Evidence map›Paper›PMID 40996706›Full record

ArticleDatabase : the journal of biological databases and curation2025

p53motifDB: integration of genomic information and tumour suppressor p53 binding motifs.

Gabriele Baniulyte, Sawyer M Hicks, Morgan A Sammons

Abstract read
In one paragraph

Article in Database : the journal of biological databases and curation, 2025. 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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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

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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

The trial behind it

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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

5 · Who and what money

Authors and funding

3 authors.

Gabriele BaniulyteDepartment of Biological Sciences and the RNA Institute, University at Albany, SUNY, 1400 Washington Ave, Life Sciences Building Room 2078, Albany, NY 12222, United States.
Sawyer M HicksDepartment of Biological Sciences and the RNA Institute, University at Albany, SUNY, 1400 Washington Ave, Life Sciences Building Room 2078, Albany, NY 12222, United States.
Morgan A SammonsDepartment of Biological Sciences and the RNA Institute, University at Albany, SUNY, 1400 Washington Ave, Life Sciences Building Room 2078, Albany, NY 12222, United States.ORCID 0000-0002-5329-1169

Funding

Defining cis-regulatory networks controlling a core stress responseR35GM138120 · NIGMS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI SAMMONS, MORGAN ANDREW · 2020 to 2024
$1.8M
NIGMS NIH HHS R35 GM138120NIH HHS GM138120
6 · The paper itself

Abstract

The tumour suppressor gene TP53 encodes the DNA binding transcription factor p53 and is one of the most mutated genes in human cancer. Tumour suppressor activity requires binding of p53 to its DNA response elements and subsequent transcriptional activation of a diverse set of target genes. Despite decades of close study, the logic underlying p53 interactions with its numerous potential genomic binding sites and target genes is not yet fully understood. Here, we present a database of DNA and chromatin-based information focused on putative p53 binding sites in the human genome to allow users to generate and test new hypotheses related to p53 activity in the genome. Users can query genomic locations based on experimentally observed p53 binding, regulatory element activity, genetic variation, evolutionary conservation, chromatin modification state, and chromatin structure. We present multiple use cases demonstrating the utility of this database for generating novel biological hypotheses, such as chromatin-based determinants of p53 binding and potential cell type-specific p53 activity. All database information is also available as a precompiled SQLite database for use in local analysis or as a Shiny web application. Database URL: https://p53motifDB.its.albany.edu.

Indexed as

Databases, GeneticGenome, HumanGenomicsTumor Suppressor Protein p53Binding SitesChromatinHumansNucleotide MotifsChromatinTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID40996706
PMCPMC12462388

What OpenQuestion holds

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LicenceCC BY
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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.