Evidence map›Paper›PMID 28972163›Full record

ArticleThe Journal of biological chemistry2017

An N-terminal di-proline motif is essential for fatty acid-dependent degradation of Δ9-desaturase in

Akira Murakami, Kohjiro Nagao, Naoto Juni, Yuji Hara, Masato Umeda

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

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  13. Organelle aging: Lessons from model organisms.Journal of genetics and genomics = Yi chuan xue bao · 2019
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Akira MurakamiDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510.
Kohjiro NagaoDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510. Electronic address: nagao@sbchem.kyoto-u.ac.jp.
Naoto JuniDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510.
Yuji HaraDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510; AMED-PRIME, Japan Agency for Medical Research and Development, Tokyo 100-0004, Japan.
Masato UmedaDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510. Electronic address: umeda@sbchem.kyoto-u.ac.jp.
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Δ9-fatty acid desaturase introduces a double bond at the Δ9 position of the acyl moiety of acyl-CoA and regulates the cellular levels of unsaturated fatty acids. However, it is unclear how Δ9-desaturase expression is regulated in response to changes in the levels of fatty acid desaturation. In this study, we found that the degradation of DESAT1, the sole Δ9-desaturase in the

Indexed as

ProteolysisAmino Acid MotifsAnimalsDrosophila melanogasterDrosophila ProteinsFatty Acid DesaturasesFatty Acids, UnsaturatedGene Expression Regulation, EnzymologicMiceProlinedesat1 protein, DrosophilaDrosophila ProteinsFatty Acid DesaturasesFatty Acids, UnsaturatedProlineDrosophilafatty acidlipid synthesisphospholipidprotein degradation

Identifiers

PMID28972163
PMCPMC5723986
OpenAlexW2759161762

What OpenQuestion holds

Textmetadata
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.