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 *

169 related articles for article (PubMed ID: 11104767)

  • 1. Pseudo-T-even bacteriophage RB49 encodes CocO, a cochaperonin for GroEL, which can substitute for Escherichia coli's GroES and bacteriophage T4's Gp31.
    Ang D; Richardson A; Mayer MP; Keppel F; Krisch H; Georgopoulos C
    J Biol Chem; 2001 Mar; 276(12):8720-6. PubMed ID: 11104767
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bacteriophage-encoded cochaperonins can substitute for Escherichia coli's essential GroES protein.
    Keppel F; Rychner M; Georgopoulos C
    EMBO Rep; 2002 Sep; 3(9):893-8. PubMed ID: 12189177
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic analysis of the bacteriophage T4-encoded cochaperonin Gp31.
    Richardson A; Georgopoulos C
    Genetics; 1999 Aug; 152(4):1449-57. PubMed ID: 10430575
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of bacteriophage-encoded cochaperonins.
    Ang D; Keppel F; Klein G; Richardson A; Georgopoulos C
    Annu Rev Genet; 2000; 34():439-456. PubMed ID: 11092834
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The T4-encoded cochaperonin, gp31, has unique properties that explain its requirement for the folding of the T4 major capsid protein.
    Bakkes PJ; Faber BW; van Heerikhuizen H; van der Vies SM
    Proc Natl Acad Sci U S A; 2005 Jun; 102(23):8144-9. PubMed ID: 15919824
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Compensatory changes in GroEL/Gp31 affinity as a mechanism for allele-specific genetic interaction.
    Richardson A; van der Vies SM; Keppel F; Taher A; Landry SJ; Georgopoulos C
    J Biol Chem; 1999 Jan; 274(1):52-8. PubMed ID: 9867810
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bacteriophage T4 encodes a co-chaperonin that can substitute for Escherichia coli GroES in protein folding.
    van der Vies SM; Gatenby AA; Georgopoulos C
    Nature; 1994 Apr; 368(6472):654-6. PubMed ID: 7908418
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An expanded protein folding cage in the GroEL-gp31 complex.
    Clare DK; Bakkes PJ; van Heerikhuizen H; van der Vies SM; Saibil HR
    J Mol Biol; 2006 May; 358(3):905-11. PubMed ID: 16549073
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Substrate mutations that bypass a specific Cpn10 chaperonin requirement for protein folding.
    Andreadis JD; Black LW
    J Biol Chem; 1998 Dec; 273(51):34075-86. PubMed ID: 9852065
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dissociation kinetics of the GroEL-gp31 chaperonin complex studied with Förster resonance energy transfer.
    Calmat S; Hendriks J; van Heerikhuizen H; Schmidt CF; van der Vies SM; Peterman EJ
    Biochemistry; 2009 Dec; 48(49):11692-8. PubMed ID: 19899806
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interplay of structure and disorder in cochaperonin mobile loops.
    Landry SJ; Taher A; Georgopoulos C; van der Vies SM
    Proc Natl Acad Sci U S A; 1996 Oct; 93(21):11622-7. PubMed ID: 8876186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An ORFan no more: the bacteriophage T4 39.2 gene product, NwgI, modulates GroEL chaperone function.
    Ang D; Georgopoulos C
    Genetics; 2012 Mar; 190(3):989-1000. PubMed ID: 22234860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. From minichaperone to GroEL 2: importance of avidity of the multisite ring structure.
    Chatellier J; Hill F; Fersht AR
    J Mol Biol; 2000 Dec; 304(5):883-96. PubMed ID: 11124034
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effective ATPase activity and moderate chaperonin-cochaperonin interaction are important for the functional single-ring chaperonin system.
    Illingworth M; Salisbury J; Li W; Lin D; Chen L
    Biochem Biophys Res Commun; 2015 Oct; 466(1):15-20. PubMed ID: 26271593
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distinct Stabilities of the Structurally Homologous Heptameric Co-Chaperonins GroES and gp31.
    Dyachenko A; Tamara S; Heck AJR
    J Am Soc Mass Spectrom; 2019 Jan; 30(1):7-15. PubMed ID: 29736602
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of important amino acid residues that modulate binding of Escherichia coli GroEL to its various cochaperones.
    Klein G; Georgopoulos C
    Genetics; 2001 Jun; 158(2):507-17. PubMed ID: 11404317
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The importance of a mobile loop in regulating chaperonin/ co-chaperonin interaction: humans versus Escherichia coli.
    Richardson A; Schwager F; Landry SJ; Georgopoulos C
    J Biol Chem; 2001 Feb; 276(7):4981-7. PubMed ID: 11050098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chaperonin complex with a newly folded protein encapsulated in the folding chamber.
    Clare DK; Bakkes PJ; van Heerikhuizen H; van der Vies SM; Saibil HR
    Nature; 2009 Jan; 457(7225):107-10. PubMed ID: 19122642
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural adaptations in the specialized bacteriophage T4 co-chaperonin Gp31 expand the size of the Anfinsen cage.
    Hunt JF; van der Vies SM; Henry L; Deisenhofer J
    Cell; 1997 Jul; 90(2):361-71. PubMed ID: 9244309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chaperonin function depends on structure and disorder in co-chaperonin mobile loops.
    Landry SJ; Steede NK; Garaudy AM; Maskos K; Viitanen PV
    Pac Symp Biocomput; 1999; ():520-31. PubMed ID: 10380224
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.