Evidence map›Paper›PMID 37462277›Full record

ArticleGenetics2023

Clusters of acidic and hydrophobic residues can predict acidic transcriptional activation domains from protein sequence.

Sanjana R Kotha, Max Valentín Staller

Abstract read
In one paragraph

Article in Genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
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  6. International journal of molecular sciences · 2026
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  16. The potent PHL4 transcription factor effector domain contains significant disorder.Protein science : a publication of the Protein Society · 2024
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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.

Sanjana R KothaDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Max Valentín StallerDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

Funding

Defining the protein sequence features that control transcriptional activation domain functionR35GM150813 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Max Valentin Staller · 2023 to 2026
$1.5M
NIGMS NIH HHS R35 GM150813
6 · The paper itself

Abstract

Transcription factors activate gene expression in development, homeostasis, and stress with DNA binding domains and activation domains. Although there exist excellent computational models for predicting DNA binding domains from protein sequence, models for predicting activation domains from protein sequence have lagged, particularly in metazoans. We recently developed a simple and accurate predictor of acidic activation domains on human transcription factors. Here, we show how the accuracy of this human predictor arises from the clustering of aromatic, leucine, and acidic residues, which together are necessary for acidic activation domain function. When we combine our predictor with the predictions of convolutional neural network (CNN) models trained in yeast, the intersection is more accurate than individual models, emphasizing that each approach carries orthogonal information. We synthesize these findings into a new set of activation domain predictions on human transcription factors.

Indexed as

DNA-Binding ProteinsTranscription FactorsAmino Acid SequenceDNAHumansSaccharomyces cerevisiaeTranscriptional ActivationDNADNA-Binding ProteinsTranscription Factorsactivation domainconvolutional neural networkprotein function predictiontransactivation domaintranscriptiontranscriptional activation domaintranscription factor

Identifiers

PMID37462277
PMCPMC10550315

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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.