Evidence map›Paper›PMID 29089387›Full record

ArticleThe Journal of biological chemistry2017

Fic-mediated deAMPylation is not dependent on homodimerization and rescues toxic AMPylation in flies.

Amanda K Casey, Andrew T Moehlman, Junmei Zhang, Kelly A Servage, Helmut Krämer, Kim Orth

Erratum issuedAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. Inhibition of FicD-mediated AMPylation and deAMPylation by isoprenoid diphosphates.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Ribonuclease RNase Z is an evolutionarily conserved deAMPylase.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. FicD sensitizes cellular response to glucose fluctuations in mouse embryonic fibroblasts.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. AMPylation and Endoplasmic Reticulum Protein Folding Homeostasis.Cold Spring Harbor perspectives in biology · 2023
    Review
  17. The Alarmone Diadenosine Tetraphosphate as a Cosubstrate for Protein AMPylation.Angewandte Chemie (International ed. in English) · 2023
    Article
  18. Article
  19. Fic-mediated AMPylation tempers the unfolded protein response during physiological stress.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. Production of an Active, Human Membrane Protein inInternational journal of molecular sciences · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Amanda K CaseyFrom the Department of Molecular Biology.ORCID 0000-0002-5829-748X
Andrew T Moehlmanthe Department of Neuroscience.
Junmei ZhangFrom the Department of Molecular Biology.
Kelly A ServageFrom the Department of Molecular Biology.
Helmut Krämerthe Department of Neuroscience.ORCID 0000-0002-1167-2676
Kim OrthFrom the Department of Molecular Biology, Kim.Orth@UTSouthwestern.edu.ORCID 0000-0002-0678-7620

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
MOLECULAR ANALYSIS OF THE BOSS TRANSMEMBRANE LIGANDR01EY010199 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI Helmut J Kramer · 1994 to 2026
$9.7M
AMPylation, a novel mechanism regulating visual neurotransmissionR01EY021922 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI KRAMER, HELMUT J · 2011 to 2015
$1.7M
Proteostasis, AMPylation and the Unfolded Protein repsonse (UPR)R01GM115188 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ORTH, KIM · 2015 to 2018
$1.2M
SEM for UT Southwestern EM Core FacilityS10OD020103 · OD · UT SOUTHWESTERN MEDICAL CENTER · PI LUBY-PHELPS, KATHERINE J · 2015 to 2015
$306k
NEI NIH HHS R01 EY010199NEI NIH HHS R01 EY021922NIGMS NIH HHS R01 GM115188NIH HHS P40 OD018537NIH HHS S10 OD020103
6 · The paper itself

Abstract

Protein chaperones play a critical role in proteostasis. The activity of the major endoplasmic reticulum chaperone BiP (GRP78) is regulated by Fic-mediated AMPylation during resting states. By contrast, during times of stress, BiP is deAMPylated. Here, we show that excessive AMPylation by a constitutively active Fic

Indexed as

Protein Processing, Post-TranslationalAdenosine MonophosphateAmino Acid SubstitutionAnimalsAnimals, Genetically ModifiedCell LineCRISPR-Cas SystemsDimerizationDrosophila melanogasterDrosophila ProteinsEndoplasmic Reticulum Chaperone BiPEndoplasmic Reticulum StressEye AbnormalitiesFemaleHeat-Shock ProteinsHomozygoteAdenosine MonophosphateDrosophila ProteinsEndoplasmic Reticulum Chaperone BiPFic protein, DrosophilaHeat-Shock ProteinsNucleotidyltransferasesRecombinant ProteinsAMPylationBiPdeAMPylationdimerizationDrosophilaendoplasmic reticulum stress (ER stress)FicGRP78unfolded protein response (UPR)

Identifiers

PMID29089387
PMCPMC5743091

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.