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1	Studies of immobilized and cross-linked a[alpha]-chymotrypsin to explore solvent stabilization / Bassett, Paul M. January 1995 (has links) Thesis (M.S.)--Youngstown State University, 1995. / Includes bibliographical references (p. [115]-[121]). Chymotrypsin.
2	A molecular modelling study of the catalytic activity of [alpha]-chymotrypsin Krug, Russell Roland, January 1976 (has links) Thesis--Wisconsin. / Vita. Includes bibliographical references (leaves 217-235). Chymotrypsin.
3	Linking of FTIR data to structure : application to cinnamoyl serine proteases and gramicidin D Booth, Victoria Kaye January 2001 (has links) No description available. 572.76 Chymotrypsin
4	Towards an #alpha#-chymotrypsin mimic and the 3-acetyltetramic acid erythroskyrine Tankard, M. January 1989 (has links) No description available. 572 Chymotrypsin enzymes
5	Cloning and functional expression of Taiwan cobra chymotrypsin inhibitor Cheng, Yun-Ching 20 June 2003 (has links) Previous studies showed that dendrotoxins and B chain of b-Bungarotoxin shared sequence and structural homology with Kunitz-type protease inhibitors. In the present study, the cDNA of Kunitz¡Vtype protease inhibitor was successfully amplified from Taiwan cobra venom gland total RNAs using the primers designed from the B chain of b-Bungarotoxin. The deduced amino acid sequence of the cDNA exhibited the structural character of chymotrypsin inhibitor, and the mature protein contained 57 amino acids with six Cys residues. The chymotrypsin inhibitor was subcloned into pET29a(+) and transformed into BL21(DE3) E.coli strain. The expressed protein was isolated from inclusion bodies of E.coli and subjected to refolding into its folded structure. The inhibitor potency of the recombinant protein on chymotrypsin activity had a Ki value of 461.3 mM. However, removal of its N-terminal fused peptide with thrombin further increased the Ki value to 31.7 mM. Removal of the N-terminal residues further reduced its inhibitory potency, and the inhibitory activity completely lost after deleting three residues at the N-terminus of mature protein. This reflects that the N-terminal region of protease inhibitor should be associated with its activity. The genomic DNA encoding the precursor of the inhibitor was also amplified using PCR. The genetic structure composed of three exons and three introns, which shared the same organization with the b-Bungarotoxin B chain gene. Moreover, the two genes showed a high degree of sequence identity up to 83%. This observation emphasizes the idea that the B chain of b-Bungarotoxin and protease inhibitor are evolutionarily related. taiwan cobra chymotrypsin inhibitor
6	An investigation of chymotrypsin A[gamma]inhibition with peptide aldehydes and related analogs ; II Inhibition of elastase by tetrapeptide chloromethyl ketones Whitley, Ronald Jay 12 1900 (has links) No description available. Enzyme inhibitors Chymotrypsin
7	I Inhibition of elastase by peptide chloromethyl ketones II Modification of chymotrypsin by an aryl cyanate reagent Tuhy, Peter Mirko 05 1900 (has links) No description available. Enzymes Enzyme inhibitors Chymotrypsin
8	An ultracentrifuge study of self-associating protein systems Fennell, David John January 1971 (has links) iii, 136 leaves : ill. ; 26 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.) from the Dept. of Physical and Inorganic Chemistry, University of Adelaide, 1972 Chymotrypsin. Insulin. Sedimentation analysis.
9	An ultracentrifuge study of self-associating protein systems. Fennell, David John. January 1971 (has links) (PDF) Thesis (Ph.D.) from the Dept. of Physical and Inorganic Chemistry, University of Adelaide, 1972.
10	Studies on the mechanism of action of proteolytic enzymes Hawkins, M. J. January 1965 (has links) No description available.

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