Evidence map›Paper›PMID 35851188›Full record

ArticleNature structural & molecular biology2022

Structurally derived universal mechanism for the catalytic cycle of the tail-anchored targeting factor Get3.

Michelle Y Fry, Vladimíra Najdrová, Ailiena O Maggiolo, Shyam M Saladi, Pavel Doležal, William M Clemons

Abstract read
PubMed Publisher
In one paragraph

Article in Nature structural & molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Evolutionary remodeling of a remnant GET pathway factor into PEX38, an essential peroxin.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Nucleotide- and metalloid-driven conformational changes in the arsenite efflux ATPase ArsA.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Automated model-free analysis of cryo-EM volume ensembles with SIREn.bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. A unifying model for membrane protein biogenesis.Nature structural & molecular biology · 2024
    Review
  10. Article
  11. Article
  12. Likelihood-based docking of models into cryo-EM maps.Acta crystallographica. Section D, Structural biology · 2023
    Article
  13. Review
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

6 authors at 2 institutions in 2 countries.

Michelle Y FryDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.
Vladimíra NajdrováDepartment of Parasitology, Faculty of Science, BIOCEV, Charles University, Prague, Czech Republic.ORCID http://orcid.org/0000-0002-1971-3882
Ailiena O MaggioloDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.ORCID http://orcid.org/0000-0003-1707-5060
Shyam M SaladiDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.ORCID http://orcid.org/0000-0001-9701-3059
Pavel DoležalDepartment of Parasitology, Faculty of Science, BIOCEV, Charles University, Prague, Czech Republic.ORCID http://orcid.org/0000-0003-1285-9026
William M ClemonsDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA. clemons@caltech.edu.ORCID http://orcid.org/0000-0002-0021-889X
California Institute of Technology · USCharles University · CZ

Funding

Pacific Northwest Center for Cryo-EM - Screening supplementU24GM129547 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI EVANS, JAMES E, GOUAUX, JAMES E · 2018 to 2023
$54.8M
NIH Pioneer AwardDP1GM105385 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CLEMONS, WILLIAM M. · 2012 to 2015
$3.3M
A New Pradigm for the Rational Expression of Integral Membrane ProteinsR01GM125063 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CLEMONS, WILLIAM M., MILLER, THOMAS FRANCIS · 2017 to 2020
$1.5M
Targeting of tail-anchored membrane proteins by the Get pathway.R01GM097572 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CLEMONS, WILLIAM M. · 2011 to 2015
$1.5M
NIGMS NIH HHS DP1 GM105385NIGMS NIH HHS R01 GM097572NIGMS NIH HHS R01 GM125063NIGMS NIH HHS U24 GM129547
6 · The paper itself

Abstract

Tail-anchored (TA) membrane proteins, accounting for roughly 2% of proteomes, are primarily targeted posttranslationally to the endoplasmic reticulum membrane by the guided entry of TA proteins (GET) pathway. For this complicated process, it remains unknown how the central targeting factor Get3 uses nucleotide to facilitate large conformational changes to recognize then bind clients while also preventing exposure of hydrophobic surfaces. Here, we identify the GET pathway in Giardia intestinalis and present the structure of the Get3-client complex in the critical postnucleotide-hydrolysis state, demonstrating that Get3 reorganizes the client-binding domain (CBD) to accommodate and shield the client transmembrane helix. Four additional structures of GiGet3, spanning the nucleotide-free (apo) open to closed transition and the ATP-bound state, reveal the details of nucleotide stabilization and occluded CBD. This work resolves key conundrums and allows for a complete model of the dramatic conformational landscape of Get3.

Indexed as

Saccharomyces cerevisiae ProteinsAdenosine TriphosphatasesGuanine Nucleotide Exchange FactorsHumansProtein TransportSaccharomyces cerevisiaeAdenosine TriphosphatasesGuanine Nucleotide Exchange FactorsSaccharomyces cerevisiae Proteins

Identifiers

PMID35851188
OpenAlexW4285728430

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.