Evidence map›Paper›PMID 24981771›Full record

ReviewChemistry & biology2014

Genetic, structural, and molecular insights into the function of ras of complex proteins domains.

Laura Civiero, Sybille Dihanich, Patrick A Lewis, Elisa Greggio

Open access · hybridAbstract readReview
In one paragraph

Review in Chemistry & biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Leucine-rich repeat kinase 2 at a glance.Journal of cell science · 2023
    Article
  3. Exploring the focal role of LRRK2 kinase in Parkinson's disease.Environmental science and pollution research international · 2022
    Review
  4. Article
  5. Article
  6. The dynamic switch mechanism that leads to activation of LRRK2 is embedded in the DFGψ motif in the kinase domain.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  7. Review
  8. The LRRK2 signalling system.Cell and tissue research · 2018
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. 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

4 authors at 3 institutions in 2 countries.

Laura CivieroDepartment of Biology, University of Padova, Via U. Bassi 58/b, Padova 35131, Italy.
Sybille DihanichDepartment of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Patrick A LewisDepartment of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK; School of Pharmacy, University of Reading, Whiteknights, Reading RG6 6AP, UK; Centre for Integrated Neuroscience and Neurodynamics, University of Reading, Whiteknights, Reading RG6 6AP, UK. Electronic address: p.a.lewis@reading.ac.uk.
Elisa GreggioDepartment of Biology, University of Padova, Via U. Bassi 58/b, Padova 35131, Italy. Electronic address: elisa.greggio@unipd.it.
University of Padua · ITNational Hospital for Neurology and Neurosurgery · GBUniversity of Reading · GB

Funding

Medical Research Council MC_G1000735Medical Research Council MR/L010933/1Parkinson's UK F-1002Telethon GGP12237Wellcome Trust 089698
6 · The paper itself

Abstract

Ras of complex proteins (ROC) domains were identified in 2003 as GTP binding modules in large multidomain proteins from Dictyostelium discoideum. Research into the function of these domains exploded with their identification in a number of proteins linked to human disease, including leucine-rich repeat kinase 2 (LRRK2) and death-associated protein kinase 1 (DAPK1) in Parkinson's disease and cancer, respectively. This surge in research has resulted in a growing body of data revealing the role that ROC domains play in regulating protein function and signaling pathways. In this review, recent advances in the structural information available for proteins containing ROC domains, along with insights into enzymatic function and the integration of ROC domains as molecular switches in a cellular and organismal context, are explored.

Indexed as

Protein Structure, TertiaryAnimalsConserved SequenceEvolution, MolecularHumansMolecular Targeted TherapyProteinsProteins

Identifiers

PMID24981771
PMCPMC4104024
OpenAlexW1968867172

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.