Evidence map›Paper›PMID 33202241›Full record

ArticleCurrent biology : CB2020

Cell Biology: Deciphering the ABCs of SLiMs in G1-CDK Signaling.

Jagoree Roy, Martha S Cyert

Open access · bronzeAbstract readComment
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 87% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Jagoree RoyDepartment of Biology, Stanford University, Stanford, CA, USA.
Martha S CyertDepartment of Biology, Stanford University, Stanford, CA, USA. Electronic address: mcyert@stanford.edu.
Stanford University · US

Funding

Systematic elucidation of calcineurin phosphatase signaling in humansR35GM136243 · NIGMS · STANFORD UNIVERSITY · PI Martha S. Cyert · 2020 to 2026
$3.9M
NIGMS NIH HHS R35 GM136243
6 · The paper itself

Abstract

A new study uses an elegant in vivo assay to comprehensively characterize the LP docking motif, which determines G1-CDK substrate specificity in fungi. The authors show that LP-cyclin docking strength determines the timing of Sic1 degradation, a key cell cycle event.

Indexed as

CyclinsSaccharomyces cerevisiae ProteinsPhosphorylationSaccharomyces cerevisiaeSignal TransductionCyclinsSaccharomyces cerevisiae Proteins

Identifiers

PMID33202241
PMCPMC10763628
OpenAlexW3101014408

What OpenQuestion holds

Textmetadata
LicenceTDM
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.