Evidence map›Paper›PMID 29033250›Full record

ReviewMolecular genetics and metabolism2017

Propionyl-CoA carboxylase - A review.

Parith Wongkittichote, Nicholas Ah Mew, Kimberly A Chapman

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular genetics and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 2 pooled it
10.3field-weighted citation impact, top 1% 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

131 citing papers in PubMed, 2 syntheses or guidelines pooled it, 243 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. A circulating odd-chain fatty acid biomarker signature discriminates pediatric allergic rhinitis with asthma from related allergic airway phenotypes.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Article
  8. Article
  9. Adaptation of White Adipocytes to Cooler Temperatures: Impacts on Energy Metabolism and Protein Acetylation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  10. Observational
  11. Article
  12. Article
  13. Article
  14. Propionic acidemia in Mexico: Clinical and genotypic spectrum.Molecular genetics and metabolism reports · 2026
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Age-Associated Metabolomic Changes in Human Spermatozoa.International journal of molecular sciences · 2026
    Article
  20. Article

71 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

3 authors at 1 institution in 1 country.

Parith WongkittichoteChildren's National Health System, Division of Genetics and Metabolism, United States.
Nicholas Ah MewChildren's National Health System, Division of Genetics and Metabolism, United States; Rare Diseases Institute, Division of Genetics and Metabolism, United States.
Kimberly A ChapmanChildren's National Health System, Division of Genetics and Metabolism, United States; Rare Diseases Institute, Division of Genetics and Metabolism, United States. Electronic address: KChapman@childrensnational.org.
Children's National · US

Funding

Lost anaplerosis in Propionic acidemia and Methylmalonic aciduria?K08DK105233 · NIDDK · CHILDREN'S RESEARCH INSTITUTE · PI CHAPMAN, KIMBERLY ANN · 2015 to 2017
$441k
NIDDK NIH HHS K08 DK105233
6 · The paper itself

Abstract

Propionyl-CoA carboxylase (PCC) is the enzyme which catalyzes the carboxylation of propionyl-CoA to methylmalonyl-CoA and is encoded by the genes PCCA and PCCB to form a hetero-dodecamer. Dysfunction of PCC leads to the inherited metabolic disorder propionic acidemia, which can result in an affected individual presenting with metabolic acidosis, hyperammonemia, lethargy, vomiting and sometimes coma and death if not treated. Individuals with propionic acidemia also have a number of long term complications resulting from the dysfunction of the PCC enzyme. Here we present an overview of the current knowledge about the structure and function of PCC. We review an updated list of human variants which are published and provide an overview of the disease.

Indexed as

Carbon-Carbon LigasesHumansHyperammonemiaLactic AcidMethylmalonyl-CoA DecarboxylaseMutationPropionic AcidemiaStructure-Activity RelationshipCarbon-Carbon Ligaseshydracrylic acidLactic AcidMethylmalonyl-CoA Decarboxylasepropionyl CoA carboxylase (ATP-hydrolyzing)3-hydroxypropionateMethylcitratePropionic acidemiaPropionyl-CoA carboxylase

Identifiers

PMID29033250
PMCPMC5725275
OpenAlexW2762198627

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.