Evidence map›Paper›PMID 35742810›Full record

ArticleInternational journal of molecular sciences2022

Structural and Functional Insights into CP2c Transcription Factor Complexes.

Seung Han Son, Min Young Kim, Eunbi Jo, Vladimir N Uversky, Chul Geun Kim

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. SUMOylation-mediated PSME3-20Science advances · 2023
    Article
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

5 authors.

Seung Han SonDepartment of Life Science, Research Institute for Natural Sciences, College of Natural Sciences, Hanyang University, Seoul 04763, Korea.
Min Young KimDepartment of Life Science, Research Institute for Natural Sciences, College of Natural Sciences, Hanyang University, Seoul 04763, Korea.ORCID 0000-0002-7001-3670
Eunbi JoDepartment of Life Science, Research Institute for Natural Sciences, College of Natural Sciences, Hanyang University, Seoul 04763, Korea.
Vladimir N UverskyDepartment of Molecular Medicine, USF Health Byrd Alzheimer's Research Institute, Morsani College of Medicine, University of South Florida, Tampa, FL 33612, USA.ORCID 0000-0002-4037-5857
Chul Geun KimDepartment of Life Science, Research Institute for Natural Sciences, College of Natural Sciences, Hanyang University, Seoul 04763, Korea.ORCID 0000-0002-5848-3338

Funding

National Research Foundation (NRF) of Korea 2010-0025223, NRF-2020R1A2C2009112, NRF-2017M3A9C8027975
6 · The paper itself

Abstract

CP2c, also known as TFCP2, α-CP2, LSF, and LBP-1c, is a prototypic member of the transcription factor (TF) CP2 subfamily involved in diverse ubiquitous and tissue/stage-specific cellular processes and in human malignancies including cancer. Despite its importance, many fundamental regulatory mechanisms of CP2c are still unclear. Here, we uncover unprecedented structural and functional aspects of CP2c using DSP crosslinking and Western blot in addition to conventional methods. We found that a monomeric form of a CP2c homotetramer (tCP2c; [C4]) binds to the known CP2c-binding DNA motif (CNRG-N(5~6)-CNRG), whereas a dimeric form of a CP2c, CP2b, and PIAS1 heterohexamer ([C2B2P2]

Indexed as

DNA-Binding ProteinsTranscription FactorsCell NucleusGene Expression RegulationHumansDNA-Binding ProteinsTFCP2 protein, humanTranscription FactorsDNA binding motifssubcellular localizationtherapeuticstranscriptional regulationtranscription factor CP2c complexes

Identifiers

PMID35742810
PMCPMC9223585

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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.