p53 contains large unstructured regions in its native state.
about
Identification, analysis, and prediction of protein ubiquitination sitesQuaternary structures of tumor suppressor p53 and a specific p53 DNA complexNMR chemical shift and relaxation measurements provide evidence for the coupled folding and binding of the p53 transactivation domainStructure and apoptotic function of p73Involvement of p53 in the repair of DNA double strand breaks: multifaceted Roles of p53 in homologous recombination repair (HRR) and non-homologous end joining (NHEJ)Acetylation of lysine 382 and phosphorylation of serine 392 in p53 modulate the interaction between p53 and MDC1 in vitrop53 dynamics upon response element recognition explored by molecular simulations.Structure of the MDM2/MDMX RING domain heterodimer reveals dimerization is required for their ubiquitylation in transSystematic Mutational Analysis of Peptide Inhibition of the p53–MDM2/MDMX InteractionsFunctional anthology of intrinsic disorder. 1. Biological processes and functions of proteins with long disordered regions.Reversible aggregation plays a crucial role on the folding landscape of p53 core domain.The proline repeat domain of p53 binds directly to the transcriptional coactivator p300 and allosterically controls DNA-dependent acetylation of p53.Intrinsically disordered proteins display no preference for chaperone binding in vivo.Development of an accurate classification system of proteins into structured and unstructured regions that uncovers novel structural domains: its application to human transcription factors.p53 Amino-terminus region (1-125) stabilizes and restores heat denatured p53 wild phenotype.Differences in the transactivation domains of p53 family members: a computational study.Transcriptional repressor domain of MBD1 is intrinsically disordered and interacts with its binding partners in a selective mannerPathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseasesBinary classification of protein molecules into intrinsically disordered and ordered segments.Impact of the K24N mutation on the transactivation domain of p53 and its binding to murine double-minute clone 2Genomic repertoires of DNA-binding transcription factors across the tree of life.Electron microscopy studies on the quaternary structure of p53 reveal different binding modes for p53 tetramers in complex with DNARecognition of RNA by the p53 tumor suppressor protein in the yeast three-hybrid system.Acetylation of mouse p53 at lysine 317 negatively regulates p53 apoptotic activities after DNA damageEthylenediamine functionalized-single-walled nanotube (f-SWNT)-assisted in vitro delivery of the oncogene suppressor p53 gene to breast cancer MCF-7 cells.Structural basis for understanding oncogenic p53 mutations and designing rescue drugs.Direct observations of conformational distributions of intrinsically disordered p53 peptides using UV Raman and explicit solvent simulationsPositive cooperative mechanistic binding of proteins at low concentrations: a comparison of poly (sodium N-undecanoyl sulfate) and sodium dodecyl sulfate.Surf the post-translational modification network of p53 regulationRational design of p53, an intrinsically unstructured protein, for the fabrication of novel molecular sensorsMolecular dynamic simulation insights into the normal state and restoration of p53 function.Diffusion NMR spectroscopy: folding and aggregation of domains in p53.Restoration of DNA-binding and growth-suppressive activity of mutant forms of p53 via a PCAF-mediated acetylation pathwayReactivation of mutant p53: molecular mechanisms and therapeutic potential.Understanding the structural ensembles of a highly extended disordered protein.S-nitrosation of glutathione transferase p1-1 is controlled by the conformation of a dynamic active site helix.Versatile functions of p53 protein in multicellular organismsA careful disorderliness in the proteome: sites for interaction and targets for future therapies.Knitting and untying the protein network: modulation of protein ensembles as a therapeutic strategy.Bipartite tetracysteine display requires site flexibility for ReAsH coordination
P2860
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P2860
p53 contains large unstructured regions in its native state.
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
p53 contains large unstructured regions in its native state.
@ast
p53 contains large unstructured regions in its native state.
@en
p53 contains large unstructured regions in its native state.
@nl
type
label
p53 contains large unstructured regions in its native state.
@ast
p53 contains large unstructured regions in its native state.
@en
p53 contains large unstructured regions in its native state.
@nl
prefLabel
p53 contains large unstructured regions in its native state.
@ast
p53 contains large unstructured regions in its native state.
@en
p53 contains large unstructured regions in its native state.
@nl
P2093
P1476
p53 contains large unstructured regions in its native state.
@en
P2093
Christian Klein
Johannes Buchner
Lin Müller
Silke Hansen
Stefan Bell
P304
P356
10.1016/S0022-2836(02)00848-3
P407
P577
2002-10-01T00:00:00Z