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 *

130 related articles for article (PubMed ID: 4027216)

  • 1. Influence of hydrophobic and steric effects in the acyl group on acylation of alpha-chymotrypsin by N-acylimidazoles.
    Kogan RL; Fife TH
    Biochemistry; 1985 May; 24(11):2610-4. PubMed ID: 4027216
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Electronic effects in the acylation of alpha-chymotrypsin by substituted N-benzoylimidazoles.
    Kogan RL; Fife TH
    Biochemistry; 1984 Jun; 23(13):2983-9. PubMed ID: 6466626
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Binding rates, O--S substitution effects, and the pH dependence of chymotrypsin reactions.
    Hirohara H; Philipp M; Bender ML
    Biochemistry; 1977 Apr; 16(8):1573-80. PubMed ID: 15586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kinetic study on the acylation step of alpha-chymotrypsin-catalyzed hydrolysis of acylimidazole. A model reaction of specific peptide substrate activated by binding to the enzyme.
    Ikeda K; Kunugi S
    J Biochem; 1980 Oct; 88(4):977-86. PubMed ID: 7451425
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mechanisms of acylation of chymotrypsin by phenyl esters of benzoic acid and acetic acid.
    Hubbard CD; Shoupe TS
    J Biol Chem; 1977 Mar; 252(5):1633-8. PubMed ID: 14158
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Catalytic activity of dimeric alpha-chymotrypsin. Acylation kinetics at low pH's.
    Ikeda K; Kunugi S; Hirohara H
    J Biochem; 1980 Mar; 87(3):871-80. PubMed ID: 7390966
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Specificity of -chymotrypsin. Separation of polar, steric, and specific effects in the -chymotrypsin-catalyzed hydrolysis of acyl-substituted p-nitrophenyl esters.
    Dupaix A; Béchet JJ; Roucous C
    Biochemistry; 1973 Jul; 12(14):2559-66. PubMed ID: 4711463
    [No Abstract]   [Full Text] [Related]  

  • 8. Acylation of chymotrypsin by active esters of nonspecific substrates. Evidence for a transient acylimidazole intermediate.
    Hubbard CD; Kirsch JF
    Biochemistry; 1972 Jun; 11(13):2483-93. PubMed ID: 5040654
    [No Abstract]   [Full Text] [Related]  

  • 9. Microenvironmental effects on enzyme catalysis. A kinetic study of hydrophobic derivatives of chymotrypsin.
    Remy MH; Bourdillon C; Thomas D
    Biochim Biophys Acta; 1985 May; 829(1):69-75. PubMed ID: 3995046
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Kinetic investigation of the alpha-chymotrypsin-catalyzed hydrolysis of peptide-ester substrates. The relationship between the structure of the peptide moiety and reactivity.
    Bizzozero SA; Baumann WK; Dutler H
    Eur J Biochem; 1975 Oct; 58(1):167-76. PubMed ID: 1183433
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Separation of polar, steric and specific effects in the alpha-chymotrypsin-catalyzed hydrolysis of acyl-substituted p-nitrophenyl esters.
    Dupaix A; Béchet JJ; Roucous C
    Biochem Biophys Res Commun; 1970 Oct; 41(2):464-70. PubMed ID: 5518177
    [No Abstract]   [Full Text] [Related]  

  • 12. Chemical synthesis of acyl thioesters of acyl carrier protein with native structure.
    Cronan JE; Klages AL
    Proc Natl Acad Sci U S A; 1981 Sep; 78(9):5440-4. PubMed ID: 7029535
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Calorimetric determination of linkage effects involving an acyl-enzyme intermediate.
    Bolen DW; Slightom JL
    Biophys Chem; 1990 Aug; 37(1-3):303-12. PubMed ID: 2285792
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Investigation of diffusion-limited rates of chymotrypsin reactions by viscosity variation.
    Brouwer AC; Kirsch JF
    Biochemistry; 1982 Mar; 21(6):1302-7. PubMed ID: 7074086
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Steady state kinetic evidence for an acyl-enzyme intermediate in reactions catalyzed by bovine spleen cathepsin B.
    Bajkowski AS; Frankfater A
    J Biol Chem; 1983 Feb; 258(3):1645-9. PubMed ID: 6822527
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carboxamidomethyl esters as reactive substrates for alpha-chymotrypsin. Orientational effects of hydrogen-bonding interactions.
    Cohen SG; Torem B; Vaidya V; Ehret A
    J Biol Chem; 1976 Aug; 251(15):4722-8. PubMed ID: 947906
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acylation of alpha-chymotrypsin by oxygen and sulfur esters of specific substrates: kinetic evidence for a tetrahedral intermediate.
    Hiroara H; Bender ML; Stark RS
    Proc Natl Acad Sci U S A; 1974 May; 71(5):1643-7. PubMed ID: 4525454
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparison of the kinetic specificity of subtilisin and thiolsubtilisin toward n-alkyl p-nitrophenyl esters.
    Philipp M; Tsai IH; Bender ML
    Biochemistry; 1979 Aug; 18(17):3769-73. PubMed ID: 38838
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alternate substrate inhibitors of an alpha-chymotrypsin: enantioselective interaction of aryl-substituted enol lactones.
    Baek DJ; Reed PE; Daniels SB; Katzenellenbogen JA
    Biochemistry; 1990 May; 29(18):4305-11. PubMed ID: 2350538
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Acylation of subtilisin Carlsberg by phenyl esters.
    Matta MS; Greene CM; Stein RL; Henderson PA
    J Biol Chem; 1976 Feb; 251(4):1006-8. PubMed ID: 2596
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.