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Open data
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Basic information
Entry | Database: PDB / ID: 2ka6 | ||||||
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Title | NMR structure of the CBP-TAZ2/STAT1-TAD complex | ||||||
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![]() | TRANSCRIPTION REGULATOR / CBP/p300 / TAZ2 / STAT1 / transactivation domain / Bromodomain / Activator / Alternative splicing / Antiviral defense / Cytoplasm / Disease mutation / DNA-binding / Host-virus interaction / Nucleus / Phosphoprotein / Polymorphism / SH2 domain / Transcription / Transcription regulation / Acetylation / Chromosomal rearrangement / Metal-binding / Methylation / Transferase / Ubl conjugation / Zinc / Zinc-finger | ||||||
Function / homology | ![]() metanephric mesenchymal cell differentiation / negative regulation of metanephric nephron tubule epithelial cell differentiation / negative regulation by virus of viral protein levels in host cell / renal tubule development / ISGF3 complex / Activation of the TFAP2 (AP-2) family of transcription factors / Regulation of FOXO transcriptional activity by acetylation / TRAF6 mediated IRF7 activation / Nuclear events mediated by NFE2L2 / response to interferon-beta ...metanephric mesenchymal cell differentiation / negative regulation of metanephric nephron tubule epithelial cell differentiation / negative regulation by virus of viral protein levels in host cell / renal tubule development / ISGF3 complex / Activation of the TFAP2 (AP-2) family of transcription factors / Regulation of FOXO transcriptional activity by acetylation / TRAF6 mediated IRF7 activation / Nuclear events mediated by NFE2L2 / response to interferon-beta / Attenuation phase / LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production / metanephric mesenchymal cell proliferation involved in metanephros development / Regulation of gene expression by Hypoxia-inducible Factor / RUNX1 regulates transcription of genes involved in differentiation of myeloid cells / Formation of the beta-catenin:TCF transactivating complex / NOTCH1 Intracellular Domain Regulates Transcription / RUNX3 regulates NOTCH signaling / cAMP response element binding protein binding / Notch-HLH transcription pathway / Transcriptional and post-translational regulation of MITF-M expression and activity / negative regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis / interleukin-27-mediated signaling pathway / CCR5 chemokine receptor binding / germ-line stem cell population maintenance / negative regulation of viral process / Regulation of lipid metabolism by PPARalpha / Interleukin-9 signaling / Interleukin-21 signaling / interleukin-7-mediated signaling pathway / interleukin-9-mediated signaling pathway / Cytoprotection by HMOX1 / Estrogen-dependent gene expression / CD209 (DC-SIGN) signaling / peptide lactyltransferase (CoA-dependent) activity / outer kinetochore / negative regulation of interferon-beta production / Interleukin-27 signaling / N-terminal peptidyl-lysine acetylation / Interleukin-35 Signalling / Signaling by cytosolic FGFR1 fusion mutants / tumor necrosis factor receptor binding / cell surface receptor signaling pathway via STAT / MRF binding / face morphogenesis / blood circulation / positive regulation of mesenchymal cell proliferation / NOTCH3 Intracellular Domain Regulates Transcription / Interleukin-20 family signaling / negative regulation of transcription by RNA polymerase I / Interleukin-6 signaling / protein-lysine-acetyltransferase activity / type I interferon-mediated signaling pathway / cellular response to hepatocyte growth factor stimulus / histone acetyltransferase binding / histone acetyltransferase activity / acetyltransferase activity / negative regulation of endothelial cell proliferation / : / ubiquitin-like protein ligase binding / Regulation of IFNA/IFNB signaling / positive regulation of interferon-alpha production / TFIIB-class transcription factor binding / histone acetyltransferase complex / response to type II interferon / cell surface receptor signaling pathway via JAK-STAT / type II interferon-mediated signaling pathway / Regulation of IFNG signaling / positive regulation of double-strand break repair via homologous recombination / Growth hormone receptor signaling / Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants / Signaling by PDGFRA extracellular domain mutants / cellular response to interferon-beta / RNA polymerase II core promoter sequence-specific DNA binding / Signaling by CSF3 (G-CSF) / histone H4K16 acetyltransferase activity / response to mechanical stimulus / histone H3K56 acetyltransferase activity / histone H3K23 acetyltransferase activity / histone H2AK5 acetyltransferase activity / histone H2AK9 acetyltransferase activity / histone H2BK5 acetyltransferase activity / histone H2BK12 acetyltransferase activity / histone H3K4 acetyltransferase activity / histone H3K27 acetyltransferase activity / histone H3K36 acetyltransferase activity / histone H3K122 acetyltransferase activity / histone H3K18 acetyltransferase activity / histone H3K9 acetyltransferase activity / histone H3K14 acetyltransferase activity / histone H4K5 acetyltransferase activity / histone H4K8 acetyltransferase activity / histone H4K12 acetyltransferase activity / histone acetyltransferase / response to cAMP / tumor necrosis factor-mediated signaling pathway / negative regulation of canonical NF-kappaB signal transduction / positive regulation of defense response to virus by host / Transferases; Acyltransferases; Transferring groups other than aminoacyl groups / response to nutrient Similarity search - Function | ||||||
Biological species | ![]() ![]() ![]() | ||||||
Method | SOLUTION NMR / molecular dynamics | ||||||
![]() | Wojciak, J.M. / Martinez-Yamout, M.A. / Dyson, H.J. / Wright, P.E. | ||||||
![]() | ![]() Title: Structural basis for recruitment of CBP/p300 coactivators by STAT1 and STAT2 transactivation domains. Authors: Wojciak, J.M. / Martinez-Yamout, M.A. / Dyson, H.J. / Wright, P.E. | ||||||
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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PDBx/mmCIF format | ![]() | 836.5 KB | Display | ![]() |
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PDB format | ![]() | 714.4 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
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-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
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-Related structure data
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Links
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Assembly
Deposited unit | ![]()
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NMR ensembles |
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Components
#1: Protein | Mass: 10527.567 Da / Num. of mol.: 1 / Fragment: UNP residues 1764 to 1855 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() ![]() |
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#2: Protein/peptide | Mass: 5041.582 Da / Num. of mol.: 1 / Fragment: UNP residues 710 to 750 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() |
#3: Chemical |
-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR |
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NMR experiment | Type: 2D 1H-15N ![]() |
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Sample preparation
Details | Contents: 1 mM [U-100% 15N] TAZ2, 90% H2O/10% D2O / Solvent system: 90% H2O/10% D2O |
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Sample | Conc.: 1 mM / Component: TAZ2 / Isotopic labeling: [U-100% 15N] |
Sample conditions | Ionic strength: 0.05 / pH: 6.8 / Pressure: ambient / Temperature: 290 K |
-NMR measurement
NMR spectrometer |
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Processing
NMR software | Name: ![]() Developer: Case, Darden, Cheatham, III, Simmerling, Wang, Duke, Luo, ... and Kollm Classification: refinement |
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Refinement | Method: molecular dynamics / Software ordinal: 1 |
NMR representative | Selection criteria: closest to the average |
NMR ensemble | Conformer selection criteria: structures with the lowest energy Conformers calculated total number: 200 / Conformers submitted total number: 20 |