Related Experiment Video
Updated: Aug 15, 2026

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
Published on: January 16, 2016
The catalytic mechanism of alpha-amylases based upon enzyme crystal structures and model building calculations
1Pacific Institute of Bioorganic Chemistry, Russian Academy of Sciences, Vladivostok.
Abstract:
Based upon the known crystal structures of Taka-amylase A and the recently refined Porcine pancreatic alpha-amylase inhibitor complex a mechanism of catalysis in amylase active centers is proposed. The mechanism differs significantly from the well-known lysozyme model of catalysis. The hydrolysis is catalyzed by three carboxyl groups and its starts from a water nucleophilic attack and opening of the glucose ring in the catalytic center rather than from protonation of the glycosidic oxygen. The main supporting experimental observations are briefly discussed.
Related Concept Videos
Induced-fit Model
Enzymes exhibit substrate specificity, meaning that they can only bind to certain substrates. This is mainly determined by the shape and chemical characteristics of...
Enzymes
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
Introduction to Mechanisms of Enzyme Catalysis
Allosteric Proteins-ATCase
Aspartate transcarbamoylase (ATCase) is a cytosolic enzyme that catalyzes the condensation of L-aspartate and carbamoyl phosphate to N-carbamoyl-L-aspartate. This reaction is the first step in pyrimidine biosynthesis. UTP and CTP, the end products of the pyrimidine synthesis pathway,...
Protein Organization
The primary structure of a protein is its amino acid sequence.
Introduction to Mechanisms of Enzyme Catalysis

