Evidence map›Paper›PMID 29408362›Full record

ReviewArchives of biochemistry and biophysics2018

Biosynthesis of human myeloperoxidase.

William M Nauseef

Open access · greenAbstract readReview
In one paragraph

Review in Archives of biochemistry and biophysics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. The Azalea Hypothesis of Alzheimer Disease: A Functional Iron Deficiency Promotes Neurodegeneration.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2024
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Myeloperoxidase Controls Bone Turnover by Suppressing Osteoclast Differentiation Through Modulating Reactive Oxygen Species Level.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  11. Review
  12. Inhibition of Myeloperoxidase.Handbook of experimental pharmacology · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Antimicrobial actions of dual oxidases and lactoperoxidase.Journal of microbiology (Seoul, Korea) · 2018
    Review
  18. Article
  19. Review
  20. Role of inflammatory cells in airway remodeling in COPD.International journal of chronic obstructive pulmonary disease
    Review
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

1 author at 1 institution in 1 country.

William M NauseefInflammation Program and Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine University of Iowa, Veterans Administration Medical Center, Iowa City, IA 52240, USA; Veterans Administration Medical Center, Iowa City, IA 52240, USA; 2501 Crosspark Road D168- MTF, Coralville, IA 52241, USA. Electronic address: william-nauseef@uiowa.edu.
United States Department of Veterans Affairs · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI PATRICK T O'SHAUGHNESSY · 1990 to 2026
$40.5M
Determinants of human neutrophil fate after phagocytosisR01AI132335 · NIAID · UNIVERSITY OF IOWA · PI NAUSEEF, WILLIAM M. · 2018 to 2022
$2.4M
Consequences of interactions between human neutrophils and Staphylococcus aureusR01AI116546 · NIAID · UNIVERSITY OF IOWA · PI NAUSEEF, WILLIAM M. · 2015 to 2019
$1.8M
Human neutrophils, phospholipase A2 and S.aureus: microbial targets and responsesI01BX000513 · VA · IOWA CITY VA MEDICAL CENTER · PI NAUSEEF, WILLIAM M. · 2009 to 2017
–
BLRD VA I01 BX000513NIAID NIH HHS R01 AI116546NIAID NIH HHS R01 AI132335NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Members of Chordata peroxidase subfamily [1] expressed in mammals, including myeloperoxidase (MPO), eosinophil peroxidase (EPO), lactoperoxidase (LPO), and thyroid peroxidase (TPO), express conserved motifs around the heme prosthetic group essential for their activity, a calcium-binding site, and at least two covalent bonds linking the heme group to the protein backbone. Although most studies of the biosynthesis of these peroxidases have focused on MPO, many of the features described occur during biosynthesis of other members of the protein subfamily. Whereas MPO biosynthesis includes events typical for proteins generated in the secretory pathway, the importance and consequences of heme insertion are events uniquely associated with peroxidases. This Review summarizes decades of work elucidating specific steps in the biosynthetic pathway of human MPO. Discussion includes cotranslational glycosylation and subsequent modifications of the N-linked carbohydrate sidechains, contributions by molecular chaperones in the endoplasmic reticulum, cleavage of the propeptide from proMPO, and proteolytic processing of protomers and dimerization to yield mature MPO. Parallels between the biosynthesis of MPO and TPO as well as the impact of inherited mutations in the MPO gene on normal biosynthesis will be summarized. Lastly, specific gaps in our knowledge revealed by this review of our current understanding will be highlighted.

Indexed as

Binding SitesCalciumDimerizationEndoplasmic ReticulumEosinophil PeroxidaseGlycosylationHemeHumansIodide PeroxidaseLactoperoxidasePeroxidaseProteolysisCalciumEosinophil PeroxidaseHemeIodide PeroxidaseLactoperoxidasePeroxidaseCyclooxygenase-peroxidase protein familyHeme proteinsMyeloperoxidasePeroxidases

Identifiers

PMID29408362
PMCPMC5967637
OpenAlexW2788405691

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.