Evidence map›Paper›PMID 21359175›Full record

ArticlePloS one2011

Identification of the PDI-family member ERp90 as an interaction partner of ERFAD.

Jan Riemer, Henning G Hansen, Christian Appenzeller-Herzog, Linda Johansson, Lars Ellgaard

Abstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. How Are Proteins Reduced in the Endoplasmic Reticulum?Trends in biochemical sciences · 2018
    Review
  9. Article
  10. Review
  11. N-linked sugar-regulated protein folding and quality control in the ER.Seminars in cell & developmental biology · 2015
    Review
  12. Article
  13. The mammalian endoplasmic reticulum-associated degradation system.Cold Spring Harbor perspectives in biology · 2013
    Review
  14. Article
  15. Article
  16. Article
  17. 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.

Jan RiemerDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Henning G Hansen
Christian Appenzeller-Herzog
Linda Johansson
Lars Ellgaard

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the endoplasmic reticulum (ER), members of the protein disulfide isomerase (PDI) family perform critical functions during protein maturation. Herein, we identify the previously uncharacterized PDI-family member ERp90. In cultured human cells, we find ERp90 to be a soluble ER-luminal glycoprotein that comprises five potential thioredoxin (Trx)-like domains. Mature ERp90 contains 10 cysteine residues, of which at least some form intramolecular disulfides. While none of the Trx domains contain a canonical Cys-Xaa-Xaa-Cys active-site motif, other conserved cysteines could endow the protein with redox activity. Importantly, we show that ERp90 co-immunoprecipitates with ERFAD, a flavoprotein involved in ER-associated degradation (ERAD), through what is most likely a direct interaction. We propose that the function of ERp90 is related to substrate recruitment or delivery to the ERAD retrotranslocation machinery by ERFAD.

Indexed as

Amino Acid SequenceAntigens, NeoplasmCarbohydrate SequenceCells, CulturedEndoplasmic ReticulumFlavoproteinsGlycoproteinsGreen Fluorescent ProteinsHumansImmunoprecipitationMembrane GlycoproteinsMolecular Sequence DataMultigene FamilyPolysaccharidesProtein BindingProtein Disulfide-IsomerasesAntigens, NeoplasmFlavoproteinsFOXRED2 protein, humanGlycoproteinsGreen Fluorescent ProteinsMembrane GlycoproteinsPolysaccharidesProtein Disulfide-IsomerasesRecombinant ProteinsTXNDC16 protein, human

Identifiers

PMID21359175
PMCPMC3040216

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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.