Distinct binding modes specify the recognition of methylated histones H3K4 and H4K20 by JMJD2A-tudor
about
Enzymatic and structural insights for substrate specificity of a family of jumonji histone lysine demethylasesThe AAA-ATPase VCP/p97 promotes 53BP1 recruitment by removing L3MBTL1 from DNA double-strand breaksDistinct mode of methylated lysine-4 of histone H3 recognition by tandem tudor-like domains of Spindlin1Phf19 links methylated Lys36 of histone H3 to regulation of Polycomb activityMolecular basis for H3K36me3 recognition by the Tudor domain of PHF1RNF8- and RNF168-dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sitesSgf29 binds histone H3K4me2/3 and is required for SAGA complex recruitment and histone H3 acetylation.Methylation-state-specific recognition of histones by the MBT repeat protein L3MBTL2PHD finger recognition of unmodified histone H3R2 links UHRF1 to regulation of euchromatic gene expressionNucleolar protein Spindlin1 recognizes H3K4 methylation and stimulates the expression of rRNA genesPHF20 is an effector protein of p53 double lysine methylation that stabilizes and activates p53Structural and functional coordination of DNA and histone methylationThe role of histone demethylases in cancer therapyKDM4/JMJD2 histone demethylases: epigenetic regulators in cancer cellsProtein lysine acetylation by p300/CBPHistone demethylase KDM4B regulates otic vesicle invagination via epigenetic control of Dlx3 expression.Structural Basis for the Recognition of Methylated Histone H3K36 by the Eaf3 Subunit of Histone Deacetylase Complex Rpd3SStructure of an atypical Tudor domain in theDrosophilaPolycomblike proteinStructural and Evolutionary Basis for the Dual Substrate Selectivity of Human KDM4 Histone Demethylase FamilySolution Structure and Molecular Interactions of Lamin B Receptor Tudor DomainSolution structure of the Pdp1 PWWP domain reveals its unique binding sites for methylated H4K20 and DNAInhibition of osteogenic differentiation of human adipose-derived stromal cells by retinoblastoma binding protein 2 repression of RUNX2-activated transcriptionErasing the methyl mark: histone demethylases at the center of cellular differentiation and diseaseDirect inhibition of Gcn5 protein catalytic activity by polyglutamine-expanded ataxin-7.Modulation of epigenetic targets for anticancer therapy: clinicopathological relevance, structural data and drug discovery perspectivesA complex small RNA repertoire is generated by a plant/fungal-like machinery and effected by a metazoan-like Argonaute in the single-cell human parasite Toxoplasma gondii.A combinatorial H4 tail library for exploring the histone code.A homogeneous method for investigation of methylation-dependent protein-protein interactions in epigeneticsA method for systematic mapping of protein lysine methylation identifies functions for HP1β in DNA damage response.Expanding the landscape of chromatin modification (CM)-related functional domains and genes in human.Coordinated chromatin control: structural and functional linkage of DNA and histone methylation.Preparation of recombinant peptides with site- and degree-specific lysine (13)C-methylation.JMJD2A contributes to breast cancer progression through transcriptional repression of the tumor suppressor ARHIMolecular recognition of H3/H4 histone tails by the tudor domains of JMJD2A: a comparative molecular dynamics simulations studyA new isoform of the histone demethylase JMJD2A/KDM4A is required for skeletal muscle differentiation.Computational methods for de novo protein design and its applications to the human immunodeficiency virus 1, purine nucleoside phosphorylase, ubiquitin specific protease 7, and histone demethylases.Application of Celluspots peptide arrays for the analysis of the binding specificity of epigenetic reading domains to modified histone tails.Utility-aware screening with clique-oriented prioritization.Nuclear role of WASp in the pathogenesis of dysregulated TH1 immunity in human Wiskott-Aldrich syndrome.The PHD finger: a versatile epigenome reader.
P2860
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P2860
Distinct binding modes specify the recognition of methylated histones H3K4 and H4K20 by JMJD2A-tudor
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
name
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@ast
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@en
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@nl
type
label
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@ast
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@en
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@nl
prefLabel
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@ast
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@en
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@nl
P2093
P2860
P356
P1476
Distinct binding modes specify ...... H3K4 and H4K20 by JMJD2A-tudor
@en
P2093
Georges Mer
James R Thompson
Joseph Lee
Maria Victoria Botuyan
P2860
P2888
P304
P356
10.1038/NSMB1326
P407
P577
2008-01-01T00:00:00Z
P5875
P6179
1013066032