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3. Alkylation of serine at the active site of trypsin. Lawson WB; Leafer MD; Tewes A; Rao GJ Hoppe Seylers Z Physiol Chem; 1968 Feb; 349(2):251-62. PubMed ID: 5677011 [No Abstract] [Full Text] [Related]
4. Thermodynamics of the hydrophobic interaction in the active center of trypsin. Investigation with amidines and guanidines. Mares-Guia M; Figueiredo AF Biochemistry; 1970 Aug; 9(16):3223-7. PubMed ID: 5489774 [No Abstract] [Full Text] [Related]
5. STUDIES ON THE ACTIVE CENTER OF TRYPSIN. THE BINDING OF AMIDINES AND GUANIDINES AS MODELS OF THE SUBSTRATE SIDE CHAIN. MARES-GUIA M; SHAW E J Biol Chem; 1965 Apr; 240():1579-85. PubMed ID: 14285494 [No Abstract] [Full Text] [Related]
6. Pseudotrypsin. A modified bovine trypsin produced by limited autodigestion. Smith RL; Shaw E J Biol Chem; 1969 Sep; 244(17):4704-12. PubMed ID: 5817636 [No Abstract] [Full Text] [Related]
7. Irreversible enzyme inhibitors. CXLIV. Proteolytic enzymes. VII. Additonal active-site-directed irreversible inhibitors of trypsin derived from m- and p-(phenoxyalkoxy)benzamidines with a terminal sulfonyl fluoride. Baker BR; Erickson EH J Med Chem; 1969 Jan; 12(1):112-7. PubMed ID: 5763005 [No Abstract] [Full Text] [Related]
8. Trypsin substrates derived from benzamidine: application to active site titration and isolation of acyl-enzyme intermediate. Tanizawa K; Ishii SI; Kanaoka Y Biochem Biophys Res Commun; 1968 Sep; 32(5):893-7. PubMed ID: 5682313 [No Abstract] [Full Text] [Related]
9. Hydrophobic interactions in the trypsin active center. The sensitivity of the hydrophobic binding site to side chain modifications in competitive inhibitors of the amidinium type. Mares-Guia M Arch Biochem Biophys; 1968 Sep; 127(1):317-22. PubMed ID: 5697989 [No Abstract] [Full Text] [Related]
10. The specific inactivation of trypsin by ethyl p-guanidinobenzoate. Mares-Guia M; Shaw E J Biol Chem; 1967 Dec; 242(23):5782-8. PubMed ID: 6073660 [No Abstract] [Full Text] [Related]
11. Irreversible enzyme inhibitors. CXV. Proteolytic enzymes. V. Active-site-directed irreversible inhibitors of trypsin derived from p-(phenoxyalkoxy) benzamidines with a terminal sulfonyl fluoride. Baker BR; Erickson EH J Med Chem; 1968 Mar; 11(2):245-9. PubMed ID: 5654210 [No Abstract] [Full Text] [Related]
12. Modification of carboxyl groups in the binding sites of trypsin with the Meerwein reagent. Nakayama H; Tanizawa K; Kanaoka Y Biochem Biophys Res Commun; 1970 Aug; 40(3):537-41. PubMed ID: 5492151 [No Abstract] [Full Text] [Related]
14. Chemical modifications of amino groups of trypsin. Nureddin A; Inagami T Biochem Biophys Res Commun; 1969 Sep; 36(6):999-1005. PubMed ID: 5344729 [No Abstract] [Full Text] [Related]
15. The location of the active-site histidine residue in the primary sequence of papain. Husain SS; Lowe G Biochem J; 1968 Aug; 108(5):861-6. PubMed ID: 5673531 [TBL] [Abstract][Full Text] [Related]
17. Phenacyl bromides as chromophoric reagents for alpha-chymotrypsin. Sigman DS; Torchia DA; Blout ER Biochemistry; 1969 Nov; 8(11):4560-6. PubMed ID: 5353114 [No Abstract] [Full Text] [Related]
18. [Synthetic inhibitors of serine proteinases. 35. Inhibition action of amidino- and guanidinophenyl derivatives against hemolysis initiated by complement activation]. Hoffmann A; Markwardt F Pharmazie; 1989 Feb; 44(2):141-4. PubMed ID: 2748697 [TBL] [Abstract][Full Text] [Related]
19. Studies on the active center of trypsin. Further characterization of the hydrophobic binding site. Mares-Guia M; Shaw E; Cohen W J Biol Chem; 1967 Dec; 242(23):5777-81. PubMed ID: 6073659 [No Abstract] [Full Text] [Related]
20. Multimolecular species of trypsin. Hakim AA Enzymologia; 1972 Jan; 42(1):45-64. PubMed ID: 5061878 [No Abstract] [Full Text] [Related] [Next] [New Search]