Related Experiment Video
Updated: Jan 14, 2026

Modeling an Enzyme Active Site using Molecular Visualization Freeware
Published on: December 25, 2021
Multiscale Modeling of Enzymatic Efficiency in Multienzyme Complex: Effect of Interenzyme Distance, Crowding Effect
Parisa Fasihianifard1, Kingsley Y Wu1, Shivansh Kaushik1
1Department of Chemistry, University of California, Riverside, Riverside, California 92521, United States.
Abstract:
Molecular association is one of the most fundamental principles of chemistry and biology. Biomolecular complexes need to colocalize sequential catalytic and chemical processes such that the intermediates are precisely positioned to diffuse efficiently. The relative distance and orientation between the active sites within these complexes may affect the intermediate binding, which may also be different under different cell environments. In this work, we used Brownian dynamics simulations to model an intermediate substrate association in the tryptophan biosynthesis pathway in Escherichia coli (E. coli) for investigating potential advantages of using TrpCF bifunctional enzyme which fuses phosphoribosyl anthranilate isomerase (PRAI) and indoleglycerol phosphate synthase (IGPS). We focused on transporting a product of PRAI, 1-(o-carboxyphenylamino)-1-deoxyribulose 5-phosphate (CdRP), which is also the substrate of in IGPS. We report the average association time and direct binding percentage when the substrate concentration is 10.0 μM as an estimated physiological concentration in cells. Our results suggest that final product synthesis efficiency can be achieved by optimizing the interenzyme distance and by properly aligning the orientation of the active sites. In addition, the intermolecular interactions between the substrate and macromolecule crowders largely affected the transportation of a substrate. The overall rate of product synthesis enhancement in a multienzyme complex depends on the distance between enzymes when the substrate leaking phenomenon exists. Our work highlights the importance of the enzyme spatial organization in regulating the production efficiency of a product in multienzyme complexes, broadens implications in synthesis processes under complex cell environments, and brings biophysical insights into the enzyme-substrate association and understanding of target ligand/substrate kinetics.
More Related Videos
Related Concept Videos
Enzyme Kinetics
Scientists typically study enzyme kinetics with a fixed amount of enzyme in the controlled environment of a test tube. When more reactant, or substrate, is...
Introduction to Mechanisms of Enzyme Catalysis
Introduction to Enzyme Kinetics
The experimenter can then plot the initial reaction rate or velocity (Vo) of a given trial against the substrate concentration ([S]) to obtain a graph of the reaction properties. For many enzymatic reactions involving a...
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...
Enzymes
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
Cooperative Allosteric Transitions

