Evidence map›Paper›PMID 32326186›Full record

ArticleInternational journal of molecular sciences2020

Comparison of Target Recognition by TRAF1 and TRAF2.

Chang Min Kim, Hyun Ho Park

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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
0.3field-weighted citation impact, top 50% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Journal of Zhejiang University. Science. B · 2022
    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

2 authors at 1 institution in 1 country.

Chang Min KimCollege of Pharmacy, Chung-Ang University, Dongjag-gu, Seoul 06974, Korea.
Hyun Ho ParkCollege of Pharmacy, Chung-Ang University, Dongjag-gu, Seoul 06974, Korea.ORCID 0000-0001-9928-0847
Chung-Ang University · KR

Funding

National Research Foundation of Korea NRF-2017M3A9D8062960National Research Foundation of Korea NRF-2018R1A2B2003635
6 · The paper itself

Abstract

Although TRAF1 and TRAF2 share common receptors and have extremely conserved amino acid residues, recent studies have shown that key differences in receptor binding preferences with different affinities exist, which might be important for their different functions in TRAF-mediated signal transduction. To better understand TRAF1 and TRAF2 signaling, we analyzed and compared their receptor binding-affinities. Our study revealed that TRADD, TANK, and caspase-2 bind to both TRAF1 and TRAF2 with different affinities in vitro. Sequence and structural analyses revealed that S454 on TRAF2 (corresponding to A369 of TRAF1) is critical for the binding of TRADD, and F347 on TRAF1 (corresponding to L432 of TRAF2) is a critical determinant for high affinity binding of TANK and caspase-2.

Indexed as

Amino Acid SequenceBinding SitesCaspase 2HumansModels, MolecularProtein BindingProtein ConformationProtein Interaction Domains and MotifsStructure-Activity RelationshipTNF Receptor-Associated Factor 1TNF Receptor-Associated Factor 2Caspase 2TNF Receptor-Associated Factor 1TNF Receptor-Associated Factor 2apoptosisinflammationprotein interactionTRADDTRAF

Identifiers

PMID32326186
PMCPMC7215387
OpenAlexW3018698140

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.