These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 19564956)

  • 1. Relative stabilities of conserved and non-conserved structures in the OB-fold superfamily.
    Guardino KM; Sheftic SR; Slattery RE; Alexandrescu AT
    Int J Mol Sci; 2009 May; 10(5):2412-2430. PubMed ID: 19564956
    [TBL] [Abstract][Full Text] [Related]  

  • 2. NMR hydrogen exchange of the OB-fold protein LysN as a function of denaturant: the most conserved elements of structure are the most stable to unfolding.
    Alexandrescu AT; Jaravine VA; Dames SA; Lamour FP
    J Mol Biol; 1999 Jun; 289(4):1041-54. PubMed ID: 10369781
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nucleic acid recognition by OB-fold proteins.
    Theobald DL; Mitton-Fry RM; Wuttke DS
    Annu Rev Biophys Biomol Struct; 2003; 32():115-33. PubMed ID: 12598368
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NMR structure of a stable "OB-fold" sub-domain isolated from staphylococcal nuclease.
    Alexandrescu AT; Gittis AG; Abeygunawardana C; Shortle D
    J Mol Biol; 1995 Jul; 250(2):134-43. PubMed ID: 7608966
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partially folded states of staphylococcal nuclease highlight the conserved structural hierarchy of OB-fold proteins.
    Watson E; Matousek WM; Irimies EL; Alexandrescu AT
    Biochemistry; 2007 Aug; 46(33):9484-94. PubMed ID: 17661445
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Solution structure of the active domain of tissue inhibitor of metalloproteinases-2. A new member of the OB fold protein family.
    Williamson RA; Martorell G; Carr MD; Murphy G; Docherty AJ; Freedman RB; Feeney J
    Biochemistry; 1994 Oct; 33(39):11745-59. PubMed ID: 7918391
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Conservation and Divergence of the I-Domain Inserted into the Ubiquitous HK97 Coat Protein Fold in P22-Like Bacteriophages.
    Tripler TN; Kaplan AR; Alexandrescu AT; Teschke CM
    J Virol; 2019 May; 93(9):. PubMed ID: 30787158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. OB(oligonucleotide/oligosaccharide binding)-fold: common structural and functional solution for non-homologous sequences.
    Murzin AG
    EMBO J; 1993 Mar; 12(3):861-7. PubMed ID: 8458342
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Folding of beta/alpha-unit scrambled forms of S. cerevisiae triosephosphate isomerase: Evidence for autonomy of substructure formation and plasticity of hydrophobic and hydrogen bonding interactions in core of (beta/alpha)8-barrel.
    Shukla A; Guptasarma P
    Proteins; 2004 May; 55(3):548-57. PubMed ID: 15103619
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A conserved tryptophan (W91) at the barrel-lid junction modulates the packing and stability of Kunitz (STI) family of inhibitors.
    Majumder S; Khamrui S; Banerjee R; Bhowmik P; Sen U
    Biochim Biophys Acta; 2015 Jan; 1854(1):55-64. PubMed ID: 25448016
    [TBL] [Abstract][Full Text] [Related]  

  • 11. OB-fold: growing bigger with functional consistency.
    Agrawal V; Kishan KV
    Curr Protein Pept Sci; 2003 Jun; 4(3):195-206. PubMed ID: 12769718
    [TBL] [Abstract][Full Text] [Related]  

  • 12. OB-fold domains: a snapshot of the evolution of sequence, structure and function.
    Arcus V
    Curr Opin Struct Biol; 2002 Dec; 12(6):794-801. PubMed ID: 12504685
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Conserved buried water molecules enable the β-trefoil architecture.
    Blaber M
    Protein Sci; 2020 Aug; 29(8):1794-1802. PubMed ID: 32542709
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structural features can be unconserved in proteins with similar folds. An analysis of side-chain to side-chain contacts secondary structure and accessibility.
    Russell RB; Barton GJ
    J Mol Biol; 1994 Dec; 244(3):332-50. PubMed ID: 7966343
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional evolution of two subtly different (similar) folds.
    Agrawal V; Kishan RK
    BMC Struct Biol; 2001; 1():5. PubMed ID: 11782293
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mechanism of formation of the C-terminal beta-hairpin of the B3 domain of the immunoglobulin binding protein G from Streptococcus. I. Importance of hydrophobic interactions in stabilization of beta-hairpin structure.
    Skwierawska A; Makowska J; Ołdziej S; Liwo A; Scheraga HA
    Proteins; 2009 Jun; 75(4):931-53. PubMed ID: 19089955
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Equilibrium Ensembles for Insulin Folding from Bias-Exchange Metadynamics.
    Singh R; Bansal R; Rathore AS; Goel G
    Biophys J; 2017 Apr; 112(8):1571-1585. PubMed ID: 28445749
    [TBL] [Abstract][Full Text] [Related]  

  • 18. BOF: a novel family of bacterial OB-fold proteins.
    Ginalski K; Kinch L; Rychlewski L; Grishin NV
    FEBS Lett; 2004 Jun; 567(2-3):297-301. PubMed ID: 15178340
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three topologically equivalent core residues affect the transition state ensemble in a protein folding reaction.
    Heidary DK; Jennings PA
    J Mol Biol; 2002 Feb; 316(3):789-98. PubMed ID: 11866531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Conservation of inter-residue interactions and prediction of folding rates of domain repeats.
    Mary RD; Saravanan MK; Selvaraj S
    J Biomol Struct Dyn; 2015; 33(3):534-51. PubMed ID: 24702623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.