Evidence map›Paper›PMID 42799051›Full record

ArticleDigital discovery2026

Pockets to products: a data-driven approach for classification of monoterpene synthases.

Cathal Ó Raghallaigh, Nigel S Scrutton, Sam Hay

Abstract read
In one paragraph

Article in Digital discovery, 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

3 authors.

Cathal Ó RaghallaighManchester Institute of Biotechnology, Department of Chemistry, The University of Manchester 131 Princess Street Manchester M1 7DN UK Sam.Hay@manchester.ac.uk.ORCID https://orcid.org/0000-0001-6431-1316
Nigel S ScruttonManchester Institute of Biotechnology, Department of Chemistry, The University of Manchester 131 Princess Street Manchester M1 7DN UK Sam.Hay@manchester.ac.uk.ORCID https://orcid.org/0000-0002-4182-3500
Sam HayManchester Institute of Biotechnology, Department of Chemistry, The University of Manchester 131 Princess Street Manchester M1 7DN UK Sam.Hay@manchester.ac.uk.ORCID https://orcid.org/0000-0003-3274-0938

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoterpene synthases (mTSs) are a large family of enzymes, which have promising industrial applications, yet remain difficult to engineer due to complex and poorly understood sequence-function relationships. Here, we present a structure-based machine learning (ML) framework that accurately predicts whether a mTS is likely to produce linalool or limonene, chosen as canonical examples of linear and cyclic monoterpene products, respectively. Our approach identifies active site properties, which are used as ML features, enabling functional predictions that go beyond sequence alone. As residue positioning is important for monoterpene synthesis, we created an algorithm to identify structurally conserved residues in the active sites of mTSs, identifying new and existing motifs essential for both general catalysis and specific cyclisation steps. This integrated workflow thus provides insights into terpene synthases that were previously inaccessible and may offer a generalizable strategy for probing and engineering other poorly understood enzyme families. Future work could see this approach used to guide the rational design of mTSs and other hard-to-engineer enzyme families.

Identifiers

PMID42799051
PMCPMC13613485

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.