Evidence map›Paper›PMID 32439656›Full record

ArticleScience (New York, N.Y.)2020

Structural basis for membrane insertion by the human ER membrane protein complex.

Tino Pleiner, Giovani Pinton Tomaleri, Kurt Januszyk, Alison J Inglis, Masami Hazu, Rebecca M Voorhees

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

108 citing papers in PubMed, 177 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
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  9. Review
  10. Review
  11. Review
  12. Article
  13. Structural evolution of the MTCH family of mitochondrial insertases.bioRxiv : the preprint server for biology · 2026
    Article
  14. Article
  15. Article
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  17. Article
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  19. Review
  20. Review

48 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Tino Pleiner *Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Ave., Pasadena, CA 91125, USA.ORCID 0000-0002-5104-0315
Giovani Pinton Tomaleri *Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Ave., Pasadena, CA 91125, USA.ORCID 0000-0001-9661-6480
Kurt Januszyk *Division of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Ave., Pasadena, CA 91125, USA.ORCID 0000-0002-9076-4180
Alison J InglisDivision of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Ave., Pasadena, CA 91125, USA.ORCID 0000-0002-9008-8565
Masami HazuDivision of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Ave., Pasadena, CA 91125, USA.ORCID 0000-0002-6527-9597
Rebecca M VoorheesDivision of Biology and Biological Engineering, California Institute of Technology, 1200 E. California Ave., Pasadena, CA 91125, USA. voorhees@caltech.edu.ORCID 0000-0003-1640-2293
California Institute of Technology · US

Funding

Protein complex assembly in the ER membraneDP2GM137412 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI VOORHEES, REBECCA · 2019 to 2019
$2.5M
NIGMS NIH HHS DP2 GM137412
6 · The paper itself

Abstract

A defining step in the biogenesis of a membrane protein is the insertion of its hydrophobic transmembrane helices into the lipid bilayer. The nine-subunit endoplasmic reticulum (ER) membrane protein complex (EMC) is a conserved co- and posttranslational insertase at the ER. We determined the structure of the human EMC in a lipid nanodisc to an overall resolution of 3.4 angstroms by cryo-electron microscopy, permitting building of a nearly complete atomic model. We used structure-guided mutagenesis to demonstrate that substrate insertion requires a methionine-rich cytosolic loop and occurs via an enclosed hydrophilic vestibule within the membrane formed by the subunits EMC3 and EMC6. We propose that the EMC uses local membrane thinning and a positively charged patch to decrease the energetic barrier for insertion into the bilayer.

Indexed as

Endoplasmic ReticulumHumansIntracellular MembranesLipid BilayersMembrane ProteinsMultiprotein ComplexesEMC6 protein, humanLipid BilayersMembrane ProteinsMultiprotein Complexes

Identifiers

PMID32439656
PMCPMC7547852
OpenAlexW3026613429

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.