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Yorodumi- PDB-5aer: Neuronal calcium sensor-1 (NCS-1)from Rattus norvegicus complex w... -
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Basic information
| Entry | Database: PDB / ID: 5aer | |||||||||
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| Title | Neuronal calcium sensor-1 (NCS-1)from Rattus norvegicus complex with D2 dopamine receptor peptide from Homo sapiens | |||||||||
Components |
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Keywords | SIGNALING PROTEIN / NEURONAL CALCIUM SENSOR-1 / DOPAMINE RECEPTOR 2 | |||||||||
| Function / homology | Function and homology informationcalcium-dependent protein kinase inhibitor activity / negative regulation of dopamine receptor signaling pathway / positive regulation of dopamine uptake involved in synaptic transmission / negative regulation of dephosphorylation / positive regulation of glial cell-derived neurotrophic factor production / calcium sensitive guanylate cyclase activator activity / acid secretion / dopamine neurotransmitter receptor activity, coupled via Gi/Go / nervous system process involved in regulation of systemic arterial blood pressure / response to histamine ...calcium-dependent protein kinase inhibitor activity / negative regulation of dopamine receptor signaling pathway / positive regulation of dopamine uptake involved in synaptic transmission / negative regulation of dephosphorylation / positive regulation of glial cell-derived neurotrophic factor production / calcium sensitive guanylate cyclase activator activity / acid secretion / dopamine neurotransmitter receptor activity, coupled via Gi/Go / nervous system process involved in regulation of systemic arterial blood pressure / response to histamine / negative regulation of circadian sleep/wake cycle, sleep / regulation of synapse structural plasticity / regulation of locomotion involved in locomotory behavior / neuron-neuron synaptic transmission / adenohypophysis development / negative regulation of dopamine secretion / positive regulation of renal sodium excretion / negative regulation of cellular response to hypoxia / hyaloid vascular plexus regression / adenylate cyclase-inhibiting dopamine receptor signaling pathway / orbitofrontal cortex development / cerebral cortex GABAergic interneuron migration / response to inactivity / regulation of potassium ion transport / Dopamine receptors / negative regulation of neuron migration / dopamine binding / branching morphogenesis of a nerve / regulation of dopamine uptake involved in synaptic transmission / phospholipase C-activating dopamine receptor signaling pathway / positive regulation of growth hormone secretion / peristalsis / heterotrimeric G-protein binding / drinking behavior / G protein-coupled receptor complex / regulation of presynaptic cytosolic calcium ion concentration / grooming behavior / behavioral response to ethanol / auditory behavior / positive regulation of G protein-coupled receptor signaling pathway / striatum development / dopaminergic synapse / dense core granule / positive regulation of urine volume / positive regulation of multicellular organism growth / G protein-coupled receptor internalization / non-motile cilium / heterocyclic compound binding / negative regulation of synaptic transmission, glutamatergic / response to iron ion / adult walking behavior / arachidonate secretion / response to morphine / ciliary membrane / negative regulation of cytosolic calcium ion concentration / temperature homeostasis / positive regulation of neuroblast proliferation / regulation of synaptic transmission, GABAergic / positive regulation of cytokinesis / pigmentation / regulation of neuron projection development / regulation of synaptic vesicle exocytosis / dopamine metabolic process / dopamine uptake involved in synaptic transmission / regulation of dopamine secretion / cellular response to ethanol / associative learning / response to light stimulus / positive regulation of receptor internalization / positive regulation of exocytosis / lateral plasma membrane / neuroblast proliferation / endocytic vesicle / G-protein alpha-subunit binding / negative regulation of protein secretion / regulation of signal transduction / long-term memory / potassium channel regulator activity / sperm flagellum / prepulse inhibition / postsynaptic cytosol / response to axon injury / postsynaptic modulation of chemical synaptic transmission / voltage-gated calcium channel activity / presynaptic cytosol / synapse assembly / negative regulation of blood pressure / regulation of sodium ion transport / behavioral response to cocaine / cellular response to retinoic acid / release of sequestered calcium ion into cytosol / axon terminus / ionotropic glutamate receptor binding / presynaptic modulation of chemical synaptic transmission / acrosomal vesicle / negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction / positive regulation of calcium-mediated signaling / axonogenesis / regulation of heart rate / negative regulation of innate immune response Similarity search - Function | |||||||||
