✦ LIBER ✦

Preferential binding of competitive inhibitors to the monomeric form of α-chymotrypsin

✍ Scribed by Nichol, L. W.; Jackson, W. J. H.; Winzor, D. J.

Book ID: 126306206
Publisher: American Chemical Society
Year: 1972
Tongue: English
Weight: 897 KB
Volume: 11
Category: Article
ISSN: 0006-2960
DOI: 10.1021/bi00754a017

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Effect of dioxane on the binding of comp

Effect of dioxane on the binding of competitive inhibitor proflavin and catalytic activity of bovine pancreatic α-chymotrypsin

✍ V. A. Sirotkin; T. A. Mukhametzyanov; Yu. V. Karmanova 📂 Article 📅 2007 🏛 International Academic Publishing Co (Nauka/Interp 🌐 English ⚖ 192 KB

Immunological aspects of the binding of

Immunological aspects of the binding of substrate analogues and polypeptide inhibitors to α-chymotrypsin

✍ Enrico Bucci; Donald E. Bowman 📂 Article 📅 1970 🏛 Elsevier Science ⚖ 718 KB

The Effect of Competitive Inhibitors on

The Effect of Competitive Inhibitors on the Milk Clotting Activity of α-Chymotrypsin 1

✍ Huang, H. T.; Niemann, Carl 📂 Article 📅 1951 🏛 American Chemical Society 🌐 English ⚖ 291 KB

Binding of competitive inhibitors to δ-c

Binding of competitive inhibitors to δ-chymotrypsin in the alkaline pH region. Competitive inhibition kinetics and proton-uptake measurements

✍ Valenzuela, Pablo; Bender, Myron L. 📂 Article 📅 1970 🏛 American Chemical Society 🌐 English ⚖ 717 KB

Calorimetric investigations of the bindi

Calorimetric investigations of the binding of inhibitors to α-chymotrypsin. I. Enthalpy of dilution of α-chymotrypsin and of proflavine, and the enthalpy of binding of indole, N-acetyl-D-tryptophan, and proflavine to α-chymotrypsin

✍ Shiao, Daniel D. F.; Sturtevant, Julian M. 📂 Article 📅 1969 🏛 American Chemical Society 🌐 English ⚖ 719 KB

Peptidyl epoxides as inhibitors of α-chy

Peptidyl epoxides as inhibitors of α-chymotrypsin: Remarkable change from irreversible to reversible competitive inhibitor as a consequence of the improvement of binding affinity

✍ Dong H. Kim; Zhi-Hong Li; Soo Suk Lee 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 200 KB

The replacement of the ester group in (23,3R)-2-benzyl-3,4-epoxybutanoic acid methyl ester (1) with a N-benzoyl-2-pyrrolidylcarboxamide moiety changes the mode of inhibition for a-chymotrypsin from an active site directed inactivator to a reversible competitive inhibitor.