BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

436 related articles for article (PubMed ID: 19016865)

  • 1. Mycobacterium tuberculosis ClpC1: characterization and role of the N-terminal domain in its function.
    Kar NP; Sikriwal D; Rath P; Choudhary RK; Batra JK
    FEBS J; 2008 Dec; 275(24):6149-58. PubMed ID: 19016865
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Mycobacterium tuberculosis ClpP1P2 Protease Interacts Asymmetrically with Its ATPase Partners ClpX and ClpC1.
    Leodolter J; Warweg J; Weber-Ban E
    PLoS One; 2015; 10(5):e0125345. PubMed ID: 25933022
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The chaperone function of ClpB from Thermus thermophilus depends on allosteric interactions of its two ATP-binding sites.
    Schlee S; Groemping Y; Herde P; Seidel R; Reinstein J
    J Mol Biol; 2001 Mar; 306(4):889-99. PubMed ID: 11243796
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The C-terminus of ClpC1 of Mycobacterium tuberculosis is crucial for its oligomerization and function.
    Bajaj D; Batra JK
    PLoS One; 2012; 7(12):e51261. PubMed ID: 23284674
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A domain in the N-terminal part of Hsp26 is essential for chaperone function and oligomerization.
    Haslbeck M; Ignatiou A; Saibil H; Helmich S; Frenzl E; Stromer T; Buchner J
    J Mol Biol; 2004 Oct; 343(2):445-55. PubMed ID: 15451672
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic and transcriptional organization of the clpC locus in Bifidobacterium breve UCC 2003.
    Ventura M; Fitzgerald GF; van Sinderen D
    Appl Environ Microbiol; 2005 Oct; 71(10):6282-91. PubMed ID: 16204550
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation analysis of the interactions between Mycobacterium tuberculosis caseinolytic protease C1 (ClpC1) and ecumicin.
    Jung IP; Ha NR; Kim AR; Kim SH; Yoon MY
    Int J Biol Macromol; 2017 Aug; 101():348-357. PubMed ID: 28342755
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structure, stability, and chaperone function of alphaA-crystallin: role of N-terminal region.
    Kundu M; Sen PC; Das KP
    Biopolymers; 2007 Jun; 86(3):177-92. PubMed ID: 17345631
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Negative regulation of AAA + ATPase assembly by two component receiver domains: a transcription activation mechanism that is conserved in mesophilic and extremely hyperthermophilic bacteria.
    Doucleff M; Chen B; Maris AE; Wemmer DE; Kondrashkina E; Nixon BT
    J Mol Biol; 2005 Oct; 353(2):242-55. PubMed ID: 16169010
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Crystal structure of proteolytic fragments of the redox-sensitive Hsp33 with constitutive chaperone activity.
    Kim SJ; Jeong DG; Chi SW; Lee JS; Ryu SE
    Nat Struct Biol; 2001 May; 8(5):459-66. PubMed ID: 11323724
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oxygen binding and NO scavenging properties of truncated hemoglobin, HbN, of Mycobacterium smegmatis.
    Lama A; Pawaria S; Dikshit KL
    FEBS Lett; 2006 Jul; 580(17):4031-41. PubMed ID: 16814781
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MecA, an adaptor protein necessary for ClpC chaperone activity.
    Schlothauer T; Mogk A; Dougan DA; Bukau B; Turgay K
    Proc Natl Acad Sci U S A; 2003 Mar; 100(5):2306-11. PubMed ID: 12598648
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of bis-ANS binding sites in Mycobacterium tuberculosis small heat shock protein Hsp16.3: evidences for a two-step substrate-binding mechanism.
    Fu X; Chang Z
    Biochem Biophys Res Commun; 2006 Oct; 349(1):167-71. PubMed ID: 16930542
    [TBL] [Abstract][Full Text] [Related]  

  • 14. M domains couple the ClpB threading motor with the DnaK chaperone activity.
    Haslberger T; Weibezahn J; Zahn R; Lee S; Tsai FT; Bukau B; Mogk A
    Mol Cell; 2007 Jan; 25(2):247-60. PubMed ID: 17244532
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional and structural characterization of Helicobacter pylori ClpX: a molecular chaperone of Hsp100 family.
    Rath P; Singh PK; Batra JK
    Protein Pept Lett; 2012 Dec; 19(12):1263-71. PubMed ID: 22670669
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structural and functional roles for beta-strand 7 in the alpha-crystallin domain of p26, a polydisperse small heat shock protein from Artemia franciscana.
    Sun Y; Bojikova-Fournier S; MacRae TH
    FEBS J; 2006 Mar; 273(5):1020-34. PubMed ID: 16478475
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Conformational properties of bacterial DnaK and yeast mitochondrial Hsp70. Role of the divergent C-terminal alpha-helical subdomain.
    Moro F; Fernández-Sáiz V; Slutsky O; Azem A; Muga A
    FEBS J; 2005 Jun; 272(12):3184-96. PubMed ID: 15955075
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Agrobacterium tumefaciens DnaK: ATPase cycle, oligomeric state and chaperone properties.
    Boshoff A; Stephens LL; Blatch GL
    Int J Biochem Cell Biol; 2008; 40(4):804-12. PubMed ID: 18061511
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of novel sequence motifs within N- and C-terminal extensions of p26, a small heat shock protein from Artemia franciscana.
    Sun Y; MacRae TH
    FEBS J; 2005 Oct; 272(20):5230-43. PubMed ID: 16218954
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biochemical and physiological studies of the small heat shock protein Lo18 from the lactic acid bacterium Oenococcus oeni.
    Delmas F; Pierre F; Coucheney F; Divies C; Guzzo J
    J Mol Microbiol Biotechnol; 2001 Oct; 3(4):601-10. PubMed ID: 11545277
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.