| Biological species | ![]() HOMO SAPIENS (human) | |||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.19 Å | |||||||||
Authors | Saleem, M. / Karuppiah, V. / Pandalaneni, S. / Burgoyne, R. / Derrick, J.P. / Lian, L.Y. | |||||||||
Citation | Journal: J.Biol.Chem. / Year: 2015Title: Neuronal Calcium Sensor-1 Binds the D2 Dopamine Receptor and G-Protein-Coupled Receptor Kinase 1 (Grk1) Peptides Using Different Modes of Interactions. Authors: Pandalaneni, S. / Karuppiah, V. / Saleem, M. / Haynes, L.P. / Burgoyne, R.D. / Mayans, O. / Derrick, J.P. / Lian, L. | |||||||||
| History |
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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 | 5aer.cif.gz | 99.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb5aer.ent.gz | 77.2 KB | Display | PDB format |
| PDBx/mmJSON format | 5aer.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 5aer_validation.pdf.gz | 437.9 KB | Display | wwPDB validaton report |
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| Full document | 5aer_full_validation.pdf.gz | 438.5 KB | Display | |
| Data in XML | 5aer_validation.xml.gz | 10 KB | Display | |
| Data in CIF | 5aer_validation.cif.gz | 12.8 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ae/5aer ftp://data.pdbj.org/pub/pdb/validation_reports/ae/5aer | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 4yruC ![]() 5aeqC ![]() 5afpC ![]() 1g8iS C: citing same article ( S: Starting model for refinement |
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| Similar structure data |
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Assembly
| Deposited unit | ![]()
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| 1 |
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| Unit cell |
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| Noncrystallographic symmetry (NCS) | NCS oper: (Code: given Matrix: (-0.58, -0.75, 0.3), Vector: |
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Components
| #1: Protein | Mass: 21902.668 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() | ||||||
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| #2: Protein/peptide | Mass: 1720.066 Da / Num. of mol.: 2 / Mutation: YES / Source method: obtained synthetically / Source: (synth.) HOMO SAPIENS (human) / References: UniProt: P14416#3: Chemical | #4: Chemical | ChemComp-K / | #5: Water | ChemComp-HOH / | |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 2.2 Å3/Da / Density % sol: 45 % / Description: NONE |
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-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: Diamond / Beamline: I04-1 / Wavelength: 0.917 |
| Detector | Type: MARRESEARCH MARMOSAIC 300MM / Detector: CCD |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.917 Å / Relative weight: 1 |
| Reflection | Resolution: 2.19→51 Å / Num. obs: 11235 / % possible obs: 97.1 % / Observed criterion σ(I): 2 / Redundancy: 5.4 % / Rmerge(I) obs: 0.07 / Net I/σ(I): 15 |
| Reflection shell | Resolution: 2.19→2.25 Å / Redundancy: 2.8 % / Rmerge(I) obs: 0.5 / Mean I/σ(I) obs: 2.4 / % possible all: 77.8 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: PDB ENTRY 1G8I Resolution: 2.19→51.38 Å / Cor.coef. Fo:Fc: 0.947 / Cor.coef. Fo:Fc free: 0.933 / SU B: 14.902 / SU ML: 0.18 / Cross valid method: THROUGHOUT / ESU R: 0.384 / ESU R Free: 0.247 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS.
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| Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 40.44 Å2
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| Refinement step | Cycle: LAST / Resolution: 2.19→51.38 Å
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HOMO SAPIENS (human)
X-RAY DIFFRACTION
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