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Yorodumi- EMDB-8512: Structure of the human HCN1 hyperpolarization-activated cyclic nu... -
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Basic information
| Entry | Database: EMDB / ID: EMD-8512 | |||||||||
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| Title | Structure of the human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in complex with cAMP | |||||||||
Map data | Human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in complex with cAMP, low-pass filtered to 3.51 A, B-factor sharpened at -120 A2 | |||||||||
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Keywords | pacemaker ion channel / TRANSPORT PROTEIN | |||||||||
| Function / homology | Function and homology informationintracellular cAMP-activated cation channel activity involved in regulation of presynaptic membrane potential / positive regulation of membrane hyperpolarization / HCN channels / general adaptation syndrome, behavioral process / HCN channel complex / retinal cone cell development / intracellularly cAMP-activated cation channel activity / negative regulation of action potential / regulation of SA node cell action potential / regulation of membrane depolarization ...intracellular cAMP-activated cation channel activity involved in regulation of presynaptic membrane potential / positive regulation of membrane hyperpolarization / HCN channels / general adaptation syndrome, behavioral process / HCN channel complex / retinal cone cell development / intracellularly cAMP-activated cation channel activity / negative regulation of action potential / regulation of SA node cell action potential / regulation of membrane depolarization / apical dendrite / maternal behavior / sodium ion import across plasma membrane / negative regulation of synaptic transmission, glutamatergic / response to L-glutamate / apical protein localization / voltage-gated monoatomic cation channel activity / voltage-gated sodium channel activity / potassium ion import across plasma membrane / phosphatidylinositol-3,4,5-trisphosphate binding / regulation of heart rate by cardiac conduction / voltage-gated potassium channel activity / potassium channel activity / neuronal action potential / cAMP binding / cellular response to interferon-beta / presynaptic active zone membrane / phosphatidylinositol-4,5-bisphosphate binding / axon terminus / potassium ion transmembrane transport / dendrite membrane / sodium ion transmembrane transport / cellular response to cAMP / dendritic shaft / regulation of membrane potential / response to calcium ion / protein homotetramerization / basolateral plasma membrane / postsynaptic membrane / axon / neuronal cell body / dendrite / glutamatergic synapse / cell surface / identical protein binding / plasma membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.51 Å | |||||||||
Authors | Lee C-H / MacKinnon R | |||||||||
Citation | Journal: Cell / Year: 2017Title: Structures of the Human HCN1 Hyperpolarization-Activated Channel. Authors: Chia-Hsueh Lee / Roderick MacKinnon / ![]() Abstract: Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels underlie the control of rhythmic activity in cardiac and neuronal pacemaker cells. In HCN, the polarity of voltage dependence is ...Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels underlie the control of rhythmic activity in cardiac and neuronal pacemaker cells. In HCN, the polarity of voltage dependence is uniquely reversed. Intracellular cyclic adenosine monophosphate (cAMP) levels tune the voltage response, enabling sympathetic nerve stimulation to increase the heart rate. We present cryo-electron microscopy structures of the human HCN channel in the absence and presence of cAMP at 3.5 Å resolution. HCN channels contain a K channel selectivity filter-forming sequence from which the amino acids create a unique structure that explains Na and K permeability. The voltage sensor adopts a depolarized conformation, and the pore is closed. An S4 helix of unprecedented length extends into the cytoplasm, contacts the C-linker, and twists the inner helical gate shut. cAMP binding rotates cytoplasmic domains to favor opening of the inner helical gate. These structures advance understanding of ion selectivity, reversed polarity gating, and cAMP regulation in HCN channels. | |||||||||
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Structure visualization
| Movie |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_8512.map.gz | 49.3 MB | EMDB map data format | |
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| Header (meta data) | emd-8512-v30.xml emd-8512.xml | 14 KB 14 KB | Display Display | EMDB header |
| Images | emd_8512.png | 147.3 KB | ||
| Filedesc metadata | emd-8512.cif.gz | 5.6 KB | ||
| Others | emd_8512_additional.map.gz | 37.2 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-8512 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-8512 | HTTPS FTP |
-Validation report
| Summary document | emd_8512_validation.pdf.gz | 589.9 KB | Display | EMDB validaton report |
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| Full document | emd_8512_full_validation.pdf.gz | 589.5 KB | Display | |
| Data in XML | emd_8512_validation.xml.gz | 5.8 KB | Display | |
| Data in CIF | emd_8512_validation.cif.gz | 6.6 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-8512 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-8512 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 5u6pMC ![]() 8511C ![]() 5u6oC C: citing same article ( M: atomic model generated by this map |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_8512.map.gz / Format: CCP4 / Size: 52.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in complex with cAMP, low-pass filtered to 3.51 A, B-factor sharpened at -120 A2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.3 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Additional map: Human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in...
