Off the beaten (catalytic) path: Charting the mechanistic space of enzyme reactions

A António J. M. Ribeiro (LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências da Universidade do Porto 1 , 4169-007 Porto,) P Pedro A. Fernandes (LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências da Universidade do Porto 1 , 4169-007 Porto,) M Maria J. Ramos (LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências da Universidade do Porto 1 , 4169-007 Porto,)

Abstract

Do enzymes always follow a single linear path of catalytic steps? Or is the catalytic process more like a maze of forest trails? Enzyme mechanisms are typically presented as a linear (or circular) sequence of chemical steps, and most mechanistic studies aim to identify “the” correct catalytic pathway. Alternative proposals are often pitted against one another and sometimes fiercely debated. In this paper, we consider the possibility that the reaction mechanism space accessible to enzyme active sites is more diverse than commonly recognized. This mechanistic space can be conveniently represented as a graph, where nodes correspond to active-site configurations (reactants, intermediates, or products) and edges denote catalytic steps transforming one configuration into another. We show that it is possible to generate alternative mechanism proposals, which take into account the 3D coordinates of the active site and known catalytic rules, for more than half of a test set of 25 enzymes. These findings hint at a previously unexplored facet of enzyme catalysis and underscore the need for the systematic exploration of the complete reactional space in computational studies of enzyme mechanisms.

Article Details

Volume / Issue Vol. 163, Issue 13
Published October 07, 2025
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (3)

A

António J. M. Ribeiro

LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências da Universidade do Porto 1 , 4169-007 Porto,

P

Pedro A. Fernandes

LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências da Universidade do Porto 1 , 4169-007 Porto,

M

Maria J. Ramos

LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências da Universidade do Porto 1 , 4169-007 Porto,