scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1030849454 |
P356 | DOI | 10.1038/SJ.ONC.1203434 |
P698 | PubMed publication ID | 10713666 |
P5875 | ResearchGate publication ID | 12601506 |
P50 | author | Alan Fersht | Q537479 |
P2093 | author name string | Henckel J | |
Bullock AN | |||
P2860 | cites work | Covalent and noncovalent modifiers of the p53 protein | Q22009048 |
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A model for p53-induced apoptosis | Q24313374 | ||
Structure of the p53 tumor suppressor bound to the ankyrin and SH3 domains of 53BP2 | Q24314736 | ||
Mdm2 promotes the rapid degradation of p53 | Q24322597 | ||
The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway | Q24336089 | ||
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Thermodynamic stability of wild-type and mutant p53 core domain | Q24648879 | ||
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p53, the cellular gatekeeper for growth and division | Q27860990 | ||
Calculation of protein extinction coefficients from amino acid sequence data | Q27861073 | ||
14-3-3Sigma is required to prevent mitotic catastrophe after DNA damage | Q28145962 | ||
p53 mutations in human cancers | Q28302973 | ||
The folding of an enzyme. II. Substructure of barnase and the contribution of different interactions to protein stability | Q28306210 | ||
Over-production of proteins in Escherichia coli: mutant hosts that allow synthesis of some membrane proteins and globular proteins at high levels | Q29547813 | ||
Determination and analysis of urea and guanidine hydrochloride denaturation curves | Q29616644 | ||
Denaturant m values and heat capacity changes: relation to changes in accessible surface areas of protein unfolding | Q29620340 | ||
p53 protein stability in tumour cells is not determined by mutation but is dependent on Mdm2 binding. | Q30428424 | ||
Evolutionary conservation and somatic mutation hotspot maps of p53: correlation with p53 protein structural and functional features. | Q30432624 | ||
The FHA domain is a modular phosphopeptide recognition motif. | Q33285631 | ||
Mechanisms of p53-mediated apoptosis | Q33538150 | ||
Regulation of p53 protein function through alterations in protein-folding pathways | Q33538159 | ||
From computer simulations to human disease: emerging themes in protein folding | Q33630957 | ||
Molecular epidemiology of human cancer risk: gene-environment interactions and p53 mutation spectrum in human lung cancer | Q33643298 | ||
Characterization of structural p53 mutants which show selective defects in apoptosis but not cell cycle arrest | Q33774492 | ||
Engineered disulfide bonds as probes of the folding pathway of barnase: increasing the stability of proteins against the rate of denaturation | Q34363628 | ||
Structure and function of the p53 tumor suppressor gene: clues for rational cancer therapeutic strategies | Q34400583 | ||
Molecular recognition. Conformational analysis of limited proteolytic sites and serine proteinase protein inhibitors | Q34787907 | ||
Hot-spot mutants of p53 core domain evince characteristic local structural changes. | Q35549859 | ||
Identification of a minimal transforming domain of p53: negative dominance through abrogation of sequence-specific DNA binding | Q36706865 | ||
Analysis of p53 mutants for transcriptional activity | Q36743632 | ||
Semirational design of active tumor suppressor p53 DNA binding domain with enhanced stability | Q36753352 | ||
HSP70 binding sites in the tumor suppressor protein p53. | Q36872778 | ||
Correcting temperature-sensitive protein folding defects | Q37365357 | ||
A temperature-sensitive mutant of human p53. | Q37632919 | ||
A proteolytic fragment from the central region of p53 has marked sequence-specific DNA-binding activity when generated from wild-type but not from oncogenic mutant p53 protein | Q38313694 | ||
p53 mutants without a functional tetramerisation domain are not oncogenic | Q38327509 | ||
In vitro analysis of the dominant negative effect of p53 mutants | Q38334521 | ||
Regulation of mutant p53 temperature-sensitive DNA binding. | Q38352373 | ||
Reactivation of mutant p53 through interaction of a C-terminal peptide with the core domain. | Q39445499 | ||
Analysis of the most representative tumour-derived p53 mutants reveals that changes in protein conformation are not correlated with loss of transactivation or inhibition of cell proliferation. | Q40792701 | ||
Defective protein folding as a basis of human disease | Q40956747 | ||
Temperature sensitivity of human wild-type and mutant p53 proteins expressed in vivo | Q41028721 | ||
Structural aspects of the p53 protein in relation to gene evolution: a second look. | Q41034333 | ||
