+Open data
-Basic information
Entry | Database: PDB / ID: 5xjd | ||||||
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Title | TEAD in complex with fragment | ||||||
Components | Transcriptional enhancer factor TEF-3 | ||||||
Keywords | TRANSCRIPTION / transcription factor | ||||||
Function / homology | Function and homology information RUNX3 regulates YAP1-mediated transcription / YAP1- and WWTR1 (TAZ)-stimulated gene expression / trophectodermal cell fate commitment / hippo signaling / blastocyst formation / cell fate specification / positive regulation of stem cell population maintenance / cell fate commitment / embryonic organ development / embryo implantation ...RUNX3 regulates YAP1-mediated transcription / YAP1- and WWTR1 (TAZ)-stimulated gene expression / trophectodermal cell fate commitment / hippo signaling / blastocyst formation / cell fate specification / positive regulation of stem cell population maintenance / cell fate commitment / embryonic organ development / embryo implantation / protein-DNA complex / DNA-binding transcription activator activity, RNA polymerase II-specific / in utero embryonic development / transcription regulator complex / sequence-specific DNA binding / DNA-binding transcription factor activity, RNA polymerase II-specific / DNA-binding transcription factor activity / RNA polymerase II cis-regulatory region sequence-specific DNA binding / DNA-templated transcription / regulation of transcription by RNA polymerase II / positive regulation of DNA-templated transcription / positive regulation of transcription by RNA polymerase II / DNA binding / nucleoplasm / cytoplasm Similarity search - Function | ||||||
Biological species | Mus musculus (house mouse) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.22 Å | ||||||
Authors | Kaan, H.Y.K. / Sim, A.Y.L. / Tan, S.K.J. / Verma, C. / Song, H. | ||||||
Funding support | Singapore, 1items
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Citation | Journal: PLoS ONE / Year: 2017 Title: Targeting YAP/TAZ-TEAD protein-protein interactions using fragment-based and computational modeling approaches. Authors: Kaan, H.Y.K. / Sim, A.Y.L. / Tan, S.K.J. / Verma, C. / Song, H. #1: Journal: Sci Rep / Year: 2017 Title: Crystal structure of TAZ-TEAD complex reveals a distinct interaction mode from that of YAP-TEAD complex. Authors: Kaan, H.Y.K. / Chan, S.W. / Tan, S.K.J. / Guo, F. / Lim, C.J. / Hong, W. / Song, H. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 5xjd.cif.gz | 188.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb5xjd.ent.gz | 150.6 KB | Display | PDB format |
PDBx/mmJSON format | 5xjd.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 5xjd_validation.pdf.gz | 464.9 KB | Display | wwPDB validaton report |
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Full document | 5xjd_full_validation.pdf.gz | 468.4 KB | Display | |
Data in XML | 5xjd_validation.xml.gz | 17.8 KB | Display | |
Data in CIF | 5xjd_validation.cif.gz | 24.9 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/xj/5xjd ftp://data.pdbj.org/pub/pdb/validation_reports/xj/5xjd | HTTPS FTP |
-Related structure data
Related structure data | 3l15S S: Starting model for refinement |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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Noncrystallographic symmetry (NCS) | NCS domain:
NCS domain segments: Component-ID: _ / Ens-ID: 1 / Beg auth comp-ID: ARG / Beg label comp-ID: ARG / End auth comp-ID: VAL / End label comp-ID: VAL / Refine code: _ / Auth seq-ID: 210 - 425 / Label seq-ID: 3 - 218
NCS ensembles :
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-Components
#1: Protein | Mass: 25775.168 Da / Num. of mol.: 2 / Fragment: UNP residues 210-427 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Mus musculus (house mouse) / Gene: Tead4, Tcf13r1, Tef3, Tefr1 / Production host: Escherichia coli (E. coli) / References: UniProt: Q62296 #2: Chemical | ChemComp-87L / ( | #3: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 3.4 Å3/Da / Density % sol: 63.8 % |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 8.4 Details: 2.6M sodium formate, 0.1M Tris pH 8.4, 5 % glycerol, 2mM magnesium chloride |
-Data collection
Diffraction | Mean temperature: 193 K |
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Diffraction source | Source: SYNCHROTRON / Site: NSRRC / Beamline: BL13B1 / Wavelength: 0.987 Å |
Detector | Type: ADSC QUANTUM 315r / Detector: CCD / Date: May 2, 2014 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.987 Å / Relative weight: 1 |
Reflection | Resolution: 2.2→30 Å / Num. obs: 36473 / % possible obs: 99.9 % / Redundancy: 11 % / Net I/σ(I): 8.3 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: 3L15 Resolution: 2.22→30 Å / Cor.coef. Fo:Fc: 0.952 / Cor.coef. Fo:Fc free: 0.941 / SU B: 8.585 / SU ML: 0.107 / Cross valid method: THROUGHOUT / ESU R: 0.19 / ESU R Free: 0.163 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
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Solvent computation | Ion probe radii: 0.7 Å / Shrinkage radii: 0.7 Å / VDW probe radii: 1 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 48.659 Å2
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Refinement step | Cycle: 1 / Resolution: 2.22→30 Å
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Refine LS restraints |
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