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 *

602 related articles for article (PubMed ID: 10876246)

  • 41. Fine tuning of a biological machine: DnaK gains improved chaperone activity by altered allosteric communication and substrate binding.
    Schweizer RS; Aponte RA; Zimmermann S; Weber A; Reinstein J
    Chembiochem; 2011 Jul; 12(10):1559-73. PubMed ID: 21656889
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Kinetic characterization of the ATPase cycle of the DnaK molecular chaperone.
    Russell R; Jordan R; McMacken R
    Biochemistry; 1998 Jan; 37(2):596-607. PubMed ID: 9425082
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Analysis of sequence-specific binding of RNA to Hsp70 and its various homologs indicates the involvement of N- and C-terminal interactions.
    Zimmer C; von Gabain A; Henics T
    RNA; 2001 Nov; 7(11):1628-37. PubMed ID: 11720291
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Its substrate specificity characterizes the DnaJ co-chaperone as a scanning factor for the DnaK chaperone.
    Rüdiger S; Schneider-Mergener J; Bukau B
    EMBO J; 2001 Mar; 20(5):1042-50. PubMed ID: 11230128
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Interaction of the Hsp70 molecular chaperone, DnaK, with its cochaperone DnaJ.
    Suh WC; Burkholder WF; Lu CZ; Zhao X; Gottesman ME; Gross CA
    Proc Natl Acad Sci U S A; 1998 Dec; 95(26):15223-8. PubMed ID: 9860950
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Catapult mechanism renders the chaperone action of Hsp70 unidirectional.
    Gisler SM; Pierpaoli EV; Christen P
    J Mol Biol; 1998 Jun; 279(4):833-40. PubMed ID: 9642064
    [TBL] [Abstract][Full Text] [Related]  

  • 47. All three J-domain proteins of the Escherichia coli DnaK chaperone machinery are DNA binding proteins.
    Gur E; Katz C; Ron EZ
    FEBS Lett; 2005 Mar; 579(9):1935-9. PubMed ID: 15792799
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Studies on the mechanism of catalysis of iron-sulfur cluster transfer from IscU[2Fe2S] by HscA/HscB chaperones.
    Bonomi F; Iametti S; Morleo A; Ta D; Vickery LE
    Biochemistry; 2008 Dec; 47(48):12795-801. PubMed ID: 18986169
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A gram-negative characteristic segment in Escherichia coli DnaK is essential for the ATP-dependent cooperative function with the co-chaperones DnaJ and GrpE.
    Sugimoto S; Higashi C; Saruwatari K; Nakayama J; Sonomoto K
    FEBS Lett; 2007 Jun; 581(16):2993-9. PubMed ID: 17544398
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The DnaK chaperones from the archaeon Methanosarcina mazei and the bacterium Escherichia coli have different substrate specificities.
    Zmijewski MA; Skórko-Glonek J; Tanfani F; Banecki B; Kotlarz A; Macario AJ; Lipińska B
    Acta Biochim Pol; 2007; 54(3):509-22. PubMed ID: 17882322
    [TBL] [Abstract][Full Text] [Related]  

  • 51. GrpE accelerates peptide binding and release from the high affinity state of DnaK.
    Mally A; Witt SN
    Nat Struct Biol; 2001 Mar; 8(3):254-7. PubMed ID: 11224572
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Structure and dynamics of the ATP-bound open conformation of Hsp70 chaperones.
    Kityk R; Kopp J; Sinning I; Mayer MP
    Mol Cell; 2012 Dec; 48(6):863-74. PubMed ID: 23123194
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Substrate specificity of the DnaK chaperone determined by screening cellulose-bound peptide libraries.
    Rüdiger S; Germeroth L; Schneider-Mergener J; Bukau B
    EMBO J; 1997 Apr; 16(7):1501-7. PubMed ID: 9130695
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Importance of two ATP-binding sites for oligomerization, ATPase activity and chaperone function of mitochondrial Hsp78 protein.
    Krzewska J; Konopa G; Liberek K
    J Mol Biol; 2001 Dec; 314(4):901-10. PubMed ID: 11734006
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Sequence-specific rates of interaction of target peptides with the molecular chaperones DnaK and DnaJ.
    Pierpaoli EV; Gisler SM; Christen P
    Biochemistry; 1998 Nov; 37(47):16741-8. PubMed ID: 9843444
    [TBL] [Abstract][Full Text] [Related]  

  • 56. High-throughput screen for small molecules that modulate the ATPase activity of the molecular chaperone DnaK.
    Chang L; Bertelsen EB; Wisén S; Larsen EM; Zuiderweg ER; Gestwicki JE
    Anal Biochem; 2008 Jan; 372(2):167-76. PubMed ID: 17904512
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A Trypanosoma cruzi heat shock protein 40 is able to stimulate the adenosine triphosphate hydrolysis activity of heat shock protein 70 and can substitute for a yeast heat shock protein 40.
    Edkins AL; Ludewig MH; Blatch GL
    Int J Biochem Cell Biol; 2004 Aug; 36(8):1585-98. PubMed ID: 15147737
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Kinetic evidence for peptide-induced oligomerization of the molecular chaperone DnaK at heat shock temperatures.
    Farr CD; Witt SN
    Biochemistry; 1997 Sep; 36(35):10793-800. PubMed ID: 9271511
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Functional properties of the molecular chaperone DnaK from Thermus thermophilus.
    Klostermeier D; Seidel R; Reinstein J
    J Mol Biol; 1998 Jun; 279(4):841-53. PubMed ID: 9642065
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The carboxyl-terminal lobe of Hsc70 ATPase domain is sufficient for binding to BAG1.
    Brive L; Takayama S; Briknarová K; Homma S; Ishida SK; Reed JC; Ely KR
    Biochem Biophys Res Commun; 2001 Dec; 289(5):1099-105. PubMed ID: 11741305
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 31.