112 related articles for article (PubMed ID: 16522085)
1. Design of a hyperstable protein by rational consideration of unfolded state interactions.
Anil B; Craig-Schapiro R; Raleigh DP
J Am Chem Soc; 2006 Mar; 128(10):3144-5. PubMed ID: 16522085
[TBL] [Abstract][Full Text] [Related]
2. The unfolded state of NTL9 is compact in the absence of denaturant.
Anil B; Li Y; Cho JH; Raleigh DP
Biochemistry; 2006 Aug; 45(33):10110-6. PubMed ID: 16906769
[TBL] [Abstract][Full Text] [Related]
3. Exploiting the right side of the Ramachandran plot: substitution of glycines by D-alanine can significantly increase protein stability.
Anil B; Song B; Tang Y; Raleigh DP
J Am Chem Soc; 2004 Oct; 126(41):13194-5. PubMed ID: 15479052
[TBL] [Abstract][Full Text] [Related]
4. 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; 287(2):395-407. PubMed ID: 10080901
[TBL] [Abstract][Full Text] [Related]
5. Dramatic stabilization of an SH3 domain by a single substitution: roles of the folded and unfolded states.
Mok YK; Elisseeva EL; Davidson AR; Forman-Kay JD
J Mol Biol; 2001 Mar; 307(3):913-28. PubMed ID: 11273710
[TBL] [Abstract][Full Text] [Related]
6. 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; 368(1):256-62. PubMed ID: 17337003
[TBL] [Abstract][Full Text] [Related]
7. Thermodynamics and kinetics of non-native interactions in protein folding: a single point mutant significantly stabilizes the N-terminal domain of L9 by modulating non-native interactions in the denatured state.
Cho JH; Sato S; Raleigh DP
J Mol Biol; 2004 May; 338(4):827-37. PubMed ID: 15099748
[TBL] [Abstract][Full Text] [Related]
8. Effects of varying the local propensity to form secondary structure on the stability and folding kinetics of a rapid folding mixed alpha/beta protein: characterization of a truncation mutant of the N-terminal domain of the ribosomal protein L9.
Luisi DL; Kuhlman B; Sideras K; Evans PA; Raleigh DP
J Mol Biol; 1999 May; 289(1):167-74. PubMed ID: 10339414
[TBL] [Abstract][Full Text] [Related]
9. Use of the novel fluorescent amino acid p-cyanophenylalanine offers a direct probe of hydrophobic core formation during the folding of the N-terminal domain of the ribosomal protein L9 and provides evidence for two-state folding.
Aprilakis KN; Taskent H; Raleigh DP
Biochemistry; 2007 Oct; 46(43):12308-13. PubMed ID: 17924662
[TBL] [Abstract][Full Text] [Related]
10. 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; 46(4):1013-21. PubMed ID: 17240985
[TBL] [Abstract][Full Text] [Related]
11. 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; 38(15):4896-903. PubMed ID: 10200179
[TBL] [Abstract][Full Text] [Related]
12. Nonnative electrostatic interactions can modulate protein folding: molecular dynamics with a grain of salt.
Azia A; Levy Y
J Mol Biol; 2009 Oct; 393(2):527-42. PubMed ID: 19683007
[TBL] [Abstract][Full Text] [Related]
13. Rational design, structural and thermodynamic characterization of a hyperstable variant of the villin headpiece helical subdomain.
Bi Y; Cho JH; Kim EY; Shan B; Schindelin H; Raleigh DP
Biochemistry; 2007 Jun; 46(25):7497-505. PubMed ID: 17536785
[TBL] [Abstract][Full Text] [Related]
14. Alpha-helix stabilization by alanine relative to glycine: roles of polar and apolar solvent exposures and of backbone entropy.
López-Llano J; Campos LA; Sancho J
Proteins; 2006 Aug; 64(3):769-78. PubMed ID: 16755589
[TBL] [Abstract][Full Text] [Related]
15. Kinetic isotope effects reveal the presence of significant secondary structure in the transition state for the folding of the N-terminal domain of L9.
Sato S; Raleigh DP
J Mol Biol; 2007 Jul; 370(2):349-55. PubMed ID: 17512540
[TBL] [Abstract][Full Text] [Related]
16. Surface salt bridges, double-mutant cycles, and protein stability: an experimental and computational analysis of the interaction of the Asp 23 side chain with the N-terminus of the N-terminal domain of the ribosomal protein l9.
Luisi DL; Snow CD; Lin JJ; Hendsch ZS; Tidor B; Raleigh DP
Biochemistry; 2003 Jun; 42(23):7050-60. PubMed ID: 12795600
[TBL] [Abstract][Full Text] [Related]
17. Long-range interactions within a nonnative protein.
Klein-Seetharaman J; Oikawa M; Grimshaw SB; Wirmer J; Duchardt E; Ueda T; Imoto T; Smith LJ; Dobson CM; Schwalbe H
Science; 2002 Mar; 295(5560):1719-22. PubMed ID: 11872841
[TBL] [Abstract][Full Text] [Related]
18. The partially folded homodimeric intermediate of Escherichia coli aspartate aminotransferase contains a "molten interface" structure.
Deu E; Dhoot J; Kirsch JF
Biochemistry; 2009 Jan; 48(2):433-41. PubMed ID: 19099423
[TBL] [Abstract][Full Text] [Related]
19. 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; 349(4):839-46. PubMed ID: 15890362
[TBL] [Abstract][Full Text] [Related]
20. Molecular dynamics as a tool to detect protein foldability. A mutant of domain B1 of protein G with non-native secondary structure propensities.
Cregut D; Serrano L
Protein Sci; 1999 Feb; 8(2):271-82. PubMed ID: 10048320
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]