The influence of the geometric properties of the active centre on the specificity of α‐chymotrypsin catalysis
Authors:
- 1 June 1972
- journal article
- Published by Wiley in FEBS Letters
- Vol. 23 (1) , 122-124
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- On the relationship between structure and reactivity of α‐chymotrypsin substratesFEBS Letters, 1971
- Separation of polar, steric and specific effects in the α-chymotrypsin-catalyzed hydrolysis of acyl-substituted p-nitrophenyl estersBiochemical and Biophysical Research Communications, 1970
- α-Chymotrypsin: A Case Study of Substituent Constants and Regression Analysis in Enzymic Structure—Activity RelationshipsJournal of Pharmaceutical Sciences, 1970
- Structure of crystalline α-chymotrypsinJournal of Molecular Biology, 1969
- Steric Effects in the Deacylation of Acyl-Chymotrypsins*Biochemistry, 1967
- Substrate Hydrophobic Groups and the Maximal Rate of Enzyme ReactionsNature, 1967
- The Primary Specificity of α-Chymotrypsin. Acylated Amino Acid Esters with Normal Alkyl Side Chains1Journal of the American Chemical Society, 1965