BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 28232883)

  • 1. Using chemical shifts to generate structural ensembles for intrinsically disordered proteins with converged distributions of secondary structure.
    Ytreberg FM; Borcherds W; Wu H; Daughdrill GW
    Intrinsically Disord Proteins; 2015; 3(1):e984565. PubMed ID: 28232883
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural divergence is more extensive than sequence divergence for a family of intrinsically disordered proteins.
    Borcherds W; Kashtanov S; Wu H; Daughdrill GW
    Proteins; 2013 Oct; 81(10):1686-98. PubMed ID: 23606624
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impact of the K24N mutation on the transactivation domain of p53 and its binding to murine double-minute clone 2.
    Zhan YA; Wu H; Powell AT; Daughdrill GW; Ytreberg FM
    Proteins; 2013 Oct; 81(10):1738-47. PubMed ID: 23609977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. p53 Phosphomimetics Preserve Transient Secondary Structure but Reduce Binding to Mdm2 and MdmX.
    Levy R; Gregory E; Borcherds W; Daughdrill G
    Biomolecules; 2019 Mar; 9(3):. PubMed ID: 30832340
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular Dynamics Simulations Combined with Nuclear Magnetic Resonance and/or Small-Angle X-ray Scattering Data for Characterizing Intrinsically Disordered Protein Conformational Ensembles.
    Chan-Yao-Chong M; Durand D; Ha-Duong T
    J Chem Inf Model; 2019 May; 59(5):1743-1758. PubMed ID: 30840442
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Residual Structures and Transient Long-Range Interactions of p53 Transactivation Domain: Assessment of Explicit Solvent Protein Force Fields.
    Liu X; Chen J
    J Chem Theory Comput; 2019 Aug; 15(8):4708-4720. PubMed ID: 31241933
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phosphorylation Regulates the Bound Structure of an Intrinsically Disordered Protein: The p53-TAZ2 Case.
    Ithuralde RE; Turjanski AG
    PLoS One; 2016; 11(1):e0144284. PubMed ID: 26742101
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Modulation of the disordered conformational ensembles of the p53 transactivation domain by cancer-associated mutations.
    Ganguly D; Chen J
    PLoS Comput Biol; 2015 Apr; 11(4):e1004247. PubMed ID: 25897952
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Using chemical shifts to assess transient secondary structure and generate ensemble structures of intrinsically disordered proteins.
    Kashtanov S; Borcherds W; Wu H; Daughdrill GW; Ytreberg FM
    Methods Mol Biol; 2012; 895():139-52. PubMed ID: 22760318
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Conformational propensities of intrinsically disordered proteins from NMR chemical shifts.
    Kragelj J; Ozenne V; Blackledge M; Jensen MR
    Chemphyschem; 2013 Sep; 14(13):3034-45. PubMed ID: 23794453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Application of the maximum entropy principle to determine ensembles of intrinsically disordered proteins from residual dipolar couplings.
    Sanchez-Martinez M; Crehuet R
    Phys Chem Chem Phys; 2014 Dec; 16(47):26030-9. PubMed ID: 25358803
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A J-modulated protonless NMR experiment characterizes the conformational ensemble of the intrinsically disordered protein WIP.
    Rozentur-Shkop E; Goobes G; Chill JH
    J Biomol NMR; 2016 Dec; 66(4):243-257. PubMed ID: 27844185
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structure and disorder in an unfolded state under nondenaturing conditions from ensemble models consistent with a large number of experimental restraints.
    Marsh JA; Forman-Kay JD
    J Mol Biol; 2009 Aug; 391(2):359-74. PubMed ID: 19501099
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Understanding the structural ensembles of a highly extended disordered protein.
    Daughdrill GW; Kashtanov S; Stancik A; Hill SE; Helms G; Muschol M; Receveur-Bréchot V; Ytreberg FM
    Mol Biosyst; 2012 Jan; 8(1):308-19. PubMed ID: 21979461
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recognition of the disordered p53 transactivation domain by the transcriptional adapter zinc finger domains of CREB-binding protein.
    Krois AS; Ferreon JC; Martinez-Yamout MA; Dyson HJ; Wright PE
    Proc Natl Acad Sci U S A; 2016 Mar; 113(13):E1853-62. PubMed ID: 26976603
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Generating Intrinsically Disordered Protein Conformational Ensembles from a Database of Ramachandran Space Pair Residue Probabilities Using a Markov Chain.
    Cukier RI
    J Phys Chem B; 2018 Oct; 122(39):9087-9101. PubMed ID: 30204435
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ensemble Calculation for Intrinsically Disordered Proteins Using NMR Parameters.
    Kragelj J; Blackledge M; Jensen MR
    Adv Exp Med Biol; 2015; 870():123-47. PubMed ID: 26387101
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural Ensembles of Intrinsically Disordered Proteins Depend Strongly on Force Field: A Comparison to Experiment.
    Rauscher S; Gapsys V; Gajda MJ; Zweckstetter M; de Groot BL; Grubmüller H
    J Chem Theory Comput; 2015 Nov; 11(11):5513-24. PubMed ID: 26574339
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NMR chemical shift and relaxation measurements provide evidence for the coupled folding and binding of the p53 transactivation domain.
    Vise PD; Baral B; Latos AJ; Daughdrill GW
    Nucleic Acids Res; 2005; 33(7):2061-77. PubMed ID: 15824059
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Modulation of p53 Transactivation Domain Conformations by Ligand Binding and Cancer-Associated Mutations.
    Liu X; Chen J
    Pac Symp Biocomput; 2020; 25():195-206. PubMed ID: 31797597
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.