Evidence map›Paper›PMID 35977012›Full record

ArticleScience advances2022

A synthetic biology approach reveals diverse and dynamic CDK response profiles via multisite phosphorylation of NLS-NES modules.

Ilona Faustova, Mihkel Örd, Viacheslav Kiselev, Dmytro Fedorenko, Irina Borovko, Dags Macs, Kaur Pääbo, Marko Lõoke, Mart Loog

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 24% of its field
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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Decoding Cdk1 control: from mitotic thresholds to meiotic specificity.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
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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

9 authors at 1 institution in 1 country.

Ilona FaustovaInstitute of Technology, University of Tartu, Tartu 50411, Estonia.ORCID 0000-0002-6327-5293
Mihkel ÖrdInstitute of Technology, University of Tartu, Tartu 50411, Estonia.ORCID 0000-0003-0454-7241
Viacheslav KiselevInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Dmytro FedorenkoInstitute of Technology, University of Tartu, Tartu 50411, Estonia.ORCID 0000-0001-7883-7001
Irina BorovkoInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Dags MacsInstitute of Technology, University of Tartu, Tartu 50411, Estonia.ORCID 0000-0002-9644-3601
Kaur PääboInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Marko LõokeInstitute of Technology, University of Tartu, Tartu 50411, Estonia.
Mart LoogInstitute of Technology, University of Tartu, Tartu 50411, Estonia.ORCID 0000-0003-1330-8453
University of Tartu · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complexity of multisite phosphorylation mechanisms in regulating nuclear localization signals (NLSs) and nuclear export signals (NESs) is not understood, and its potential has not been used in synthetic biology. The nucleocytoplasmic shuttling of many proteins is regulated by cyclin-dependent kinases (CDKs) that rely on multisite phosphorylation patterns and short linear motifs (SLiMs) to dynamically control proteins in the cell cycle. We studied the role of motif patterns in nucleocytoplasmic shuttling using sensors based on the CDK targets Dna2, Psy4, and Mcm2/3 of

Identifiers

PMID35977012
PMCPMC9385143
OpenAlexW4292116804

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.