ArticleProtein science : a publication of the Protein Society2026
pLM-Repeat: Exploiting the sequence representations of protein language models for sensitive repeat detection.
Article in Protein science : a publication of the Protein Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- pLM-Repeat: Exploiting the sequence representations of protein language models for sensitive repeat detection.Protein science : a publication of the Protein Society · 2026Article
- Diversity and structural-functional insights of alpha-solenoid proteins.Protein science : a publication of the Protein Society · 2024Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Duplication is an essential mechanism of molecular evolution, which operates across biological scales, from whole genomes to single basepairs. Its study is central to understanding protein evolution, but the detection of duplication events often becomes challenging over evolutionary time, due to the accumulating sequence divergence. The most sensitive sequence-based protein repeat detection method, HHrepID, relies on the construction of multiple sequence alignments (MSAs) to enhance statistical signals of internal similarity and thus facilitate the detection of ancient duplications. However, such an alignment-based approach comes at the expense of speed, severely limiting its applicability to large-scale scans. Recent advances in protein representation learning have introduced sequence embeddings extracted from protein language models (pLMs) as a powerful and faster alternative to MSAs. Such representations have been shown to be effective in detecting distant sequence similarity, as exemplified by the pLM-BLAST software developed in our group. In this study, we describe pLM-Repeat, a pipeline built on top of pLM-BLAST to identify repeat patterns encoded in sequence representations. pLM-Repeat achieves comparable sensitivity to HHrepID in detecting the presence of repeats, while identifying many more repeat units and providing shorter runtimes, allowing us to detect novel repeat proteins in the AlphaFold Protein Structure Database with the aid of a pre-filtering model trained on repeat protein representations. pLM-Repeat is available as an open-source tool at https://github.com/KYQiu21/plmrepeat.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.