Evidence map›Paper›PMID 42881161›Full record

ArticleNature communications2026

Iterative and data-driven ortholog mining enables reliable discovery of stereoselective ketoreductases.

Peter Stockinger, Michael Niklaus, Kevin M Yar, Nicolas Imstepf, Ivana Pastierikova, Jasmin Küng, Steven Hanlon, Hans Iding, Sumire Honda Malca, Rebecca Buller

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

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Peter Stockinger *Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.
Michael Niklaus *Institute of Chemistry and Biotechnology, Zurich University of Applied Sciences, Wädenswil, Switzerland.ORCID http://orcid.org/0000-0003-4713-261X
Kevin M YarInstitute of Chemistry and Biotechnology, Zurich University of Applied Sciences, Wädenswil, Switzerland.
Nicolas ImstepfDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0009-0008-0723-8528
Ivana PastierikovaInstitute of Chemistry and Biotechnology, Zurich University of Applied Sciences, Wädenswil, Switzerland.
Jasmin KüngInstitute of Chemistry and Biotechnology, Zurich University of Applied Sciences, Wädenswil, Switzerland.
Steven HanlonProcess Chemistry and Catalysis, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, Basel, Switzerland.
Hans IdingProcess Chemistry and Catalysis, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, Basel, Switzerland.
Sumire Honda MalcaInstitute of Chemistry and Biotechnology, Zurich University of Applied Sciences, Wädenswil, Switzerland.
Rebecca BullerDepartment of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland. rebecca.buller@unibe.ch.ORCID http://orcid.org/0000-0002-5997-1616

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) 225147
6 · The paper itself

Abstract

Ketoreductases (KREDs) enable stereoselective alcohol synthesis and are widely used industrially. Yet identifying process-compatible and selective enzymes for non-native substrates remains challenging, requiring extensive screening. Here, we present an iterative ortholog mining strategy to explore functional space. Starting from a known KRED, we sample its orthogroup across 48 evolutionarily distant variants, identifying five enzymes producing pharmaceutically relevant alcohols (de/ee 42.8% to >99%). Refined sampling of 60 phylogenetically close orthologs yields further improved ketoreductases (de/ee 98% to >99%). Because ortholog mining is genome-dependent, it overlooks enzymes from unsequenced organisms. To address this, we use our dataset to explore homologous KREDs beyond the sampled orthogroup, expanding the search space fifteenfold. To this end, we develop the automated pipeline HomoLogic, whose functional descriptors, fed into interpretable models, predict KRED performance accurately (R² up to 0.76). Overall, we show that evolutionarily balanced ortholog panels combined with data-driven modeling enable efficient discovery of stereoselective biocatalysts.

Indexed as

Alcohol OxidoreductasesData MiningAlcoholsPhylogenyStereoisomerismSubstrate SpecificityAlcohol OxidoreductasesAlcohols

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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.