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Yorodumi- PDB-6jb1: Structure of pancreatic ATP-sensitive potassium channel bound wit... -
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Basic information
| Entry | Database: PDB / ID: 6jb1 | |||||||||||||||
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| Title | Structure of pancreatic ATP-sensitive potassium channel bound with repaglinide and ATPgammaS at 3.3A resolution | |||||||||||||||
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Keywords | MEMBRANE PROTEIN / KATP / channel / repaglinide / Kir / ABC transporter / SUR / diabetes / insulin secretagogue | |||||||||||||||
| Function / homology | Function and homology informationATP sensitive Potassium channels / ATP-activated inward rectifier potassium channel activity / glutamate secretion, neurotransmission / response to resveratrol / inward rectifying potassium channel / Regulation of insulin secretion / sulfonylurea receptor activity / ventricular cardiac muscle tissue development / cell body fiber / ABC-family proteins mediated transport ...ATP sensitive Potassium channels / ATP-activated inward rectifier potassium channel activity / glutamate secretion, neurotransmission / response to resveratrol / inward rectifying potassium channel / Regulation of insulin secretion / sulfonylurea receptor activity / ventricular cardiac muscle tissue development / cell body fiber / ABC-family proteins mediated transport / CAMKK-AMPK signaling cascade / voltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential / ATPase-coupled monoatomic cation transmembrane transporter activity / inward rectifier potassium channel activity / Ion homeostasis / : / nervous system process / ankyrin binding / neuromuscular process / response to ATP / response to stress / response to testosterone / potassium ion import across plasma membrane / potassium ion binding / action potential / intercalated disc / axolemma / potassium channel activity / positive regulation of insulin secretion involved in cellular response to glucose stimulus / ABC-type transporter activity / cellular response to nutrient levels / heat shock protein binding / T-tubule / acrosomal vesicle / response to ischemia / determination of adult lifespan / positive regulation of protein localization to plasma membrane / cellular response to glucose stimulus / negative regulation of insulin secretion / ADP binding / cellular response to nicotine / glucose metabolic process / cellular response to tumor necrosis factor / nuclear envelope / response to estradiol / presynapse / presynaptic membrane / transmembrane transporter binding / response to hypoxia / endosome / response to xenobiotic stimulus / neuronal cell body / apoptotic process / glutamatergic synapse / ATP hydrolysis activity / ATP binding / plasma membrane / cytoplasm Similarity search - Function | |||||||||||||||
| Biological species | ![]() Mesocricetus auratus (golden hamster) | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.3 Å | |||||||||||||||
Authors | Chen, L. / Ding, D. / Wang, M. / Wu, J.-X. / Kang, Y. | |||||||||||||||
| Funding support | China, 4items
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Citation | Journal: Cell Rep / Year: 2019Title: The Structural Basis for the Binding of Repaglinide to the Pancreatic K Channel. Authors: Dian Ding / Mengmeng Wang / Jing-Xiang Wu / Yunlu Kang / Lei Chen / ![]() Abstract: Repaglinide (RPG) is a short-acting insulin secretagogue widely prescribed for the treatment of type 2 diabetes. It boosts insulin secretion by inhibiting the pancreatic ATP-sensitive potassium ...Repaglinide (RPG) is a short-acting insulin secretagogue widely prescribed for the treatment of type 2 diabetes. It boosts insulin secretion by inhibiting the pancreatic ATP-sensitive potassium channel (K). However, the mechanisms by which RPG binds to the K channel are poorly understood. Here, we describe two cryo-EM structures: the pancreatic K channel in complex with inhibitory RPG and adenosine-5'-(γ-thio)-triphosphate (ATPγS) at 3.3 Å and a medium-resolution structure of a RPG-bound mini SUR1 protein in which the N terminus of the inward-rectifying potassium channel 6.1 (Kir6.1) is fused to the ABC transporter module of the sulfonylurea receptor 1 (SUR1). These structures reveal the binding site of RPG in the SUR1 subunit. Furthermore, the high-resolution structure reveals the complex architecture of the ATP binding site, which is formed by both Kir6.2 and SUR1 subunits, and the domain-domain interaction interfaces. | |||||||||||||||
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Structure visualization
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| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 6jb1.cif.gz | 1.3 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb6jb1.ent.gz | 1 MB | Display | PDB format |
| PDBx/mmJSON format | 6jb1.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 6jb1_validation.pdf.gz | 3.6 MB | Display | wwPDB validaton report |
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| Full document | 6jb1_full_validation.pdf.gz | 3.8 MB | Display | |
| Data in XML | 6jb1_validation.xml.gz | 194.7 KB | Display | |
| Data in CIF | 6jb1_validation.cif.gz | 272.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/jb/6jb1 ftp://data.pdbj.org/pub/pdb/validation_reports/jb/6jb1 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9787MC ![]() 9788C ![]() 9789C ![]() 6jb3C M: map data used to model this data C: citing same article ( |
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| Similar structure data |
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Assembly
| Deposited unit | ![]()
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Components
-Protein , 2 types, 8 molecules ACEGBDFH
| #1: Protein | Mass: 43615.734 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human) / References: UniProt: Q61743#2: Protein | Mass: 177295.516 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Mesocricetus auratus (golden hamster) / Gene: Abcc8 / Production host: Homo sapiens (human) / References: UniProt: A0A1U7R319 |
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-Non-polymers , 5 types, 68 molecules 








| #3: Chemical | ChemComp-POV / ( #4: Chemical | ChemComp-AGS / #5: Chemical | ChemComp-AJP / #6: Chemical | ChemComp-BJX / #7: Chemical | ChemComp-PTY / |
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-Details
| Has protein modification | Y |
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: KATP / Type: COMPLEX / Entity ID: #1-#2 / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: Homo sapiens (human) |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K2 QUANTUM (4k x 4k) |
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Processing
| EM software | Name: RELION / Version: 2 / Category: 3D reconstruction |
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| CTF correction | Type: NONE |
| Symmetry | Point symmetry: C4 (4 fold cyclic) |
| 3D reconstruction | Resolution: 3.3 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 277548 / Symmetry type: POINT |
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China, 4items
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Homo sapiens (human)
