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 *

134 related articles for article (PubMed ID: 2878928)

  • 1. Biosynthetic thiolase from Zoogloea ramigera. II. Inactivation with haloacetyl CoA analogs.
    Davis JT; Chen HH; Moore R; Nishitani Y; Masamune S; Sinskey AJ; Walsh CT
    J Biol Chem; 1987 Jan; 262(1):90-6. PubMed ID: 2878928
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Biosynthetic thiolase from zoogloea ramigera. I. Preliminary characterization and analysis of proton transfer reaction.
    Davis JT; Moore RN; Imperiali B; Pratt AJ; Kobayashi K; Masamune S; Sinskey AJ; Walsh CT; Fukui T; Tomita K
    J Biol Chem; 1987 Jan; 262(1):82-9. PubMed ID: 2878927
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biosynthetic thiolase from Zoogloea ramigera. Evidence for a mechanism involving Cys-378 as the active site base.
    Palmer MA; Differding E; Gamboni R; Williams SF; Peoples OP; Walsh CT; Sinskey AJ; Masamune S
    J Biol Chem; 1991 May; 266(13):8369-75. PubMed ID: 1673680
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Crystallographic analysis of the reaction pathway of Zoogloea ramigera biosynthetic thiolase.
    Modis Y; Wierenga RK
    J Mol Biol; 2000 Apr; 297(5):1171-82. PubMed ID: 10764581
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The catalytic cycle of biosynthetic thiolase: a conformational journey of an acetyl group through four binding modes and two oxyanion holes.
    Kursula P; Ojala J; Lambeir AM; Wierenga RK
    Biochemistry; 2002 Dec; 41(52):15543-56. PubMed ID: 12501183
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mechanistic studies on beta-ketoacyl thiolase from Zoogloea ramigera: identification of the active-site nucleophile as Cys89, its mutation to Ser89, and kinetic and thermodynamic characterization of wild-type and mutant enzymes.
    Thompson S; Mayerl F; Peoples OP; Masamune S; Sinskey AJ; Walsh CT
    Biochemistry; 1989 Jul; 28(14):5735-42. PubMed ID: 2775734
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Examination of the role of thiolimidate formation in the cleavage of acetoacetyl-CoA catalyzed by thiolase I from porcine heart.
    Izbicka E; Gilbert HF
    Arch Biochem Biophys; 1989 Aug; 272(2):476-80. PubMed ID: 2568819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The thiolase reaction mechanism: the importance of Asn316 and His348 for stabilizing the enolate intermediate of the Claisen condensation.
    Meriläinen G; Poikela V; Kursula P; Wierenga RK
    Biochemistry; 2009 Nov; 48(46):11011-25. PubMed ID: 19842716
    [TBL] [Abstract][Full Text] [Related]  

  • 9. On the active site of liver acetyl-CoA. Arylamine N-acetyltransferase from rapid acetylator rabbits (III/J).
    Andres HH; Klem AJ; Schopfer LM; Harrison JK; Weber WW
    J Biol Chem; 1988 Jun; 263(16):7521-7. PubMed ID: 2897358
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The reaction of acetyldithio-CoA, a readily enolized analog of acetyl-CoA with thiolase from Zoogloea ramigera.
    Anderson VE; Bahnson BJ; Wlassics ID; Walsh CT
    J Biol Chem; 1990 Apr; 265(11):6255-61. PubMed ID: 2180945
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biosynthetic thiolase from Zoogloea ramigera. Mutagenesis of the putative active-site base Cys-378 to Ser-378 changes the partitioning of the acetyl S-enzyme intermediate.
    Williams SF; Palmer MA; Peoples OP; Walsh CT; Sinskey AJ; Masamune S
    J Biol Chem; 1992 Aug; 267(23):16041-3. PubMed ID: 1353760
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The sulfur atoms of the substrate CoA and the catalytic cysteine are required for a productive mode of substrate binding in bacterial biosynthetic thiolase, a thioester-dependent enzyme.
    Meriläinen G; Schmitz W; Wierenga RK; Kursula P
    FEBS J; 2008 Dec; 275(24):6136-48. PubMed ID: 19016856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A biosynthetic thiolase in complex with a reaction intermediate: the crystal structure provides new insights into the catalytic mechanism.
    Modis Y; Wierenga RK
    Structure; 1999 Oct; 7(10):1279-90. PubMed ID: 10545327
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mechanism of action of beta-oxoacyl-CoA thiolase from rat liver cytosol. Direct evidence for the order of addition of the two acetyl-CoA molecules during the formation of acetoacetyl-CoA.
    Jordan PM; Gibbs PN
    Biochem J; 1983 Jul; 213(1):153-8. PubMed ID: 6137209
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of subsidiary catalytic groups at the active site of beta-ketoacyl-CoA thiolase by covalent modification of the protein.
    Salam WH; Bloxham DP
    Biochim Biophys Acta; 1986 Oct; 873(3):321-30. PubMed ID: 2875737
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biosynthetic thiolase from Zoogloea ramigera. III. Isolation and characterization of the structural gene.
    Peoples OP; Masamune S; Walsh CT; Sinskey AJ
    J Biol Chem; 1987 Jan; 262(1):97-102. PubMed ID: 2878929
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Selective inhibition of cholesterol synthesis by cell-free preparations of rat liver by using inhibitors of cytoplasmic acetoacetyl-coenzyme A thiolase.
    Bloxham DP
    Biochem J; 1975 Jun; 147(3):531-9. PubMed ID: 241330
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis of chloromethyl ketone derivatives of fatty acids. Their use as specific inhibitors of acetoacetyl-coenzyme A thiolase, cholesterol biosynthesis and fatty acid synthesis.
    Bloxham DP; Chalkley RA; Coghlin SJ; Salam W
    Biochem J; 1978 Dec; 175(3):999-1011. PubMed ID: 33667
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Streptomyces collinus thiolase with novel acetyl-CoA:acyl carrier protein transacylase activity.
    Lobo S; Florova G; Reynolds KA
    Biochemistry; 2001 Oct; 40(39):11955-64. PubMed ID: 11570897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. S-(4-Bromo-2,3-dioxobutyl)CoA: an affinity label for certain enzymes than bind acetyl-CoA.
    Owens MS; Barden RE
    Arch Biochem Biophys; 1978 Apr; 187(2):299-306. PubMed ID: 27142
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.