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Journal Abstract Search

123 related items for PubMed ID: 4694149

  • 1. A numerical method for acquisition and processing of steady-state kinetic data contained in an entire progression curve. Application to the study of -chymotrypsin-catalyzed hydrolysis.
    Bizzozero S, Kaiser AW, Dutler H.
    Eur J Biochem; 1973 Mar 01; 33(2):292-300. PubMed ID: 4694149
    [No Abstract] [Full Text] [Related]

  • 2. Chymotrypsin-catalyzed phenyl ester hydrolysis. Evidence for electrophilic assistance on carbonyl oxygen.
    Williams A.
    Biochemistry; 1970 Aug 18; 9(17):3383-90. PubMed ID: 5522470
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  • 3. 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 18; 71(5):1643-7. PubMed ID: 4525454
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  • 6. 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 01; 58(1):167-76. PubMed ID: 1183433
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  • 10. 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 03; 12(14):2559-66. PubMed ID: 4711463
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  • 12. A comparison of the utilization of methyl and p-nitrophenyl esters in determining the specificity of -chymotrypsin.
    Silver MS, Matta MS.
    Arch Biochem Biophys; 1972 Jul 03; 151(1):62-7. PubMed ID: 5044527
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  • 16. [Kinetics of alpha-chymotrypsin catalyzed hydrolysis in equilibrium. II. Comparison of ester and amide substrates].
    Gurova AG, Ginodman LM, Antonov VK.
    Mol Biol (Mosk); 1977 Jul 03; 11(5):1155-9. PubMed ID: 618342
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