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Yorodumi- PDB-2lob: PDZ Domain of CAL (Cystic Fibrosis Transmembrane Regulator-Associ... -
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Basic information
| Entry | Database: PDB / ID: 2lob | ||||||
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| Title | PDZ Domain of CAL (Cystic Fibrosis Transmembrane Regulator-Associated Ligand) | ||||||
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Keywords | PEPTIDE BINDING PROTEIN / STRUCTURAL PROTEIN-HYDROLASE complex | ||||||
| Function / homology | Function and homology informationnegative regulation of anion channel activity / positive regulation of voltage-gated chloride channel activity / : / Sec61 translocon complex binding / channel-conductance-controlling ATPase / intracellularly ATP-gated chloride channel activity / positive regulation of enamel mineralization / transepithelial water transport / RHO GTPases regulate CFTR trafficking / negative regulation of protein localization to cell surface ...negative regulation of anion channel activity / positive regulation of voltage-gated chloride channel activity / : / Sec61 translocon complex binding / channel-conductance-controlling ATPase / intracellularly ATP-gated chloride channel activity / positive regulation of enamel mineralization / transepithelial water transport / RHO GTPases regulate CFTR trafficking / negative regulation of protein localization to cell surface / amelogenesis / intracellular pH elevation / chloride channel inhibitor activity / : / Golgi-associated vesicle membrane / trans-Golgi network transport vesicle / multicellular organismal-level water homeostasis / Golgi to plasma membrane transport / cholesterol transport / bicarbonate transport / bicarbonate transmembrane transporter activity / vesicle docking involved in exocytosis / chloride channel regulator activity / membrane hyperpolarization / apical protein localization / chloride transmembrane transporter activity / cholesterol biosynthetic process / sperm capacitation / RHOQ GTPase cycle / chloride channel activity / positive regulation of exocytosis / molecular sequestering activity / ATPase-coupled transmembrane transporter activity / endoplasmic reticulum to Golgi vesicle-mediated transport / positive regulation of insulin secretion involved in cellular response to glucose stimulus / chloride channel complex / ABC-type transporter activity / 14-3-3 protein binding / cellular response to forskolin / chloride transmembrane transport / response to endoplasmic reticulum stress / cellular response to cAMP / PDZ domain binding / establishment of localization in cell / clathrin-coated endocytic vesicle membrane / Defective CFTR causes cystic fibrosis / Late endosomal microautophagy / recycling endosome / ABC-family proteins mediated transport / transmembrane transport / Chaperone Mediated Autophagy / recycling endosome membrane / Aggrephagy / Cargo recognition for clathrin-mediated endocytosis / protein transport / Clathrin-mediated endocytosis / protein-folding chaperone binding / early endosome membrane / transmembrane transporter binding / early endosome / endosome membrane / Ub-specific processing proteases / postsynaptic density / apical plasma membrane / Golgi membrane / lysosomal membrane / dendrite / endoplasmic reticulum membrane / enzyme binding / cell surface / Golgi apparatus / protein-containing complex / ATP hydrolysis activity / ATP binding / identical protein binding / nucleus / membrane / plasma membrane / cytosol / cytoplasm Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | SOLUTION NMR / DGSA-distance geometry simulated annealing | ||||||
| Model details | lowest energy, model 1 | ||||||
Authors | Piserchio, A. / Fellows, A. / Madden, D.R. / Mierke, D.F. | ||||||
Citation | Journal: Biochemistry / Year: 2005Title: Association of the cystic fibrosis transmembrane regulator with CAL: structural features and molecular dynamics. Authors: Piserchio, A. / Fellows, A. / Madden, D.R. / Mierke, D.F. | ||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 2lob.cif.gz | 209 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb2lob.ent.gz | 169 KB | Display | PDB format |
| PDBx/mmJSON format | 2lob.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 2lob_validation.pdf.gz | 419.8 KB | Display | wwPDB validaton report |
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| Full document | 2lob_full_validation.pdf.gz | 552 KB | Display | |
| Data in XML | 2lob_validation.xml.gz | 29.1 KB | Display | |
| Data in CIF | 2lob_validation.cif.gz | 39.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/lo/2lob ftp://data.pdbj.org/pub/pdb/validation_reports/lo/2lob | HTTPS FTP |
-Related structure data
| Similar structure data | |
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| Other databases |
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Links
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Assembly
| Deposited unit | ![]()
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| NMR ensembles |
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Components
| #1: Protein | Mass: 12528.140 Da / Num. of mol.: 1 / Fragment: PDZ domain residues 286-370 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: GOPC, CAL, FIG / Production host: ![]() |
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| #2: Protein/peptide | Mass: 990.046 Da / Num. of mol.: 1 / Fragment: PDZ-binding motif residues 1473-1480 Source method: isolated from a genetically manipulated source Source: (synth.) Homo sapiens (human) / References: UniProt: P13569, EC: 3.6.3.49 |
-Experimental details
-Experiment
| Experiment | Method: SOLUTION NMR | ||||||||||||
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| NMR experiment |
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Sample preparation
| Details | Contents: 1.0 mM [U-100% 13C; U-100% 15N] protein_1, 90% H2O/10% D2O Solvent system: 90% H2O/10% D2O |
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| Sample | Conc.: 1.0 mM / Component: entity_1-1 / Isotopic labeling: [U-100% 13C; U-100% 15N] |
| Sample conditions | Ionic strength: 1 / pH: 6.8 / Pressure: ambient / Temperature: 310 K |
-NMR measurement
| NMR spectrometer | Type: Bruker Avance / Manufacturer: Bruker / Model: AVANCE / Field strength: 600 MHz |
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Processing
| NMR software |
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| Refinement | Method: DGSA-distance geometry simulated annealing / Software ordinal: 1 | |||||||||
| NMR representative | Selection criteria: lowest energy | |||||||||
| NMR ensemble | Conformer selection criteria: structures with the lowest energy Conformers calculated total number: 100 / Conformers submitted total number: 7 |
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Homo sapiens (human)
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