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- PDB-8anh: Structure of the amyloid-forming peptide LYIQWL from Tc5b, grown ... -
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Open data
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Basic information
Entry | Database: PDB / ID: 8anh | ||||||||||||
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Title | Structure of the amyloid-forming peptide LYIQWL from Tc5b, grown from 30% acetonitrile | ||||||||||||
![]() | Peptide LYIQWL from Tc5b | ||||||||||||
![]() | PROTEIN FIBRIL / amyloid | ||||||||||||
Function / homology | ACETONITRILE / trifluoroacetic acid![]() | ||||||||||||
Biological species | synthetic construct (others) | ||||||||||||
Method | ![]() ![]() | ||||||||||||
![]() | Durvanger, Z. | ||||||||||||
Funding support | ![]()
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![]() | ![]() Title: Polymorphic amyloid nanostructures of hormone peptides involved in glucose homeostasis display reversible amyloid formation. Authors: Horvath, D. / Durvanger, Z. / K Menyhard, D. / Sulyok-Eiler, M. / Bencs, F. / Gyulai, G. / Horvath, P. / Taricska, N. / Perczel, A. | ||||||||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 17.9 KB | Display | ![]() |
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PDB format | ![]() | 9 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 395.4 KB | Display | ![]() |
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Full document | ![]() | 395.3 KB | Display | |
Data in XML | ![]() | 2.8 KB | Display | |
Data in CIF | ![]() | 3 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8angC ![]() 8aniC ![]() 8anjC ![]() 8ankC ![]() 8anlC ![]() 8anmC ![]() 8annC ![]() 8onqC C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
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Assembly
Deposited unit | ![]()
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Unit cell |
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Components
#1: Protein/peptide | Mass: 835.001 Da / Num. of mol.: 2 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) |
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#2: Chemical | ChemComp-TFA / |
#3: Chemical | |
#4: Water | ChemComp-HOH / |
Has ligand of interest | N |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 1.52 Å3/Da / Density % sol: 19.31 % |
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Crystal grow | Temperature: 310 K / Method: evaporation, recrystallization Details: Peptide was dissolved in 30% acetonitrile at 0.2 mg/ml concentration and incubated at 310K |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: ![]() |
Detector | Type: RIGAKU HyPix-6000HE / Detector: PIXEL / Date: Sep 7, 2021 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1.54184 Å / Relative weight: 1 |
Reflection | Resolution: 1.25→14.56 Å / Num. obs: 2829 / % possible obs: 99.33 % / Redundancy: 6.6 % / Biso Wilson estimate: 5.88 Å2 / CC1/2: 0.998 / Rrim(I) all: 0.139 / Net I/σ(I): 9.2 |
Reflection shell | Resolution: 1.25→1.29 Å / Mean I/σ(I) obs: 3.1 / Num. unique obs: 284 / CC1/2: 0.777 / Rrim(I) all: 0.468 / % possible all: 97.26 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: ideal 5 residue beta strand form the software Fragon Resolution: 1.25→14.56 Å / SU ML: 0.0842 / Cross valid method: FREE R-VALUE / σ(F): 1.41 / Phase error: 14.1879 Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2
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Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL | ||||||||||||||||||||||||
Displacement parameters | Biso mean: 5.98 Å2 | ||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.25→14.56 Å
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Refine LS restraints |
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LS refinement shell |
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