Evidence map›Paper›PMID 26399276›Full record

ReviewSmall GTPases2015

Novel topography of the Rab11-effector interaction network within a ciliary membrane targeting complex.

Melanie Vetter, Jing Wang, Esben Lorentzen, Dusanka Deretic

Open access · bronzeAbstract readReview
In one paragraph

Review in Small GTPases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Host Cell Signatures of the Envelopment Site within Beta-Herpes Virions.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. New Insights into How Trafficking Regulates T Cell Receptor Signaling.Frontiers in cell and developmental biology · 2016
    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

4 authors at 2 institutions in 3 countries.

Melanie Vettera Department of Structural Cell Biology ; Max-Planck-Institute of Biochemistry ; Martinsried , Germany.
Jing Wangb Departments of Surgery ; Division of Ophthalmology; University of New Mexico ; Albuquerque , NM USA.
Esben Lorentzena Department of Structural Cell Biology ; Max-Planck-Institute of Biochemistry ; Martinsried , Germany.
Dusanka Dereticb Departments of Surgery ; Division of Ophthalmology; University of New Mexico ; Albuquerque , NM USA.
Max Planck Institute of Biochemistry · DEOphthalmology Associates (United States) · US

Funding

Rhodopsin Trafficking & Photoreceptor Membrane RenewalR01EY012421 · NEI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI DERETIC, DUSANKA DANIELLE · 1999 to 2023
$7.2M
European Research Council 310343NEI NIH HHS R01 EY012421
6 · The paper itself

Abstract

Small GTPases function as universal molecular switches due to the nucleotide dependent conformational changes of their switch regions that allow interacting proteins to discriminate between the active GTP-bound and the inactive GDP-bound states. Guanine nucleotide exchange factors (GEFs) recognize the inactive GDP-bound conformation whereas GTPase activating proteins (GAPs), and the GTPase effectors recognize the active GTP-bound state. Small GTPases are linked to each other through regulatory and effector proteins into functional networks that regulate intracellular membrane traffic through diverse mechanisms that include GEF and GAP cascades, GEF-effector interactions, common effectors and positive feedback loops linking interacting proteins. As more structural and functional information is becoming available, new types of interactions between regulatory proteins, and new mechanisms by which GTPases are networked to control membrane traffic are being revealed. This review will focus on the structure and function of the novel Rab11-FIP3-Rabin8 dual effector complex and its implications for the targeting of sensory receptors to primary cilia, dysfunction of which causes cilia defects underlying human diseases and disorders know as ciliopathies.

Indexed as

Signal TransductionAnimalsCell MembraneCiliaCiliopathiesGerminal Center KinasesHumansI-kappa B KinaseMultienzyme ComplexesProtein Serine-Threonine Kinasesrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsGerminal Center KinasesI-kappa B KinaseIKBKG protein, humanMultienzyme ComplexesProtein Serine-Threonine Kinasesrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsciliumGolgiGTPase effectorsmembrane traffickingRab GTPases

Identifiers

PMID26399276
PMCPMC4905263
OpenAlexW2281917463

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.