Allosteric regulation of the thermostability and DNA binding activity of human p53 by specific interacting proteins. CRC Cell Transformation Group | Q41227408 | ||
Local versus nonlocal interactions in protein folding and stability--an experimentalist's point of view | Q41394376 | ||
p53-dependent apoptosis in the absence of transcriptional activation of p53-target genes | Q41454039 | ||
Distinct residues of human p53 implicated in binding to DNA, simian virus 40 large T antigen, 53BP1, and 53BP2. | Q42072409 | ||
Specific interaction between the p53 cellular tumour antigen and major heat shock proteins | Q43512047 | ||
New p53-based anti-cancer therapeutic strategies | Q45856234 | ||
Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53. | Q45856831 | ||
Human tumor-derived p53 proteins exhibit binding site selectivity and temperature sensitivity for transactivation in a yeast-based assay | Q47972885 | ||
Induction of apoptosis in HeLa cells by trans-activation-deficient p53 | Q53461564 | ||
Grabbing phosphoproteins | Q58998120 | ||
Flexibility: the key to p53 function? | Q72121789 | ||
p53 status and the efficacy of cancer therapy in vivo | Q72839445 | ||
Folding intermediates of wild-type and mutants of barnase. I. Use of phi-value analysis and m-values to probe the cooperative nature of the folding pre-equilibrium | Q74461800 | ||
Tumor-suppressor p53: implications for tumor development and prognosis | Q77302676 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1245-1256 | |
P577 | publication date | 2000-03-01 | |
P1433 | published in | Oncogene | Q1568657 |
P1476 | title | Quantitative analysis of residual folding and DNA binding in mutant p53 core domain: definition of mutant states for rescue in cancer therapy | |
P478 | volume | 19 |
Q36120749 | A comparison of multiscale methods for the analysis of molecular dynamics simulations |
Q30704432 | A fast method for predicting amino acid mutations that lead to unfolding. |
Q37415505 | A global suppressor motif for p53 cancer mutants |
Q34333807 | A novel p53 phosphorylation site within the MDM2 ubiquitination signal: II. a model in which phosphorylation at SER269 induces a mutant conformation to p53 |
Q24530763 | A peptide that binds and stabilizes p53 core domain: chaperone strategy for rescue of oncogenic mutants |
Q96019130 | A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants |
Q78477022 | A split-ubiquitin-based assay detects the influence of mutations on the conformational stability of the p53 DNA binding domain in vivo |
Q39458140 | A subset of tumor-derived mutant forms of p53 down-regulate p63 and p73 through a direct interaction with the p53 core domain |
Q37236272 | Aggregation tendencies in the p53 family are modulated by backbone hydrogen bonds |
Q30868722 | Allosteric drugs: thinking outside the active-site box. |
Q33865095 | Altered-function p53 missense mutations identified in breast cancers can have subtle effects on transactivation |
Q52558518 | Aminobenzothiazole derivatives stabilize the thermolabile p53 cancer mutant Y220C and show anticancer activity in p53-Y220C cell lines. |
Q37210555 | An in silico algorithm for identifying stabilizing pockets in proteins: test case, the Y220C mutant of the p53 tumor suppressor protein |
Q49481527 | An in silico approach in predicting the possible mechanism involving restoration of wild-type p53 functions by small molecular weight compounds in tumor cells expressing R273H mutant p53. |
Q34570100 | Assessing TP53 status in human tumours to evaluate clinical outcome |
Q35014385 | Awakening guardian angels: drugging the p53 pathway |
Q51564147 | Binding of Rad51 and other peptide sequences to a promiscuous, highly electrostatic binding site in p53. |
Q36009999 | Bioinformatics and variability in drug response: a protein structural perspective |
Q24800091 | CP-31398, a putative p53-stabilizing molecule tested in mammalian cells and in yeast for its effects on p53 transcriptional activity |
Q34036925 | CRINEPT-TROSY NMR reveals p53 core domain bound in an unfolded form to the chaperone Hsp90. |
Q35946185 | Cancer therapeutic approach based on conformational stabilization of mutant p53 protein by small peptides. |
Q57778801 | Change of Conformation of the DNA-binding Domain of p53 Is the Only Key Element for Binding of and Interference with p73 |
Q57838458 | Characterisation of the BRCT Domains of the Breast Cancer Susceptibility Gene Product BRCA1 |
Q43955939 | Characterization of the p53-rescue drug CP-31398 in vitro and in living cells. |
Q37162374 | Chemopreventive effects of the p53-modulating agents CP-31398 and Prima-1 in tobacco carcinogen-induced lung tumorigenesis in A/J mice |
