Evidence map›Paper›PMID 15877277›Full record

ReviewAmerican journal of human genetics2005

Single-gene disorders: what role could moonlighting enzymes play?

Ganesh Sriram, Julian A Martinez, Edward R B McCabe, James C Liao, Katrina M Dipple

Open access · bronzeAbstract readReview
In one paragraph

Review in American journal of human genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

85 citing papers in PubMed, 218 citations in OpenAlex.

  1. Trial
  2. The XRE family protein DbuR is a transcriptional repressor of theApplied and environmental microbiology · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Moonlighting enzymes: when cellular context defines specificity.Cellular and molecular life sciences : CMLS · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Isolated Mitochondrial Preparations andCurrent neuropharmacology · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Moonlighting Proteins: The Case of the Hexokinases.Frontiers in molecular biosciences · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Multiple Forms of Multifunctional Proteins in Health and Disease.Frontiers in cell and developmental biology · 2020
    Review
  19. Review
  20. Article

25 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 2 countries.

Ganesh SriramDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-7088, USA.
Julian A Martinez
Edward R B McCabe
James C Liao
Katrina M Dipple
University of California, Los Angeles · USMattel Children's Hospital · USMedical Genetics Center · DESamueli Institute · US

Funding

MOLECULAR GENETIC STUDIES OF GLYCEROL KINASE DEFICIENCYR01HD022563 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCCABE, EDWARD R · 1987 to 2003
$1.1M
Glycerol Kinase Deficiency to Study Metabolic DiseasesR01GM067929 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DIPPLE, KATRINA M · 2003 to 2005
$873k
Molecular Mechanisms of Glycerol Kinase DeficiencyK08DK060055 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DIPPLE, KATRINA M · 2001 to 2005
$605k
NICHD NIH HHS R01 HD022563NICHD NIH HHS R01 HD22563NIDDK NIH HHS K08 DK060055NIDDK NIH HHS K08 DK60055NIGMS NIH HHS R01 GM067929
6 · The paper itself

Abstract

Single-gene disorders with "simple" Mendelian inheritance do not always imply that there will be an easy prediction of the phenotype from the genotype, which has been shown for a number of metabolic disorders. We propose that moonlighting enzymes (i.e., metabolic enzymes with additional functional activities) could contribute to the complexity of such disorders. The lack of knowledge about the additional functional activities of proteins could result in a lack of correlation between genotype and phenotype. In this review, we highlight some notable and recent examples of moonlighting enzymes and their possible contributions to human disease. Because knowledge and cataloging of the moonlighting activities of proteins are essential for the study of cellular function and human physiology, we also review recently reported and recommended methods for the discovery of moonlighting activities.

Indexed as

AnimalsApoptosisGene Expression RegulationGenetic Diseases, InbornHumansMolecular BiologyMultienzyme ComplexesProteinsSignal TransductionStructure-Activity RelationshipTranscription, GeneticMultienzyme ComplexesProteins

Identifiers

PMID15877277
PMCPMC1196451
OpenAlexW2030141485

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.