ArticleAmino acids2026
PCLPred: identifying plant chloride transport-related proteins using reduced amino acid alphabets and N-peptide composition.
Article in Amino acids, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
Abstract
Chloride transport-related proteins play critical roles in coordinating ion cycling, maintaining cellular homeostasis, and enabling plants to dynamically adapt to environmental changes, particularly under salt stress conditions. Given the rapid accumulation of protein sequence data, the experimental identification of proteins is time-consuming and expensive. Therefore, efficient computational methods are urgently needed as a practical supplement to experimental research. Here, we present PCLPred, an SVM-based predictor that integrates reduced amino acid alphabets with N-peptide composition to represent protein sequences. We systematically evaluated 673 reduction schemes and selected an optimal encoding strategy for model training. PCLPred demonstrated superior performance compared to baseline models, achieving an overall accuracy of 95.10% and an AUC of 0.981 in nested cross-validation. Altogether, PCLPred provides an efficient and reliable tool for high-throughput screening of candidate plant chloride transport-related proteins, facilitating functional annotation and experimental validation.
Indexed as
Identifiers
What Socratic 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 Socratic graph.