Evidence map›Paper›PMID 28179369›Full record

ArticleThe EMBO journal2017

Nmd3 is a structural mimic of eIF5A, and activates the cpGTPase Lsg1 during 60S ribosome biogenesis.

Andrey G Malyutin, Sharmishtha Musalgaonkar, Stephanie Patchett, Joachim Frank, Arlen W Johnson

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 75 citations in OpenAlex.

  1. RiboScreenBiomedicines · 2026
    Review
  2. Article
  3. Structure of a Gcn2 dimer in complex with the large 60S ribosomal subunit.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  20. Mechanisms and regulation of protein synthesis in mitochondria.Nature reviews. Molecular cell biology · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Andrey G MalyutinDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA.
Sharmishtha MusalgaonkarDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.
Stephanie PatchettDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.
Joachim FrankDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA jf2192@cumc.columbia.edu arlen@mail.utexas.edu.ORCID 0000-0001-5449-6943
Arlen W JohnsonDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA jf2192@cumc.columbia.edu arlen@mail.utexas.edu.ORCID 0000-0002-4742-085X
The University of Texas at Austin · USColumbia University · USHoward Hughes Medical Institute · US

Funding

STRUCTURE ANALYSIS OF MACROMOLECULAR ASSEMBLIESR01GM029169 · NIGMS · WADSWORTH CENTER · PI FRANK, JOACHIM · 1985 to 2019
$6.1M
MRNA DEGRADATION AND TRANSLATION CONTROL IN YEASTR01GM053655 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI JOHNSON, ARLEN W · 1995 to 2017
$5.1M
STRUCTURAL ANALYSIS OF MACROMOLECULAR ASSEMBLYR37GM029169 · NIGMS · WADSWORTH CENTER · PI FRANK, JOACHIM · 1997 to 2006
$2.8M
300 kV Electron Microscope for Structural BiologyS10RR017291 · NCRR · NEW YORK STRUCTURAL BIOLOGY CENTER · PI STOKES, DAVID L · 2002 to 2002
$2.0M
RES FACIL CONSTRUCTION: HALLUCINOGENSC06RR017528 · NCRR · NEW YORK STRUCTURAL BIOLOGY CENTER · PI COWBURN, DAVID · 2002 to 2002
$2.0M
Dual-Beam Scanning Electron Microscope for New York Structural Biology CenterS10RR029300 · NCRR · NEW YORK STRUCTURAL BIOLOGY CENTER · PI STOKES, DAVID L. · 2010 to 2010
$2.0M
Acquisition of Detector for JEOL 3200 FSC Electron MicroscopeS10OD019994 · OD · NEW YORK STRUCTURAL BIOLOGY CENTER · PI CARRAGHER, BRIDGET OLIVIA · 2015 to 2015
$600k
Howard Hughes Medical InstituteNCRR NIH HHS C06 RR017528NCRR NIH HHS S10 RR017291NCRR NIH HHS S10 RR029300NIGMS NIH HHS R01 GM029169NIGMS NIH HHS R01 GM053655NIGMS NIH HHS R37 GM029169NIH HHS S10 OD019994
6 · The paper itself

Abstract

During ribosome biogenesis in eukaryotes, nascent subunits are exported to the cytoplasm in a functionally inactive state. 60S subunits are activated through a series of cytoplasmic maturation events. The last known events in the cytoplasm are the release of Tif6 by Efl1 and Sdo1 and the release of the export adapter, Nmd3, by the GTPase Lsg1. Here, we have used cryo-electron microscopy to determine the structure of the 60S subunit bound by Nmd3, Lsg1, and Tif6. We find that a central domain of Nmd3 mimics the translation elongation factor eIF5A, inserting into the E site of the ribosome and pulling the L1 stalk into a closed position. Additional domains occupy the P site and extend toward the sarcin-ricin loop to interact with Tif6. Nmd3 and Lsg1 together embrace helix 69 of the B2a intersubunit bridge, inducing base flipping that we suggest may activate the GTPase activity of Lsg1.

Indexed as

Organelle BiogenesisCryoelectron MicroscopyGTP-Binding ProteinsRibosomal ProteinsRibosome Subunits, Large, EukaryoticRNA-Binding ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsGTP-Binding ProteinsLSG1 protein, S cerevisiaeNMD3 protein, S cerevisiaeRibosomal ProteinsRNA-Binding ProteinsSaccharomyces cerevisiae ProteinsTIF6 protein, S cerevisiaeeIF5ALSG1NMD3ribosome biogenesis

Identifiers

PMID28179369
PMCPMC5376978
OpenAlexW2586745337

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.