Q83227500 | Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome |
Q24628577 | Computational identification of a transiently open L1/S3 pocket for reactivation of mutant p53 |
Q38787249 | Constitutive Activation of DNA Damage Checkpoint Signaling Contributes to Mutant p53 Accumulation via Modulation of p53 Ubiquitination |
Q27642314 | Crystal structure of a superstable mutant of human p53 core domain. Insights into the mechanism of rescuing oncogenic mutations |
Q21030644 | Determining biophysical protein stability in lysates by a fast proteolysis assay, FASTpp |
Q34443272 | Differential transactivation by the p53 transcription factor is highly dependent on p53 level and promoter target sequence. |
Q39007874 | Distinct Rayleigh scattering from hot spot mutant p53 proteins reveals cancer cells |
Q58615488 | Dynamics and Molecular Mechanisms of p53 Transcriptional Activation |
Q45023386 | Effect of Y220C mutation on p53 and its rescue mechanism: a computer chemistry approach |
Q51186530 | Effects of common cancer mutations on stability and DNA binding of full-length p53 compared with isolated core domains. |
Q51151705 | Effects of oncogenic mutations and DNA response elements on the binding of p53 to p53-binding protein 2 (53BP2). |
Q39809467 | Effects of stability on the biological function of p53. |
Q34081676 | Effects of temperature on the p53-DNA binding interactions and their dynamical behavior: comparing the wild type to the R248Q mutant. |
Q26822552 | Electrochemistry of nonconjugated proteins and glycoproteins. Toward sensors for biomedicine and glycomics |
Q34058079 | Ensemble-based computational approach discriminates functional activity of p53 cancer and rescue mutants |
Q36492803 | Evaluating Drosophila p53 as a model system for studying cancer mutations |
Q40242926 | Exploiting Transient Protein States for the Design of Small-Molecule Stabilizers of Mutant p53. |
Q34965167 | Expression of galectin-7 is induced in breast cancer cells by mutant p53. |
Q35861153 | FUSE Binding Protein 1 Facilitates Persistent Hepatitis C Virus Replication in Hepatoma Cells by Regulating Tumor Suppressor p53. |
Q30682940 | Factors governing loss and rescue of DNA binding upon single and double mutations in the p53 core domain |
Q36187348 | First-order rate-determining aggregation mechanism of p53 and its implications |
Q33325589 | Flexible nets: disorder and induced fit in the associations of p53 and 14-3-3 with their partners |
Q43043487 | Folding and misfolding mechanisms of the p53 DNA binding domain at physiological temperature |
Q41468886 | Folding of a cyclin box: linking multitarget binding to marginal stability, oligomerization, and aggregation of the retinoblastoma tumor suppressor AB pocket domain |
Q89782502 | Follow the Mutations: Toward Class-Specific, Small-Molecule Reactivation of p53 |
Q47616875 | From mutational inactivation to aberrant gain-of-function: Unraveling the structural basis of mutant p53 oncogenic transition |
Q37808312 | From peptides to proteins: lessons from my years at the Centre for Protein Engineering |
Q41832274 | Functional census of mutation sequence spaces: the example of p53 cancer rescue mutants. |
Q32178579 | Fusaric Acid Induces DNA Damage and Post-Translational Modifications of p53 in Human Hepatocellular Carcinoma (HepG2 ) Cells. |
Q34968621 | Fuse binding protein antagonizes the transcription activity of tumor suppressor protein p53. |
Q57670523 | Gain of function of mutant p53 by coaggregation with multiple tumor suppressors |
Q28068551 | Gain of function of mutant p53: R282W on the peak? |
Q27678152 | Halogen-Enriched Fragment Libraries as Leads for Drug Rescue of Mutant p53 |
Q35181268 | Halogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discovery |
Q43690426 | High thermostability and lack of cooperative DNA binding distinguish the p63 core domain from the homologous tumor suppressor p53. |
Q34287510 | Highly adaptable triple-negative breast cancer cells as a functional model for testing anticancer agents |
Q84551753 | Hsp70 molecular chaperones are required to support p53 tumor suppressor activity under stress conditions |
Q28553055 | Hydrogen Bond Dynamic Propensity Studies for Protein Binding and Drug Design |
Q59126521 | Impact of structural prior knowledge in SNV prediction: Towards causal variant finding in rare disease |
Q51026030 | In vitro folding and characterization of the p53 DNA binding domain. |
Q38418659 | Induction of nuclear translocation of mutant cytoplasmic p53 by geranylgeranoic acid in a human hepatoma cell line |
Q37473855 | Inhibition of azoxymethane-induced colorectal cancer by CP-31398, a TP53 modulator, alone or in combination with low doses of celecoxib in male F344 rats |
