The Primary Specificity of α-Chymotrypsin. Acylated Amino Acid Esters with Normal Alkyl Side Chains

J. Bryan Jones, Toyoki Kunitake, Carl Niemann, George E. Hein

研究成果: ジャーナルへの寄稿学術誌査読

45 被引用数 (Scopus)

抄録

The α-chymotrypsin-catalyzed hydrolysis of a series of N-acetyl-L-amino acid esters of the general formula CH3CONHCH[(CH2)nH]CO2CH3, where n=1-6, has been examined. For this series, K0 reaches a minimum and k0 a maximum when n=5. The method of interaction of acylated L-amino acid derivatives with chymo-trypsin is discussed as well as the magnitude of the forces which can be attributed to the side chain. Each additional methylene group up to the optimum number contributes approximately 680-790 cal. to increased substrate binding and 500 cal. toward decreasing the free energy of activation of the rate-determining kinetic step. The data are incorporated into a general correlation between structure and a-chymotrypsin specificity.

本文言語英語
ページ(範囲)1777-1781
ページ数5
ジャーナルJournal of the American Chemical Society
87
8
DOI
出版ステータス出版済み - 1月 1 1965
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 触媒
  • 化学 (全般)
  • 生化学
  • コロイド化学および表面化学

フィンガープリント

「The Primary Specificity of α-Chymotrypsin. Acylated Amino Acid Esters with Normal Alkyl Side Chains」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル