Structural insights into the interaction and activation of histone deacetylase 3 by nuclear receptor corepressors. - Wikidata - wikimedia - TriplyDB

Structural insights into the interaction and activation of histone deacetylase 3 by nuclear receptor corepressors.

Structural insights into the interaction and activation of histone deacetylase 3 by nuclear receptor corepressors.

http://www.wikidata.org/entity/Q33771012

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Activation of p53 transcriptional activity by SMRT: a histone deacetylase 3-independent function of a transcriptional corepressor Corepressors: custom tailoring and alterations while you wait.Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors Histone deacetylase 3 interacts with and deacetylates myocyte enhancer factor 2 GEI-8, a homologue of vertebrate nuclear receptor corepressor NCoR/SMRT, regulates gonad development and neuronal functions in Caenorhabditis elegans Structural basis for the assembly of the SMRT/NCoR core transcriptional repression machinery Structure of HDAC3 bound to co-repressor and inositol tetraphosphate Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells IkappaB kinase alpha-mediated derepression of SMRT potentiates acetylation of RelA/p65 by p300.NCoR1 mediates papillomavirus E8;E2C transcriptional repression NCoR repression of LXRs restricts macrophage biosynthesis of insulin-sensitizing omega 3 fatty acids.Hdac3 is essential for the maintenance of chromatin structure and genome stability.Regulation of SMRT corepressor dimerization and composition by MAP kinase phosphorylation.Nuclear receptor corepressor complexes in cancer: mechanism, function and regulation Identification of putative interactions between swine and human influenza A virus nucleoprotein and human host proteins Methylation levels of SLC23A2 and NCOR2 genes correlate with spinal muscular atrophy severity.Short-chain fatty acids induce gamma-globin gene expression by displacement of a HDAC3-NCoR repressor complex.Ligands of Therapeutic Utility for the Liver X Receptors.Structural Characterization of the SMRT Corepressor Interacting with Histone Deacetylase 7.Autoregulatory loop of nuclear corepressor 1 expression controls invasion, tumor growth, and metastasis Drosophila Ebi mediates Snail-dependent transcriptional repression through HDAC3-induced histone deacetylation.Nuclear receptor co-repressors are required for the histone-deacetylase activity of HDAC3 in vivo.HDAC4 promotes growth of colon cancer cells via repression of p21.Effects of the SANT domain of tension-induced/inhibited proteins (TIPs), novel partners of the histone acetyltransferase p300, on p300 activity and TIP-6-induced adipogenesis.Photoreactive "nanorulers" detect a novel conformation of full length HDAC3-SMRT complex in solution The dual role of LSD1 and HDAC3 in STAT5-dependent transcription is determined by protein interactions, binding affinities, motifs and genomic positions.Modulation of cell cycle regulators by HDACs.HDAC3 and the molecular brake pad hypothesis Nuclear hormone receptor co-repressors: structure and function.Nuclear phosphoinositide regulation of chromatin.Distinct HDACs regulate the transcriptional response of human cyclin-dependent kinase inhibitor genes to Trichostatin A and 1alpha,25-dihydroxyvitamin D3.Small-molecule hormones: molecular mechanisms of action Structural insight into the separate roles of inositol tetraphosphate and deacetylase-activating domain in activation of histone deacetylase 3 A conserved acidic patch in the Myb domain is required for activation of an endogenous target gene and for chromatin binding.Inactivating mutation in histone deacetylase 3 stabilizes its active conformation.Nuclear hormone receptor architecture - form and dynamics: The 2009 FASEB Summer Conference on Dynamic Structure of the Nuclear Hormone Receptors.Relationship Between Histone Deacetylase 3 (HDAC3) and Breast Cancer.Histone deacetylase 3 promotes liver regeneration and liver cancer cells proliferation through signal transducer and activator of transcription 3 signaling pathway.Implications of STAT3 and STAT5 signaling on gene regulation and chromatin remodeling in hematopoietic cancer

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Structural insights into the interaction and activation of histone deacetylase 3 by nuclear receptor corepressors.

http://www.wikidata.org/entity/Q33771012

description

2005 nî lūn-bûn

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2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2005 թվականի ապրիլին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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Structural insights into the i ...... nuclear receptor corepressors.

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Structural insights into the i ...... nuclear receptor corepressors.

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Structural insights into the i ...... nuclear receptor corepressors

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P2093

Anna Codina

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David Neuhaus

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James D Love

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Mitchell A Lazar

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Yun Li

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P2860

Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation

A core SMRT corepressor complex containing HDAC3 and TBL1, a WD40-repeat protein linked to deafness

Enzymatic activity associated with class II HDACs is dependent on a multiprotein complex containing HDAC3 and SMRT/N-CoR

The N-CoR-HDAC3 nuclear receptor corepressor complex inhibits the JNK pathway through the integral subunit GPS2

Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-gamma

Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor

Oligomerization of ETO is obligatory for corepressor interaction

Solution structure of a DNA-binding unit of Myb: a helix-turn-helix-related motif with conserved tryptophans forming a hydrophobic core

Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3

Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression

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