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Yorodumi- EMDB-32460: Composite map of human Kv1.3 channel in dalazatide-bound state wi... -
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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-32460 | |||||||||
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| Title | Composite map of human Kv1.3 channel in dalazatide-bound state with beta subunits | |||||||||
Map data | Composite map generated by combining maps from focused refinement of TM and soluble domains | |||||||||
Sample |
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Keywords | Ion channel / Kv channel / Potassium channel / Peptide toxin / ShK / Dalazatide / Selectivity filter / Molecular dynamics simulation / MEMBRANE PROTEIN | |||||||||
| Function / homology | Function and homology informationpinceau fiber / methylglyoxal reductase (NADPH) (acetol producing) activity / regulation of protein localization to cell surface / voltage-gated monoatomic ion channel activity / : / delayed rectifier potassium channel activity / Voltage gated Potassium channels / Oxidoreductases; Acting on the CH-OH group of donors; With NAD+ or NADP+ as acceptor / juxtaparanode region of axon / regulation of potassium ion transmembrane transport ...pinceau fiber / methylglyoxal reductase (NADPH) (acetol producing) activity / regulation of protein localization to cell surface / voltage-gated monoatomic ion channel activity / : / delayed rectifier potassium channel activity / Voltage gated Potassium channels / Oxidoreductases; Acting on the CH-OH group of donors; With NAD+ or NADP+ as acceptor / juxtaparanode region of axon / regulation of potassium ion transmembrane transport / tertiary granule membrane / action potential / voltage-gated potassium channel activity / potassium channel regulator activity / specific granule membrane / voltage-gated potassium channel complex / potassium ion transmembrane transport / protein homooligomerization / potassium ion transport / cytoplasmic side of plasma membrane / transmembrane transporter binding / cytoskeleton / axon / synapse / Neutrophil degranulation / perinuclear region of cytoplasm / membrane / plasma membrane / cytosol Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.4 Å | |||||||||
Authors | Tyagi A / Ahmed T | |||||||||
| Funding support | Singapore, 1 items
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Citation | Journal: Proc Natl Acad Sci U S A / Year: 2022Title: Rearrangement of a unique Kv1.3 selectivity filter conformation upon binding of a drug. Authors: Anu Tyagi / Tofayel Ahmed / Shi Jian / Saumya Bajaj / Seow Theng Ong / Stephanie Shee Min Goay / Yue Zhao / Igor Vorobyov / Changlin Tian / K George Chandy / Shashi Bhushan / ![]() Abstract: We report two structures of the human voltage-gated potassium channel (Kv) Kv1.3 in immune cells alone (apo-Kv1.3) and bound to an immunomodulatory drug called dalazatide (dalazatide-Kv1.3). Both the ...We report two structures of the human voltage-gated potassium channel (Kv) Kv1.3 in immune cells alone (apo-Kv1.3) and bound to an immunomodulatory drug called dalazatide (dalazatide-Kv1.3). Both the apo-Kv1.3 and dalazatide-Kv1.3 structures are in an activated state based on their depolarized voltage sensor and open inner gate. In apo-Kv1.3, the aromatic residue in the signature sequence (Y447) adopts a position that diverges 11 Å from other K channels. The outer pore is significantly rearranged, causing widening of the selectivity filter and perturbation of ion binding within the filter. This conformation is stabilized by a network of intrasubunit hydrogen bonds. In dalazatide-Kv1.3, binding of dalazatide to the channel's outer vestibule narrows the selectivity filter, Y447 occupies a position seen in other K channels, and this conformation is stabilized by a network of intersubunit hydrogen bonds. These remarkable rearrangements in the selectivity filter underlie Kv1.3's transition into the drug-blocked state. | |||||||||
| History |
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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_32460.map.gz | 21.7 MB | EMDB map data format | |
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| Header (meta data) | emd-32460-v30.xml emd-32460.xml | 14.5 KB 14.5 KB | Display Display | EMDB header |
| Images | emd_32460.png | 128.4 KB | ||
| Filedesc metadata | emd-32460.cif.gz | 6 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-32460 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-32460 | HTTPS FTP |
-Validation report
| Summary document | emd_32460_validation.pdf.gz | 357.6 KB | Display | EMDB validaton report |
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| Full document | emd_32460_full_validation.pdf.gz | 357.2 KB | Display | |
| Data in XML | emd_32460_validation.xml.gz | 7.7 KB | Display | |
| Data in CIF | emd_32460_validation.cif.gz | 8.9 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-32460 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-32460 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7wf4MC ![]() 7wf3C M: atomic model generated by this map C: citing same article ( |
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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_32460.map.gz / Format: CCP4 / Size: 282.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Composite map generated by combining maps from focused refinement of TM and soluble domains | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.858 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : Composite map of human Kv1.3 channel in dalazatide-bound state wi...
| Entire | Name: Composite map of human Kv1.3 channel in dalazatide-bound state with beta subunits |
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| Components |
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-Supramolecule #1: Composite map of human Kv1.3 channel in dalazatide-bound state wi...
