV GAAVIVLLAP IQYFIATKLA EAQKS TLDY STERLKKTNE ILKGIKLLKL YAWEHIFCKS VEETRMKELS SLKTFALYTS LSIFMNAAIP IAAVLATFVT HAYASG NNL KPAEAFASLS LFHILVTPLF LLSTVVRFAV KAIISVQKLN EFLLSDEIGE DSWRTGEGTL PFESCKKHTG VQSKPIN RK QPGRYHLDNY EQARRLRPAE TEDVAIKVTN GYFSWGSGLA TLSNIDIRIP TGQLTMIVGQ VGCGKSSLLL AILGEMQT L EGKVYWNNVN ESEPSFEATR SRSRYSVAYA AQKPWLLNAT VEENITFGSS FNRQRYKAVT DACSLQPDID LLPFGDQTE IGERGINLSG GQRQRICVAR ALYQNTNIVF LDDPFSALDI HLSDHLMQEG ILKFLQDDKR TVVLVTHKLQ YLTHADWIIA MKDGSVLRE GTLKDIQTKD VELYEHWKTL MNRQDQELEK DMEADQTTLE RKTLRRAMYS REAKAQMEDE DEEEEEEEDE D DNMSTVMR LRTKMPWKTC WWYLTSGGFF LLFLMIFSKL LKHSVIVAID YWLATWTSEY SINDPGKADQ TFYVAGFSIL CG AGIFLCL VTSLTVEWMG LTAAKNLHHN LLNKIILGPI RFFDTTPLGL ILNRFSADTN IIDQHIPPTL ESLTRSTLLC LSA IGMISY ATPVFLIALA PLGVAFYFIQ KYFRVASKDL QELDDSTQLP LLCHFSETAE GLTTIRAFRH ETRFKQRMLE LTDT NNIAY LFLSAANRWL EVRTDYLGAC IVLTASIASI SGSSNSGLVG LGLLYALTIT NYLNWVVRNL ADLEVQMGAV KKVNS FLTM ESENYEGTMD PSQVPEHWPQ EGEIKIHDLC VRYENNLKPV LKHVKAYIKP GQKVGICGRT GSGKSSLSLA FFRMVD IFD GKIVIDGIDI SKLPLHTLRS RLSIILQDPI LFSGSIRFNL DPECKCTDDR LWEALEIAQL KNMVKSLPGG LDATVTE GG ENFSVGQRQL FCLARAFVRK SSILIMDEAT ASIDMATENI LQKVVMTAFA DRTVVTIAHR VHTILTADLV IVMKRGNI L EYDTPESLLA QEDGVFASFV RADM UniProtKB: ATP-binding cassette sub-family C member 9 |
-Macromolecule #2: CHOLESTEROL HEMISUCCINATE
Macromolecule | Name: CHOLESTEROL HEMISUCCINATE / type: ligand / ID: 2 / Number of copies: 1 / Formula: Y01 |
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Molecular weight | Theoretical: 486.726 Da |
Chemical component information | ChemComp-Y01: |
-Macromolecule #3: ADENOSINE-5'-DIPHOSPHATE
Macromolecule | Name: ADENOSINE-5'-DIPHOSPHATE / type: ligand / ID: 3 / Number of copies: 1 / Formula: ADP |
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Molecular weight | Theoretical: 427.201 Da |
Chemical component information | ChemComp-ADP: |
-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 |
-Macromolecule #5: ADENOSINE-5'-TRIPHOSPHATE
Macromolecule | Name: ADENOSINE-5'-TRIPHOSPHATE / type: ligand / ID: 5 / Number of copies: 1 / Formula: ATP |
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Molecular weight | Theoretical: 507.181 Da |
Chemical component information | ChemComp-ATP: |
-Macromolecule #6: 1-cyano-2-(2-methylbutan-2-yl)-3-pyridin-3-yl-guanidine
Macromolecule | Name: 1-cyano-2-(2-methylbutan-2-yl)-3-pyridin-3-yl-guanidine type: ligand / ID: 6 / Number of copies: 1 / Formula: ESV |
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Molecular weight | Theoretical: 231.297 Da |
Chemical component information | ChemComp-ESV: |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 |
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Vitrification | Cryogen name: ETHANE |
-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 / Average electron dose: 52.0 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: 1.8 µm / Nominal defocus min: 1.5 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: OTHER |
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Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 3.3 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC (ver. 3.1.0) / Number images used: 124387 |
Initial angle assignment | Type: OTHER |
Final angle assignment | Type: OTHER |