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Yorodumi- PDB-6oi1: Crystal structure of human WDR5 in complex with monomethyl L-arginine -
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Open data
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Basic information
| Entry | Database: PDB / ID: 6oi1 | ||||||
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| Title | Crystal structure of human WDR5 in complex with monomethyl L-arginine | ||||||
Components | WD repeat-containing protein 5 | ||||||
Keywords | GENE REGULATION / Methylation / Epigenetics / Post-translational modification / Chromatin / Methylarginine | ||||||
| Function / homology | Function and homology informationhistone H3Q5ser reader activity / histone H3K4me1 reader activity / Epigenetic regulation of gene expression by MLL3 and MLL4 complexes / MLL3/4 complex / Set1C/COMPASS complex / MLL1/2 complex / ATAC complex / NSL complex / histone H3K4 methyltransferase activity / Cardiogenesis ...histone H3Q5ser reader activity / histone H3K4me1 reader activity / Epigenetic regulation of gene expression by MLL3 and MLL4 complexes / MLL3/4 complex / Set1C/COMPASS complex / MLL1/2 complex / ATAC complex / NSL complex / histone H3K4 methyltransferase activity / Cardiogenesis / Formation of WDR5-containing histone-modifying complexes / histone methyltransferase complex / regulation of cell division / MLL1 complex / regulation of embryonic development / histone acetyltransferase complex / positive regulation of gluconeogenesis / transcription initiation-coupled chromatin remodeling / gluconeogenesis / skeletal system development / RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function / PKMTs methylate histone lysines / RMTs methylate histone arginines / Activation of anterior HOX genes in hindbrain development during early embryogenesis / mitotic spindle / Neddylation / HATs acetylate histones / MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis / histone binding / regulation of cell cycle / regulation of DNA-templated transcription / regulation of transcription by RNA polymerase II / positive regulation of DNA-templated transcription / negative regulation of transcription by RNA polymerase II / nucleoplasm / nucleus Similarity search - Function | ||||||
| Biological species | Homo sapiens (human) | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.68 Å | ||||||
Authors | Lorton, B.M. / Harijan, R.K. / Burgos, E. / Bonanno, J.B. / Almo, S.C. / Shechter, D. | ||||||
Citation | Journal: Biochemistry / Year: 2020Title: A Binary Arginine Methylation Switch on Histone H3 Arginine 2 Regulates Its Interaction with WDR5. Authors: Lorton, B.M. / Harijan, R.K. / Burgos, E.S. / Bonanno, J.B. / Almo, S.C. / Shechter, D. | ||||||
| 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 | 6oi1.cif.gz | 77.5 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb6oi1.ent.gz | 55.2 KB | Display | PDB format |
| PDBx/mmJSON format | 6oi1.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 6oi1_validation.pdf.gz | 457.3 KB | Display | wwPDB validaton report |
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| Full document | 6oi1_full_validation.pdf.gz | 457.3 KB | Display | |
| Data in XML | 6oi1_validation.xml.gz | 14 KB | Display | |
| Data in CIF | 6oi1_validation.cif.gz | 19.7 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/oi/6oi1 ftp://data.pdbj.org/pub/pdb/validation_reports/oi/6oi1 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6ofzC ![]() 6oi0C ![]() 6oi2C ![]() 6oi3C ![]() 2h14S S: Starting model for refinement C: citing same article ( |
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| Similar structure data |
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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 | Mass: 34390.992 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: WDR5, BIG3 / Production host: ![]() | ||||
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| #2: Chemical | ChemComp-SO4 / | ||||
| #3: Chemical | | #4: Chemical | ChemComp-NMM / ( | #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: 2.1 Å3/Da / Density % sol: 40 % |
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| Crystal grow | Temperature: 295 K / Method: vapor diffusion, sitting drop / pH: 5.9 Details: 100mM Bis-Tris pH 5.9, 32% PEG3350, 54.6 mM Ammonium Sulfate, 0.66 mM monomethyl L-arginine |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
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| Diffraction source | Source: SYNCHROTRON / Site: APS / Beamline: 31-ID / Wavelength: 0.97931 Å |
| Detector | Type: RAYONIX MX225HE / Detector: CCD / Date: Oct 24, 2018 / Details: KB mirrors |
| Radiation | Monochromator: diamond (111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.97931 Å / Relative weight: 1 |
| Reflection | Resolution: 1.68→59.06 Å / Num. obs: 33408 / % possible obs: 100 % / Redundancy: 7.2 % / Rpim(I) all: 0.03 / Net I/σ(I): 14.5 |
| Reflection shell | Resolution: 1.68→1.71 Å / Redundancy: 7.3 % / Mean I/σ(I) obs: 2 / Num. unique obs: 1685 / Rpim(I) all: 0.37 / % possible all: 99.9 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 2H14 Resolution: 1.68→59.06 Å / Cor.coef. Fo:Fc: 0.963 / Cor.coef. Fo:Fc free: 0.951 / SU B: 2.694 / SU ML: 0.086 / Cross valid method: THROUGHOUT / ESU R: 0.114 / ESU R Free: 0.114 / 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 23.785 Å2
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| Refinement step | Cycle: 1 / Resolution: 1.68→59.06 Å
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| Refine LS restraints |
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Homo sapiens (human)
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