| File | emd_8512_additional.map | ||||||||||||
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| Annotation | Human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in complex with cAMP: unfiltered, unsharpened map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : Human HCN1 hyperpolarization-activated cyclic nucleotide-gated io...
| Entire | Name: Human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in complex with cAMP |
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| Components |
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-Supramolecule #1: Human HCN1 hyperpolarization-activated cyclic nucleotide-gated io...
| Supramolecule | Name: Human HCN1 hyperpolarization-activated cyclic nucleotide-gated ion channel in complex with cAMP type: organelle_or_cellular_component / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Potassium/sodium hyperpolarization-activated cyclic nucleotide-ga...
| Macromolecule | Name: Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 11 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: 74.643734 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MEGGGKPNSS SNSRDDGNSV FPAKASATGA GPAAAEKRLG TPPGGGGAGA KEHGNSVCFK VDGGGGGGGG GGGGEEPAGG FEDAEGPRR QYGFMQRQFT SMLQPGVNKF SLRMFGSQKA VEKEQERVKT AGFWIIHPYS DFRFYWDLIM LIMMVGNLVI I PVGITFFT ...String: MEGGGKPNSS SNSRDDGNSV FPAKASATGA GPAAAEKRLG TPPGGGGAGA KEHGNSVCFK VDGGGGGGGG GGGGEEPAGG FEDAEGPRR QYGFMQRQFT SMLQPGVNKF SLRMFGSQKA VEKEQERVKT AGFWIIHPYS DFRFYWDLIM LIMMVGNLVI I PVGITFFT EQTTTPWIIF NVASDTVFLL DLIMNFRTGT VNEDSSEIIL DPKVIKMNYL KSWFVVDFIS SIPVDYIFLI VE KGMDSEV YKTARALRIV RFTKILSLLR LLRLSRLIRY IHQWEEIFHM TYDLASAVVR IFNLIGMMLL LCHWDGCLQF LVP LLQDFP PDCWVSLNEM VNDSWGKQYS YALFKAMSHM LCIGYGAQAP VSMSDLWITM LSMIVGATCY AMFVGHATAL IQSL DSSRR QYQEKYKQVE QYMSFHKLPA DMRQKIHDYY EHRYQGKIFD EENILNELND PLREEIVNFN CRKLVATMPL FANAD PNFV TAMLSKLRFE VFQPGDYIIR EGAVGKKMYF IQHGVAGVIT KSSKEMKLTD GSYFGEICLL TKGRRTASVR ADTYCR LYS LSVDNFNEVL EEYPMMRRAF ETVAIDRLDR IGKKNSILLQ KFQKDLNTGV FNNQENEILK QIVKHDREMV QAALPRE SS SVLNTDPDAE KPRFASNL UniProtKB: Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1, Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 |
-Macromolecule #2: Potassium/sodium hyperpolarization-activated cyclic nucleotide-ga...
| Macromolecule | Name: Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 11 type: protein_or_peptide / ID: 2 / Number of copies: 4 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 1.635006 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: (UNK)(UNK)(UNK)(UNK)(UNK)(UNK)(UNK)(UNK)(UNK)(UNK) (UNK)(UNK)(UNK)(UNK)(UNK)(UNK) (UNK)(UNK)(UNK) |
-Macromolecule #3: ADENOSINE-3',5'-CYCLIC-MONOPHOSPHATE
| Macromolecule | Name: ADENOSINE-3',5'-CYCLIC-MONOPHOSPHATE / type: ligand / ID: 3 / Number of copies: 4 / Formula: CMP |
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| Molecular weight | Theoretical: 329.206 Da |
| Chemical component information | ![]() ChemComp-CMP: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 5 mg/mL |
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| Buffer | pH: 8 |
| Grid | Model: Quantifoil R1.2/1.3 / Material: GOLD / Mesh: 400 / Pretreatment - Type: GLOW DISCHARGE |
| Vitrification | Cryogen name: ETHANE |
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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: 1.78 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: 3.3000000000000003 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Startup model | Type of model: INSILICO MODEL |
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| Final reconstruction | Applied symmetry - Point group: C4 (4 fold cyclic) / Resolution.type: BY AUTHOR / Resolution: 3.51 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 125339 |
| Initial angle assignment | Type: PROJECTION MATCHING |
| Final angle assignment | Type: PROJECTION MATCHING |
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Homo sapiens (human)
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