| Supramolecule | Name: Composite map of human Kv1.3 channel in dalazatide-bound state with beta subunits type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3 |
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-Supramolecule #2: TM domain focused map of human Kv1.3 channel bound to dalazatide
| Supramolecule | Name: TM domain focused map of human Kv1.3 channel bound to dalazatide type: complex / ID: 2 / Parent: 1 / Macromolecule list: #2 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Supramolecule #3: Focused map of human Kv1.3 channel T1 domains and beta 2.1 subunits
| Supramolecule | Name: Focused map of human Kv1.3 channel T1 domains and beta 2.1 subunits type: complex / ID: 3 / Parent: 1 / Macromolecule list: #1, #3 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Potassium voltage-gated channel subfamily A member 3
| Macromolecule | Name: Potassium voltage-gated channel subfamily A member 3 / 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: 31.460467 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: ERPLPRRDFQ RQVWLLFEYP ESSGPARGIA IVSVLVILIS IVIFCLETLP EFRDEKDYPA STSQDSFEAA GNSTSGSRAG ASSFSDPFF VVETLCIIWF SFELLVRFFA CPSKATFSRN IMNLIDIVAI IPYFITLGTE LAERQGNGQQ AMSLAILRVI R LVRVFRIF ...String: ERPLPRRDFQ RQVWLLFEYP ESSGPARGIA IVSVLVILIS IVIFCLETLP EFRDEKDYPA STSQDSFEAA GNSTSGSRAG ASSFSDPFF VVETLCIIWF SFELLVRFFA CPSKATFSRN IMNLIDIVAI IPYFITLGTE LAERQGNGQQ AMSLAILRVI R LVRVFRIF KLSRHSKGLQ ILGQTLKASM RELGLLIFFL FIGVILFSSA VYFAEADDPT SGFSSIPDAF WWAVVTMTTV GY GDMHPVT IGGKIVGSLC AIAGVLTIAL PVPVIVSNFN YFYHRE UniProtKB: Potassium voltage-gated channel subfamily A member 3 |
-Macromolecule #2: Voltage-gated potassium channel subunit beta-2
| Macromolecule | Name: Voltage-gated potassium channel subunit beta-2 / type: protein_or_peptide / ID: 2 / Number of copies: 4 / Enantiomer: LEVO EC number: Oxidoreductases; Acting on the CH-OH group of donors; With NAD+ or NADP+ as acceptor |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 36.704254 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: RQLQFYRNLG KSGLRVSCLG LGTWVTFGGQ ITDEMAEQLM TLAYDNGINL FDTAEVYAAG KAEVVLGNII KKKGWRRSSL VITTKIFWG GKAETERGLS RKHIIEGLKA SLERLQLEYV DVVFANRPDP NTPMEETVRA MTHVINQGMA MYWGTSRWSS M EIMEAYSV ...String: RQLQFYRNLG KSGLRVSCLG LGTWVTFGGQ ITDEMAEQLM TLAYDNGINL FDTAEVYAAG KAEVVLGNII KKKGWRRSSL VITTKIFWG GKAETERGLS RKHIIEGLKA SLERLQLEYV DVVFANRPDP NTPMEETVRA MTHVINQGMA MYWGTSRWSS M EIMEAYSV ARQFNLTPPI CEQAEYHMFQ REKVEVQLPE LFHKIGVGAM TWSPLACGIV SGKYDSGIPP YSRASLKGYQ WL KDKILSE EGRRQQAKLK ELQAIAERLG CTLPQLAIAW CLRNEGVSSV LLGASNADQL MENIGAIQVL PKLSSSIIHE IDS ILGNKP YS UniProtKB: Voltage-gated potassium channel subunit beta-2 |
-Macromolecule #3: Potassium voltage-gated channel subfamily A member 3
| Macromolecule | Name: Potassium voltage-gated channel subfamily A member 3 / type: protein_or_peptide / ID: 3 / Number of copies: 4 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 12.777475 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: QDCCGERVVI NISGLRFETQ LKTLCQFPET LLGDPKRRMR YFDPLRNEYF FDRNRPSFDA ILYYYQSGGR IRRPVNVPID IFSEEIRFY QLGEEAMEKF REDEGFL UniProtKB: Potassium voltage-gated channel subfamily A member 3 |
-Macromolecule #4: NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
| Macromolecule | Name: NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE / type: ligand / ID: 4 / Number of copies: 4 / Formula: NAP |
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| Molecular weight | Theoretical: 743.405 Da |
| Chemical component information | ![]() ChemComp-NAP: |
-Macromolecule #5: POTASSIUM ION
| Macromolecule | Name: POTASSIUM ION / type: ligand / ID: 5 / Number of copies: 3 / Formula: K |
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| Molecular weight | Theoretical: 39.098 Da |
-Macromolecule #6: water
| Macromolecule | Name: water / type: ligand / ID: 6 / Number of copies: 100 / Formula: HOH |
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| Molecular weight | Theoretical: 18.015 Da |
| Chemical component information | ![]() ChemComp-HOH: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.5 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 65.0 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: 2.5 µm / Nominal defocus min: 1.0 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 | Resolution.type: BY AUTHOR / Resolution: 3.4 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 153218 |
| Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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Keywords
Homo sapiens (human)
Authors
Singapore, 1 items
Citation

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