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Journal Abstract Search

238 related items for PubMed ID: 6343835

  • 1. Kinetics of subtilisin and thiolsubtilisin.
    Philipp M, Bender ML.
    Mol Cell Biochem; 1983; 51(1):5-32. PubMed ID: 6343835
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  • 2. Comparison of the kinetic specificity of subtilisin and thiolsubtilisin toward n-alkyl p-nitrophenyl esters.
    Philipp M, Tsai IH, Bender ML.
    Biochemistry; 1979 Aug 21; 18(17):3769-73. PubMed ID: 38838
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  • 6. Evidence that the lack of high catalytic activity of thiolsubtilisin towards specific substrates may be due to an inappropriately located proton-distribution system. Demonstration of highly nucleophilic character of the thiol group of thiolsubtilisin in the catalytically relevant ionization state of the active centre by use of a two-protonic-state reactivity probe.
    Brocklehurst K, Malthouse JP.
    Biochem J; 1981 Mar 01; 193(3):819-23. PubMed ID: 6272719
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  • 7. Engineering substrate preference in subtilisin: structural and kinetic analysis of a specificity mutant.
    Ruan B, London V, Fisher KE, Gallagher DT, Bryan PN.
    Biochemistry; 2008 Jun 24; 47(25):6628-36. PubMed ID: 18507395
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  • 8. Peptic peptide of thiolsubtilisin. Analytical evidence for the chemical transformation of the essential serine-221 to cysteine-221.
    László P, Mihály S.
    Biochim Biophys Acta; 1981 Feb 27; 667(2):351-4. PubMed ID: 6783118
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  • 9. Probing the mechanism and improving the rate of substrate-assisted catalysis in subtilisin BPN'.
    Carter P, Abrahmsén L, Wells JA.
    Biochemistry; 1991 Jun 25; 30(25):6142-8. PubMed ID: 2059622
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  • 10. Mechanism-controlled stereospecificity. Acylation of subtilisin with enantiomeric alkyl and nitrophenyl ester substrates.
    Polgár L, Fejes J.
    Eur J Biochem; 1979 Dec 17; 102(2):531-6. PubMed ID: 43249
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  • 12. Probing the specificity of the S1 binding site of subtilisin Carlsberg with boronic acids.
    Seufer-Wasserthal P, Martichonok V, Keller TH, Chin B, Martin R, Jones JB.
    Bioorg Med Chem; 1994 Jan 17; 2(1):35-48. PubMed ID: 7922119
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  • 13. Prolyl endopeptidase catalysis. A physical rather than a chemical step is rate-limiting.
    Polgár L.
    Biochem J; 1992 May 01; 283 ( Pt 3)(Pt 3):647-8. PubMed ID: 1590752
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  • 16. Alkaline protease catalysis of a secondary amine to form a peptide bond.
    Chen ST, Kao CL, Wang KT.
    Int J Pept Protein Res; 1995 May 01; 46(3-4):314-9. PubMed ID: 8537185
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  • 17. Use of methyl iodide for probing the polarity of the immediate environment of --SH groups in thiolenzymes. Reaction of methyl iodide with thiosubtilisin.
    Halász P, Polgár L.
    Eur J Biochem; 1976 Dec 11; 71(2):563-9. PubMed ID: 1009966
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  • 20. A new substrate and two inhibitors applicable for thermitase, subtilisin BPN' and alpha-chymotrypsin. Comparison of kinetic parameters with customary substrates and inhibitors.
    Brömme D, Fittkau S.
    Biomed Biochim Acta; 1985 Dec 11; 44(7-8):1089-94. PubMed ID: 3910035
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