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 *

123 related articles for article (PubMed ID: 9372193)

  • 41. Substrate recognition by the ClpA chaperone component of ClpAP protease.
    Hoskins JR; Kim SY; Wickner S
    J Biol Chem; 2000 Nov; 275(45):35361-7. PubMed ID: 10952988
    [TBL] [Abstract][Full Text] [Related]  

  • 42. ClpS is an essential component of the N-end rule pathway in Escherichia coli.
    Erbse A; Schmidt R; Bornemann T; Schneider-Mergener J; Mogk A; Zahn R; Dougan DA; Bukau B
    Nature; 2006 Feb; 439(7077):753-6. PubMed ID: 16467841
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Global role for ClpP-containing proteases in stationary-phase adaptation of Escherichia coli.
    Weichart D; Querfurth N; Dreger M; Hengge-Aronis R
    J Bacteriol; 2003 Jan; 185(1):115-25. PubMed ID: 12486047
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Degradation of L-glutamate dehydrogenase from Escherichia coli: allosteric regulation of enzyme stability.
    Maurizi MR; Rasulova F
    Arch Biochem Biophys; 2002 Jan; 397(2):206-16. PubMed ID: 11795873
    [TBL] [Abstract][Full Text] [Related]  

  • 45. The N-terminal substrate-binding domain of ClpA unfoldase is highly mobile and extends axially from the distal surface of ClpAP protease.
    Ishikawa T; Maurizi MR; Steven AC
    J Struct Biol; 2004; 146(1-2):180-8. PubMed ID: 15037249
    [TBL] [Abstract][Full Text] [Related]  

  • 46. E. coli ClpA catalyzed polypeptide translocation is allosterically controlled by the protease ClpP.
    Miller JM; Lin J; Li T; Lucius AL
    J Mol Biol; 2013 Aug; 425(15):2795-812. PubMed ID: 23639359
    [TBL] [Abstract][Full Text] [Related]  

  • 47. ClpAP proteolysis does not require rotation of the ClpA unfoldase relative to ClpP.
    Kim S; Zuromski KL; Bell TA; Sauer RT; Baker TA
    Elife; 2020 Dec; 9():. PubMed ID: 33258771
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Protease Ti, a new ATP-dependent protease in Escherichia coli, contains protein-activated ATPase and proteolytic functions in distinct subunits.
    Hwang BJ; Woo KM; Goldberg AL; Chung CH
    J Biol Chem; 1988 Jun; 263(18):8727-34. PubMed ID: 2967816
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The asymmetry in the mature amino-terminus of ClpP facilitates a local symmetry match in ClpAP and ClpXP complexes.
    Bewley MC; Graziano V; Griffin K; Flanagan JM
    J Struct Biol; 2006 Feb; 153(2):113-28. PubMed ID: 16406682
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Processive degradation of proteins by the ATP-dependent Clp protease from Escherichia coli. Requirement for the multiple array of active sites in ClpP but not ATP hydrolysis.
    Thompson MW; Singh SK; Maurizi MR
    J Biol Chem; 1994 Jul; 269(27):18209-15. PubMed ID: 8027082
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Cytoplasmic degradation of ssrA-tagged proteins.
    Farrell CM; Grossman AD; Sauer RT
    Mol Microbiol; 2005 Sep; 57(6):1750-61. PubMed ID: 16135238
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The ClpP N-terminus coordinates substrate access with protease active site reactivity.
    Jennings LD; Bohon J; Chance MR; Licht S
    Biochemistry; 2008 Oct; 47(42):11031-40. PubMed ID: 18816064
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Degradation of mutant initiator protein DnaA204 by proteases ClpP, ClpQ and Lon is prevented when DNA is SeqA-free.
    Slominska M; Wahl A; Wegrzyn G; Skarstad K
    Biochem J; 2003 Mar; 370(Pt 3):867-71. PubMed ID: 12479794
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The flexible attachment of the N-domains to the ClpA ring body allows their use on demand.
    Cranz-Mileva S; Imkamp F; Kolygo K; Maglica Z; Kress W; Weber-Ban E
    J Mol Biol; 2008 Apr; 378(2):412-24. PubMed ID: 18358489
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The first cytoplasmic loop of the mannitol permease from Escherichia coli is accessible for sulfhydryl reagents from the periplasmic side of the membrane.
    Vervoort EB; Bultema JB; Schuurman-Wolters GK; Geertsma ER; Broos J; Poolman B
    J Mol Biol; 2005 Feb; 346(3):733-43. PubMed ID: 15713459
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Importance of heptameric ring integrity for activity of Escherichia coli ClpP.
    Thompson MW; Miller J; Maurizi MR; Kempner E
    Eur J Biochem; 1998 Dec; 258(3):923-8. PubMed ID: 9990309
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Six-fold rotational symmetry of ClpQ, the E. coli homolog of the 20S proteasome, and its ATP-dependent activator, ClpY.
    Kessel M; Wu W; Gottesman S; Kocsis E; Steven AC; Maurizi MR
    FEBS Lett; 1996 Dec; 398(2-3):274-8. PubMed ID: 8977122
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Modular and coordinated activity of AAA+ active sites in the double-ring ClpA unfoldase of the ClpAP protease.
    Zuromski KL; Sauer RT; Baker TA
    Proc Natl Acad Sci U S A; 2020 Oct; 117(41):25455-25463. PubMed ID: 33020301
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Site-directed mutations in motif VI of Escherichia coli DNA helicase II result in multiple biochemical defects: evidence for the involvement of motif VI in the coupling of ATPase and DNA binding activities via conformational changes.
    Hall MC; Ozsoy AZ; Matson SW
    J Mol Biol; 1998 Mar; 277(2):257-71. PubMed ID: 9514760
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The structural basis for the activation and peptide recognition of bacterial ClpP.
    Kim DY; Kim KK
    J Mol Biol; 2008 Jun; 379(4):760-71. PubMed ID: 18468623
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.