Q28000133 | Interaction of p53 with the CCT complex promotes protein folding and wild-type p53 activity |
Q27667399 | Interaction of the p53 DNA-Binding Domain with Its N-Terminal Extension Modulates the Stability of the p53 Tetramer |
Q35844807 | Investigating DNA Binding and Conformational Variation in Temperature Sensitive p53 Cancer Mutants Using QM-MM Simulations. |
Q99712014 | Key Players in the Mutant p53 Team: Small Molecules, Gene Editing, Immunotherapy |
Q58322007 | Kinetic Instability of p53 Core Domain Mutants |
Q36187316 | Kinetic mechanism of p53 oncogenic mutant aggregation and its inhibition |
Q35134797 | Mechanism of initiation of aggregation of p53 revealed by Φ-value analysis |
Q42410745 | Molecular dynamics simulations of p53 DNA-binding domain |
Q42088517 | Molecular mechanisms of functional rescue mediated by P53 tumor suppressor mutations |
Q40002181 | Molecular spectrum of TP53 mutations in plasma cell dyscrasias by next generation sequencing: an Italian cohort study and overview of the literature |
Q41677793 | Multisite aggregation of p53 and implications for drug rescue |
Q36689074 | Mutant p53 induces EZH2 expression and promotes epithelial-mesenchymal transition by disrupting p68-Drosha complex assembly and attenuating miR-26a processing |
Q26770576 | Mutant p53: One, No One, and One Hundred Thousand |
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Q74631439 | NMR spectroscopy reveals the solution dimerization interface of p53 core domains bound to their consensus DNA |
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Q46268031 | Nimbolide reduces CD44 positive cell population and induces mitochondrial apoptosis in pancreatic cancer cells |
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Q38723653 | Nuclear inclusion bodies of mutant and wild-type p53 in cancer: a hallmark of p53 inactivation and proteostasis remodelling by p53 aggregation. |
Q92940029 | Oncogenic Gain of Function in Glioblastoma Is Linked to Mutant p53 Amyloid Oligomers |
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Q38948352 | Peptides and peptidomimetics in the p53/MDM2/MDM4 circuitry - a patent review |
Q50014672 | Pharmacoperones as Novel Therapeutics for Diverse Protein Conformational Diseases |
Q35134517 | Propagation of aggregated p53: Cross-reaction and coaggregation vs. seeding |
Q44145204 | QM-MM simulations on p53-DNA complex: a study of hot spot and rescue mutants |
Q50797771 | R248Q mutation--Beyond p53-DNA binding. |
Q35750128 | RNA polymerase III transcription and cancer |
Q74355214 | RNA polymerase III transcription can be derepressed by oncogenes or mutations that compromise p53 function in tumours and Li-Fraumeni syndrome |
Q26800059 | Reactivating mutant p53 using small molecules as zinc metallochaperones: awakening a sleeping giant in cancer |
Q36777373 | Reactivation of mutant p53: molecular mechanisms and therapeutic potential |
Q58322012 | Recognition of DNA by p53 Core Domain and Location of Intermolecular Contacts of Cooperative Binding |
Q37088668 | Rescue of mutants of the tumor suppressor p53 in cancer cells by a designed peptide |
Q30329984 | Rescuing the function of mutant p53. |
Q93095094 | Residual apoptotic activity of a tumorigenic p53 mutant improves cancer therapy responses |
Q73446293 | Resistance to DNA-damaging agents is discordant from experimental metastatic capacity in MEF ras-transformants-expressing gain of function MTp53 |
Q31041084 | Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound. |
Q36710840 | Restoration of wild-type p53 function in human cancer: relevance for tumor therapy. |
Q30951237 | Reversible aggregation plays a crucial role on the folding landscape of p53 core domain |
Q39205536 | Reviving the guardian of the genome: Small molecule activators of p53. |
Q33795918 | SCH529074, a small molecule activator of mutant p53, which binds p53 DNA binding domain (DBD), restores growth-suppressive function to mutant p53 and interrupts HDM2-mediated ubiquitination of wild type p53 |
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Q64231035 | Simulations of mutant p53 DNA binding domains reveal a novel druggable pocket |
Q27677872 | Small molecule induced reactivation of mutant p53 in cancer cells |
Q34619139 | Small molecule restoration of wildtype structure and function of mutant p53 using a novel zinc-metallochaperone based mechanism |
Q50441463 | Spectroscopic studies on the irreversible heat-induced structural transition of Pin1 |
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Q35531853 | Synthetic metallochaperone ZMC1 rescues mutant p53 conformation by transporting zinc into cells as an ionophore |
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