BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1888 related articles for article (PubMed ID: 15497503)

  • 21. S100A1 is a novel molecular chaperone and a member of the Hsp70/Hsp90 multichaperone complex.
    Okada M; Hatakeyama T; Itoh H; Tokuta N; Tokumitsu H; Kobayashi R
    J Biol Chem; 2004 Feb; 279(6):4221-33. PubMed ID: 14638689
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Domain:domain interactions within Hop, the Hsp70/Hsp90 organizing protein, are required for protein stability and structure.
    Carrigan PE; Sikkink LA; Smith DF; Ramirez-Alvarado M
    Protein Sci; 2006 Mar; 15(3):522-32. PubMed ID: 16452615
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Regulation of the Hsp90-binding immunophilin, cyclophilin 40, is mediated by multiple sites for GA-binding protein (GABP).
    Kumar P; Ward BK; Minchin RF; Ratajczak T
    Cell Stress Chaperones; 2001 Jan; 6(1):78-91. PubMed ID: 11525247
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Stimulation of the weak ATPase activity of human hsp90 by a client protein.
    McLaughlin SH; Smith HW; Jackson SE
    J Mol Biol; 2002 Jan; 315(4):787-98. PubMed ID: 11812147
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Importance of the C-terminal domain of Harc for binding to Hsp70 and Hop as well as its response to heat shock.
    Cartledge K; Elsegood C; Roiniotis J; Hamilton JA; Scholz GM
    Biochemistry; 2007 Dec; 46(51):15144-52. PubMed ID: 18052042
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hop as an adaptor in the heat shock protein 70 (Hsp70) and hsp90 chaperone machinery.
    Chen S; Smith DF
    J Biol Chem; 1998 Dec; 273(52):35194-200. PubMed ID: 9857057
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of FKBP51/FKBP52 chimeras and mutants for Hsp90 binding and association with progesterone receptor complexes.
    Barent RL; Nair SC; Carr DC; Ruan Y; Rimerman RA; Fulton J; Zhang Y; Smith DF
    Mol Endocrinol; 1998 Mar; 12(3):342-54. PubMed ID: 9514152
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Efficient Hsp90-independent in vitro activation by Hsc70 and Hsp40 of duck hepatitis B virus reverse transcriptase, an assumed Hsp90 client protein.
    Beck J; Nassal M
    J Biol Chem; 2003 Sep; 278(38):36128-38. PubMed ID: 12851401
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The chaperone function of cyclophilin 40 maps to a cleft between the prolyl isomerase and tetratricopeptide repeat domains.
    Mok D; Allan RK; Carrello A; Wangoo K; Walkinshaw MD; Ratajczak T
    FEBS Lett; 2006 May; 580(11):2761-8. PubMed ID: 16650407
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Small glutamine-rich protein/viral protein U-binding protein is a novel cochaperone that affects heat shock protein 70 activity.
    Angeletti PC; Walker D; Panganiban AT
    Cell Stress Chaperones; 2002 Jul; 7(3):258-68. PubMed ID: 12482202
    [TBL] [Abstract][Full Text] [Related]  

  • 31. In silico identification of carboxylate clamp type tetratricopeptide repeat proteins in Arabidopsis and rice as putative co-chaperones of Hsp90/Hsp70.
    Prasad BD; Goel S; Krishna P
    PLoS One; 2010 Sep; 5(9):e12761. PubMed ID: 20856808
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Quantitative assessment of complex formation of nuclear-receptor accessory proteins.
    Graumann K; Jungbauer A
    Biochem J; 2000 Feb; 345 Pt 3(Pt 3):627-36. PubMed ID: 10642522
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Maturation of steroid receptors: an example of functional cooperation among molecular chaperones and their associated proteins.
    Kimmins S; MacRae TH
    Cell Stress Chaperones; 2000 Apr; 5(2):76-86. PubMed ID: 11147968
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chaperone-interacting TPR proteins in Caenorhabditis elegans.
    Haslbeck V; Eckl JM; Kaiser CJ; Papsdorf K; Hessling M; Richter K
    J Mol Biol; 2013 Aug; 425(16):2922-39. PubMed ID: 23727266
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Different combinations of the heat-shock cognate protein 70 (hsc70) C-terminal functional groups are utilized to interact with distinct tetratricopeptide repeat-containing proteins.
    Wu SJ; Liu FH; Hu SM; Wang C
    Biochem J; 2001 Oct; 359(Pt 2):419-26. PubMed ID: 11583590
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Specific binding of tetratricopeptide repeat proteins to the C-terminal 12-kDa domain of hsp90.
    Young JC; Obermann WM; Hartl FU
    J Biol Chem; 1998 Jul; 273(29):18007-10. PubMed ID: 9660753
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multiple domains of the co-chaperone Hop are important for Hsp70 binding.
    Carrigan PE; Nelson GM; Roberts PJ; Stoffer J; Riggs DL; Smith DF
    J Biol Chem; 2004 Apr; 279(16):16185-93. PubMed ID: 14960564
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Differential effects of the hsp70-binding protein BAG-1 on glucocorticoid receptor folding by the hsp90-based chaperone machinery.
    Kanelakis KC; Morishima Y; Dittmar KD; Galigniana MD; Takayama S; Reed JC; Pratt WB
    J Biol Chem; 1999 Nov; 274(48):34134-40. PubMed ID: 10567384
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Structural studies on the co-chaperone Hop and its complexes with Hsp90.
    Onuoha SC; Coulstock ET; Grossmann JG; Jackson SE
    J Mol Biol; 2008 Jun; 379(4):732-44. PubMed ID: 18485364
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Functional and physical interaction between yeast Hsp90 and Hsp70.
    Kravats AN; Hoskins JR; Reidy M; Johnson JL; Doyle SM; Genest O; Masison DC; Wickner S
    Proc Natl Acad Sci U S A; 2018 Mar; 115(10):E2210-E2219. PubMed ID: 29463764
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 95.