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- PDB-7zqi: MHC class I from a wild bird in complex with a nonameric peptide P2 -
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Open data
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Basic information
Entry | Database: PDB / ID: 7zqi | ||||||
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Title | MHC class I from a wild bird in complex with a nonameric peptide P2 | ||||||
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![]() | IMMUNE SYSTEM / Major Histocompatibility Complex Class I / Acrocephalus arundinaceus / antigen presentation / cell-surface receptor / nonameric peptide from Vibrio | ||||||
Function / homology | ![]() antigen processing and presentation of peptide antigen via MHC class I / lumenal side of endoplasmic reticulum membrane / MHC class I protein complex / phagocytic vesicle membrane / immune response / external side of plasma membrane / extracellular space / extracellular region / metal ion binding Similarity search - Function | ||||||
Biological species | ![]() ![]() | ||||||
Method | ![]() ![]() ![]() | ||||||
![]() | Eltschkner, S. / Mellinger, S. / Buus, S. / Nielsen, M. / Paulsson, K.M. / Lindkvist-Petersson, K. / Westerdahl, H. | ||||||
Funding support | European Union, 1items
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![]() | ![]() Title: The structure of songbird MHC class I reveals antigen binding that is flexible at the N-terminus and static at the C-terminus. Authors: Eltschkner, S. / Mellinger, S. / Buus, S. / Nielsen, M. / Paulsson, K.M. / Lindkvist-Petersson, K. / Westerdahl, H. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 182.8 KB | Display | ![]() |
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PDB format | ![]() | 143.8 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
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-Related structure data
Related structure data | ![]() 7zqjC ![]() 5gjxS S: Starting model for refinement 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
-Protein , 2 types, 2 molecules AB
#1: Protein | Mass: 31630.094 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: exon 2-4 Source: (gene. exp.) ![]() Organ: liver / Production host: ![]() ![]() |
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#2: Protein | Mass: 14205.976 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: N-terminal His6-tag, TEV-cleavage site Source: (gene. exp.) ![]() Gene: B2M / Production host: ![]() ![]() |
-Protein/peptide , 1 types, 1 molecules F
#3: Protein/peptide | Mass: 1073.261 Da / Num. of mol.: 1 / Source method: obtained synthetically / Details: synthetic peptide / Source: (synth.) ![]() |
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-Non-polymers , 4 types, 170 molecules 






#4: Chemical | ChemComp-MG / |
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#5: Chemical | ChemComp-CL / |
#6: Chemical | ChemComp-MPD / ( |
#7: Water | ChemComp-HOH / |
-Details
Has ligand of interest | N |
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Has protein modification | Y |
-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.06 Å3/Da / Density % sol: 40.29 % |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 7 Details: 100 mM Hepes/MOPS, pH 7.0, 20 mM MgCl2, 40 mM CaCl2, 25 % (v/v) MPD, 25 % (w/v) PEG 1000, 25 % (w/v) PEG 3350 |
-Data collection
Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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Diffraction source | Source: ![]() ![]() ![]() |
Detector | Type: DECTRIS EIGER X 16M / Detector: PIXEL / Date: May 12, 2019 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.9794 Å / Relative weight: 1 |
Reflection | Resolution: 2.15→67.38 Å / Num. obs: 22044 / % possible obs: 99.9 % / Redundancy: 13 % / CC1/2: 0.999 / Net I/σ(I): 12.1 |
Reflection shell | Resolution: 2.15→2.21 Å / Redundancy: 13.4 % / Mean I/σ(I) obs: 1.9 / Num. unique obs: 1759 / CC1/2: 0.848 / % possible all: 99.8 |
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Processing
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Refinement | Method to determine structure: ![]() Starting model: 5GJX Resolution: 2.15→50.58 Å / Cor.coef. Fo:Fc: 0.967 / Cor.coef. Fo:Fc free: 0.948 / SU B: 13.893 / SU ML: 0.174 / Cross valid method: THROUGHOUT / ESU R: 0.262 / ESU R Free: 0.201 / 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: 49.065 Å2
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Refinement step | Cycle: 1 / Resolution: 2.15→50.58 Å
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Refine LS restraints |
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