Evidence map›Paper›PMID 30928671›Full record

ReviewCurrent opinion in cell biology2019

Trafficking mechanisms of P-type ATPase copper transporters.

Cortnie Hartwig, Stephanie A Zlatic, Melissa Wallin, Alysia Vrailas-Mortimer, Christoph J Fahrni, Victor Faundez

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Review
  6. Review
  7. Current Management of Neurological Wilson's Disease.Tremor and other hyperkinetic movements (New York, N.Y.) · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Copper in Gynecological Diseases.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  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

6 authors at 4 institutions in 1 country.

Cortnie HartwigDepartment of Cell Biology, Emory University, Atlanta, GA 30322, United States.
Stephanie A ZlaticDepartment of Cell Biology, Emory University, Atlanta, GA 30322, United States.
Melissa WallinMedical Illustration Graduate Program, Augusta University, Augusta, GA 30912, United States.
Alysia Vrailas-MortimerSchool of Biological Sciences, Illinois State University, Normal 61790, United States.
Christoph J FahrniSchool of Chemistry and Biochemistry and Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, United States.
Victor FaundezDepartment of Cell Biology, Emory University, Atlanta, GA 30322, United States. Electronic address: vfaunde@emory.edu.
Emory University · USAugusta University · USGeorgia Institute of Technology · USIllinois State University · US

Funding

IRACDA Fellowships in Research and Science Training (FIRST)K12GM000680 · NIGMS · EMORY UNIVERSITY · PI BROWN, LOU ANN S, MCCARTY, NAEL A · 2000 to 2024
$41.2M
Molecular Tools to Illuminate Copper Transport and HomeostasisR01GM067169 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI FAHRNI, CHRISTOPH J · 2004 to 2018
$3.5M
Neuronal Mechanisms of Copper Transport and ToxicityRF1AG060285 · NIA · EMORY UNIVERSITY · PI FAUNDEZ, VICTOR · 2018 to 2021
$2.4M
The Role of p38K and protein homeostasis in Limb-Girdle Muscular DystrophiesR15AR070505 · NIAMS · ILLINOIS STATE UNIVERSITY · PI VRAILAS-MORTIMER, ALYSIA DANIELLE · 2016 to 2016
$435k
NIAMS NIH HHS R15 AR070505NIA NIH HHS RF1 AG060285NIGMS NIH HHS K12 GM000680NIGMS NIH HHS R01 GM067169
6 · The paper itself

Abstract

Copper is an essential micronutrient required for oxygen-dependent enzymes, yet excess of the metal is a toxicant. The tug-of-war between these copper activities is balanced by chaperones and membrane transporters, which control copper distribution and availability. The P-type ATPase transporters, ATP7A and ATP7B, regulate cytoplasmic copper by pumping copper out of cells or into the endomembrane system. Mutations in ATP7A and ATP7B cause diseases that share neuropsychiatric phenotypes, which are similar to phenotypes observed in mutations affecting cytoplasmic trafficking complexes required for ATP7A/B dynamics. Here, we discuss evidence indicating that phenotypes associated to genetic defects in trafficking complexes, such as retromer and the adaptor complex AP-1, result in part from copper dyshomeostasis due to mislocalized ATP7A and ATP7B.

Indexed as

AnimalsCopper-Transporting ATPasesCopper Transport ProteinsHumansMitochondriaMutationParkinson DiseaseProtein TransportCopper-Transporting ATPasesCopper Transport Proteins

Identifiers

PMID30928671
PMCPMC6726579
OpenAlexW2928439698

What OpenQuestion holds

Textmetadata
LicenceTDM
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.