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Journal Abstract Search

91 related items for PubMed ID: 4671999

  • 1. Symmetry and asymmetry in the mechanisms of hydrolysis by serine proteases and their thiol analogues.
    Polgár L.
    Acta Biochim Biophys Acad Sci Hung; 1972; 7(4):319-34. PubMed ID: 4671999
    [No Abstract] [Full Text] [Related]

  • 2. Effect of ionic strength of the steady-state kinetics of -chymotrypsin-catalyzed reactions.
    Martinek K, Yatsimirskii AK, Berezin IV.
    Mol Biol; 1971; 5(1):77-88. PubMed ID: 5154806
    [No Abstract] [Full Text] [Related]

  • 3. Deuterium isotope effects on acylation of subtilisin.
    Polgár L.
    Biochim Biophys Acta; 1973 Oct 10; 321(2):639-42. PubMed ID: 4762412
    [No Abstract] [Full Text] [Related]

  • 4. Subtilisin-catalyzed hydrolysis of peptide methyl esters.
    Philipp M, Bender ML.
    FEBS Lett; 1974 Jun 15; 42(3):282-4. PubMed ID: 4854515
    [No Abstract] [Full Text] [Related]

  • 5. Specificities of alpha-chymotrypsin and subtilisin Carlsberg. The alpha-acylamido effect in beta-phenylpropionates and their rigid analogs.
    Matta MS, Staley DD.
    J Biol Chem; 1974 Feb 10; 249(3):732-7. PubMed ID: 4811900
    [No Abstract] [Full Text] [Related]

  • 6. Kinetic manifestations of the structure of the active center of -chymotrypsin on interacting with fragments of specific substrates.
    Martinek K, Varfolomeev SD, Levashov AV, Berezin IV.
    Mol Biol; 1971 Feb 10; 5(3):278-86. PubMed ID: 5154822
    [No 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 03; 12(14):2559-66. PubMed ID: 4711463
    [No Abstract] [Full Text] [Related]

  • 8. N-[2,2-dimethyl-3-(N-(4-cyanobenzoyl)amino)nonanoyl]-L-phenylalanine ethyl ester as a stable ester-type inhibitor of chymotrypsin-like serine proteases: structural requirements for potent inhibition of alpha-chymotrypsin.
    Iijima K, Katada J, Yasuda E, Uno I, Hayashi Y.
    J Med Chem; 1999 Jan 28; 42(2):312-23. PubMed ID: 9925737
    [Abstract] [Full Text] [Related]

  • 9. Enzymatic resolution of amino acids via ester hydrolysis.
    Miyazawa T.
    Amino Acids; 1999 Jan 28; 16(3-4):191-213. PubMed ID: 10399013
    [Abstract] [Full Text] [Related]

  • 10. Kinetics and mechanism of proteinase-binding of pregnancy zone protein (PZP). Appearance of sulfhydryl groups in reactions with proteinases.
    Christensen U, Sottrup-Jensen L, Simonsen M.
    J Enzyme Inhib; 1992 Jan 28; 5(4):269-79. PubMed ID: 1285248
    [Abstract] [Full Text] [Related]

  • 11. Specificity of -chymotrypsin. The -chymotrypsin-catalyzed hydrolysis of N-acylamino acid p-nitrophenyl esters.
    Béchet JJ, Dupaix A, Roucous C.
    Biochemistry; 1973 Jul 03; 12(14):2566-72. PubMed ID: 4711464
    [No Abstract] [Full Text] [Related]

  • 12. The reactivity of thiol-subtilisin, an enzyme containing a synthetic functional group.
    Polgar L, Bender ML.
    Biochemistry; 1967 Feb 03; 6(2):610-20. PubMed ID: 6047645
    [No Abstract] [Full Text] [Related]

  • 13. Comparison of the active sites of atropinesterase and some serine proteases by spin-labeling.
    van der Drift AC, Moes GW, van der Drift E, Rousseeuw BA.
    Biochemistry; 1985 Sep 24; 24(20):5333-42. PubMed ID: 3000432
    [Abstract] [Full Text] [Related]

  • 14. On the stereochemistry of catalysis by serine proteases.
    Polgár L, Asbóth B.
    J Theor Biol; 1974 Aug 24; 46(2):543-58. PubMed ID: 4420762
    [No Abstract] [Full Text] [Related]

  • 15. Increase in the susceptibility of hemoglobin to proteases upon treatment with p-mercuribenzoate.
    Kimura H, Yamato S, Murachi T.
    J Biochem; 1978 Jul 24; 84(1):205-11. PubMed ID: 690099
    [Abstract] [Full Text] [Related]

  • 16. Investigation of a general base mechanism for ester hydrolysis in C-C hydrolase enzymes of the alpha/beta-hydrolase superfamily: a novel mechanism for the serine catalytic triad.
    Li JJ, Bugg TD.
    Org Biomol Chem; 2007 Feb 07; 5(3):507-13. PubMed ID: 17252134
    [Abstract] [Full Text] [Related]

  • 17. Proceedings: Flourescence of beta-lactoglobulin B as a function of pH before and after blocking of the thiol groups with organomercurials.
    Préaux G, Dekoster H.
    Hoppe Seylers Z Physiol Chem; 1974 Oct 07; 355(10):1238-9. PubMed ID: 4461573
    [No Abstract] [Full Text] [Related]

  • 18. On the rational design of substrate mimetics: The function of docking approaches for the prediction of protease specificities.
    Günther R, Elsner C, Schmidt S, Hofmann HJ, Bordusa F.
    Org Biomol Chem; 2004 May 21; 2(10):1442-6. PubMed ID: 15136799
    [Abstract] [Full Text] [Related]

  • 19. Thionesters as a probe for electrophilic catalysis in the serine protease mechanism.
    Campbell P, Nashed NT, Lapinskas BA, Gurrieri J.
    J Biol Chem; 1983 Jan 10; 258(1):59-66. PubMed ID: 6336754
    [Abstract] [Full Text] [Related]

  • 20. Serine proteases: structure and mechanism of catalysis.
    Kraut J.
    Annu Rev Biochem; 1977 Jan 10; 46():331-58. PubMed ID: 332063
    [No Abstract] [Full Text] [Related]

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