Evidence map›Paper›PMID 42488464›Full record

ReviewChemical science2026

Methods for the establishment of enzymatic mechanisms - from QM to ML.

Rui P P Neves, João T S Coimbra, Pedro Paiva, Umberto Raucci, Sudip Das, Ana R Calixto, António J M Ribeiro, João P M Sousa, Pedro Ferreira, Enrico Trizio and 3 more

Abstract readReview
In one paragraph

Review in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Rui P P NevesLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0003-2032-9308
João T S CoimbraLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0001-9138-7498
Pedro PaivaLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0002-7003-6055
Umberto RaucciItalian Institute of Technology Genova GE 16163 Italy michele.parrinello@iit.it.ORCID https://orcid.org/0000-0002-8219-224X
Sudip DasItalian Institute of Technology Genova GE 16163 Italy michele.parrinello@iit.it.
Ana R CalixtoLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0002-1123-0413
António J M RibeiroLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0002-2533-1231
João P M SousaLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0002-4915-4946
Pedro FerreiraLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0001-7015-5460
Enrico TrizioItalian Institute of Technology Genova GE 16163 Italy michele.parrinello@iit.it.ORCID https://orcid.org/0000-0003-2042-0232
Pedro A FernandesLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0003-2748-4722
Michele ParrinelloItalian Institute of Technology Genova GE 16163 Italy michele.parrinello@iit.it.ORCID https://orcid.org/0000-0001-6550-3272
Maria J RamosLAQV, REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto Rua do Campo Alegre s/n Porto 4169-007 Portugal mjramos@fc.up.pt.ORCID https://orcid.org/0000-0002-7554-8324

Funding

COMPUTER AIDED ANALYSIS OF ELECTROCARDIOGRAPHYZ01CT000002 · CIT · COMPUTER RESEARCH AND TECHNOLOGY · PI BAILEY, JAMES J. · 1985 to 2003
–
Intramural NIH HHS Z01 CT000002
6 · The paper itself

Abstract

We offer a practical and conceptual introduction to some of the current approaches to modelling enzymatic reaction mechanisms, ranging from quantum mechanics (QM), molecular mechanics (MM), and hybrid QM/MM approaches to enhanced sampling methods, knowledge-based approaches, and machine learning (ML) advances. We discuss how static and dynamic QM/MM approaches, as well as multi-PES strategies, have contributed to understanding the role of conformational diversity, electrostatic preorganization and solvent participation in the determination of catalytic barriers and reaction paths. We focus on how advanced sampling techniques and data-driven collective variables have enabled the exploration of rare events and reaction coordinates, as well as how knowledge- and rule-based approaches have facilitated the interpretation and hypothesis generation for different families of enzymes. Recent developments in ML potentials, ML collective variables, and committor-based sampling are presented as innovative methods that have been able to address some of the current challenges in accuracy, sampling efficiency, and the identification of low-dimensional representations of reaction coordinates. A case study of α-amylase demonstrates how the combination of these strategies leads to a comprehensive understanding of enzyme reactivity, from the chemical to the conformational level. Collectively, these developments contribute to a predictive understanding of enzymatic catalysis, which will have extensive implications in enzyme engineering, sustainable chemistry, and drug discovery. Advances in high performance computing, automated simulation pipelines and data formats will likely make multiscale simulation more accessible and reproducible. Simultaneously, the combined application of mechanistic knowledge, ML, and experimental validation will hopefully advance the discovery and optimization of biocatalysts with well-defined properties, tailored to meet pressing societal needs, such as plastic biodegradation, carbon sequestration, sustainable synthesis and personalised medicine.

Identifiers

PMID42488464
PMCPMC13389585

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.