Evidence map›Paper›PMID 42775364›Full record

ArticleBioinformatics advances2026

EnzymeSifter: a tool for discovery of industrial enzymes from metagenomes.

Omar Darawsheh, Matthew Bashton

Abstract read
In one paragraph

Article in Bioinformatics advances, 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

2 authors.

Omar DarawshehSchool of Geography and Natural Sciences, Faculty of Science and Engineering, Northumbria University, Newcastle upon Tyne, NE1 8ST, United Kingdom.ORCID https://orcid.org/0009-0002-9416-9589
Matthew BashtonSchool of Geography and Natural Sciences, Faculty of Science and Engineering, Northumbria University, Newcastle upon Tyne, NE1 8ST, United Kingdom.ORCID https://orcid.org/0000-0002-6847-1525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Summary: Metagenomes contain vast amounts of sequences, complicating the process of identifying candidate enzymes for industrial applications. Industrial applications require evaluating multiple biochemical properties simultaneously, including solubility, thermal stability, and pH. While separate predictors for each property exist, a score that combines multiple predicted values will be more descriptive than those generated individually by distinct tools. We present EnzymeSifter, a tool that automates enzyme discovery from vast metagenomes and enables multi-property predictions. It identifies the best performing enzymes using a computed composite score of all predicted values and generates a phylogenetic tree to select the top candidate from each clade-ensuring diversity and even sampling of sequence space. It acts as a sieve that filters according to the user inputs and keeps the most promising non-redundant enzymes for experimental validation. Availability and implementation: EnzymeSifter is freely available and released under an MIT licence. EnzymeSifter source code is available at https://github.com/Bashton-Lab/EnzymeSifter.

Identifiers

PMID42775364
PMCPMC13597120

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.