Evidence map›Paper›PMID 30647138›Full record

ReviewBiochemical Society transactions2019

Structure and mechanism of the ESCRT pathway AAA+ ATPase Vps4.

Han Han, Christopher P Hill

Abstract readReview
In one paragraph

Review in Biochemical Society transactions, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. The role of Vps4 in cancer development.Frontiers in oncology · 2023
    Review
  11. Friction-driven membrane scission by the human ESCRT-III proteins CHMP1B and IST1.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
  13. Article
  14. Deliver on Time or Pay the Fine: Scheduling in Membrane Trafficking.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Mitochondrial Surveillance by Cdc48/p97: MAD vs. Membrane Fusion.International journal of molecular sciences · 2020
    Review
  19. Mechanisms of eukaryotic replisome disassembly.Biochemical Society transactions · 2020
    Review
  20. 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.

Han HanDepartment of Biochemistry, University of Utah, Salt Lake City, UT 84112-5650, U.S.A.
Christopher P HillDepartment of Biochemistry, University of Utah, Salt Lake City, UT 84112-5650, U.S.A. chris@biochem.utah.edu.ORCID 0000-0001-6796-7740

Funding

X-ray Cryst. CoreP50GM082545 · NIGMS · UNIVERSITY OF UTAH · PI SUNDQUIST, WESLEY I. · 2007 to 2018
$51.1M
6 · The paper itself

Abstract

The progression of ESCRT (Endosomal Sorting Complexes Required for Transport) pathways, which mediate numerous cellular membrane fission events, is driven by the enzyme Vps4. Understanding of Vps4 mechanism is, therefore, of fundamental importance in its own right and, moreover, it is highly relevant to the understanding of many related AAA+ ATPases that function in multiple facets of cell biology. Vps4 unfolds its ESCRT-III protein substrates by translocating them through its central hexameric pore, thereby driving membrane fission and recycling of ESCRT-III subunits. This mini-review focuses on recent advances in Vps4 structure and mechanism, including ideas about how Vps4 translocates and unfolds ESCRT-III subunits. Related AAA+ ATPases that share structural features with Vps4 and likely utilize an equivalent mechanism are also discussed.

Indexed as

AnimalsATPases Associated with Diverse Cellular ActivitiesCryoelectron MicroscopyEndosomal Sorting Complexes Required for TransportEndosomesHumansProtein SubunitsVacuolar Proton-Translocating ATPasesATPases Associated with Diverse Cellular ActivitiesEndosomal Sorting Complexes Required for TransportProtein SubunitsVacuolar Proton-Translocating ATPasesVPS4A protein, humanAAA proteinscryo-electron microscopyendosomal sortingprotein disassemblyprotein structure

Identifiers

PMID30647138
PMCPMC6393862

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.