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464 related items for PubMed ID: 15890362

  • 1. Direct characterization of the folded, unfolded and urea-denatured states of the C-terminal domain of the ribosomal protein L9.
    Li Y, Picart F, Raleigh DP.
    J Mol Biol; 2005 Jun 17; 349(4):839-46. PubMed ID: 15890362
    [Abstract] [Full Text] [Related]

  • 2. The cold denatured state is compact but expands at low temperatures: hydrodynamic properties of the cold denatured state of the C-terminal domain of L9.
    Li Y, Shan B, Raleigh DP.
    J Mol Biol; 2007 Apr 20; 368(1):256-62. PubMed ID: 17337003
    [Abstract] [Full Text] [Related]

  • 3. pH dependent thermodynamic and amide exchange studies of the C-terminal domain of the ribosomal protein L9: implications for unfolded state structure.
    Li Y, Horng JC, Raleigh DP.
    Biochemistry; 2006 Jul 18; 45(28):8499-506. PubMed ID: 16834323
    [Abstract] [Full Text] [Related]

  • 4. The unfolded state of NTL9 is compact in the absence of denaturant.
    Anil B, Li Y, Cho JH, Raleigh DP.
    Biochemistry; 2006 Aug 22; 45(33):10110-6. PubMed ID: 16906769
    [Abstract] [Full Text] [Related]

  • 5. Structure and stability of the N-terminal domain of the ribosomal protein L9: evidence for rapid two-state folding.
    Kuhlman B, Boice JA, Fairman R, Raleigh DP.
    Biochemistry; 1998 Jan 27; 37(4):1025-32. PubMed ID: 9454593
    [Abstract] [Full Text] [Related]

  • 6. Analysis of the pH-dependent folding and stability of histidine point mutants allows characterization of the denatured state and transition state for protein folding.
    Horng JC, Cho JH, Raleigh DP.
    J Mol Biol; 2005 Jan 07; 345(1):163-73. PubMed ID: 15567419
    [Abstract] [Full Text] [Related]

  • 7. pH-dependent stability and folding kinetics of a protein with an unusual alpha-beta topology: the C-terminal domain of the ribosomal protein L9.
    Sato S, Raleigh DP.
    J Mol Biol; 2002 Apr 26; 318(2):571-82. PubMed ID: 12051860
    [Abstract] [Full Text] [Related]

  • 8. Conformational analysis of a set of peptides corresponding to the entire primary sequence of the N-terminal domain of the ribosomal protein L9: evidence for stable native-like secondary structure in the unfolded state.
    Luisi DL, Wu WJ, Raleigh DP.
    J Mol Biol; 1999 Mar 26; 287(2):395-407. PubMed ID: 10080901
    [Abstract] [Full Text] [Related]

  • 9. Conformational plasticity of cryptolepain: accumulation of partially unfolded states in denaturants induced equilibrium unfolding.
    Pande M, Dubey VK, Sahu V, Jagannadham MV.
    J Biotechnol; 2007 Sep 30; 131(4):404-17. PubMed ID: 17825936
    [Abstract] [Full Text] [Related]

  • 10. Transient intermediary states with high and low folding probabilities in the apparent two-state folding equilibrium of ACBP at low pH.
    Thomsen JK, Kragelund BB, Teilum K, Knudsen J, Poulsen FM.
    J Mol Biol; 2002 May 03; 318(3):805-14. PubMed ID: 12054824
    [Abstract] [Full Text] [Related]

  • 11. Mutational analysis of the folding transition state of the C-terminal domain of ribosomal protein L9: a protein with an unusual beta-sheet topology.
    Li Y, Gupta R, Cho JH, Raleigh DP.
    Biochemistry; 2007 Jan 30; 46(4):1013-21. PubMed ID: 17240985
    [Abstract] [Full Text] [Related]

  • 12. The denatured state ensemble contains significant local and long-range structure under native conditions: analysis of the N-terminal domain of ribosomal protein L9.
    Meng W, Luan B, Lyle N, Pappu RV, Raleigh DP.
    Biochemistry; 2013 Apr 16; 52(15):2662-71. PubMed ID: 23480024
    [Abstract] [Full Text] [Related]

  • 13. pH and temperature-induced molten globule-like denatured states of equinatoxin II: a study by UV-melting, DSC, far- and near-UV CD spectroscopy, and ANS fluorescence.
    Poklar N, Lah J, Salobir M, Macek P, Vesnaver G.
    Biochemistry; 1997 Nov 25; 36(47):14345-52. PubMed ID: 9398152
    [Abstract] [Full Text] [Related]

  • 14. Folding and domain-domain interactions of the chaperone PapD measured by 19F NMR.
    Bann JG, Frieden C.
    Biochemistry; 2004 Nov 02; 43(43):13775-86. PubMed ID: 15504040
    [Abstract] [Full Text] [Related]

  • 15. Denatured state ensembles with the same radii of gyration can form significantly different long-range contacts.
    Luan B, Lyle N, Pappu RV, Raleigh DP.
    Biochemistry; 2014 Jan 14; 53(1):39-47. PubMed ID: 24280003
    [Abstract] [Full Text] [Related]

  • 16. Structural characterization of unfolded states of apomyoglobin using residual dipolar couplings.
    Mohana-Borges R, Goto NK, Kroon GJ, Dyson HJ, Wright PE.
    J Mol Biol; 2004 Jul 23; 340(5):1131-42. PubMed ID: 15236972
    [Abstract] [Full Text] [Related]

  • 17. pKa values and the pH dependent stability of the N-terminal domain of L9 as probes of electrostatic interactions in the denatured state. Differentiation between local and nonlocal interactions.
    Kuhlman B, Luisi DL, Young P, Raleigh DP.
    Biochemistry; 1999 Apr 13; 38(15):4896-903. PubMed ID: 10200179
    [Abstract] [Full Text] [Related]

  • 18. pH-dependent interactions and the stability and folding kinetics of the N-terminal domain of L9. Electrostatic interactions are only weakly formed in the transition state for folding.
    Luisi DL, Raleigh DP.
    J Mol Biol; 2000 Jun 16; 299(4):1091-100. PubMed ID: 10843860
    [Abstract] [Full Text] [Related]

  • 19. On the relationship between protein stability and folding kinetics: a comparative study of the N-terminal domains of RNase HI, E. coli and Bacillus stearothermophilus L9.
    Sato S, Xiang S, Raleigh DP.
    J Mol Biol; 2001 Sep 21; 312(3):569-77. PubMed ID: 11563917
    [Abstract] [Full Text] [Related]

  • 20. Molecular basis of cooperativity in protein folding. V. Thermodynamic and structural conditions for the stabilization of compact denatured states.
    Xie D, Freire E.
    Proteins; 1994 Aug 21; 19(4):291-301. PubMed ID: 7984625
    [Abstract] [Full Text] [Related]

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