Evidence map›Paper›PMID 20932952›Full record

ReviewArchives of biochemistry and biophysics2011

Enzymes of the mevalonate pathway of isoprenoid biosynthesis.

Henry M Miziorko

Abstract readReview
In one paragraph

Review in Archives of biochemistry and biophysics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 199 papers.

0numbers the graph read from it
0cells of the map it votes in
199citing papers in PubMed
9.2field-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

199 citing papers in PubMed, 472 citations in OpenAlex.

  1. Menaquinone biosynthesis inEngineering microbiology · 2026
    Review
  2. Synthetic and systems biotechnology · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Metabolomics reveal drought-stress responses in guayule, a semi-arid rubber crop.Metabolomics : Official journal of the Metabolomic Society · 2026
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Microbial conversion of biodiesel waste for carotenoid production.Frontiers in bioengineering and biotechnology · 2026
    Article
  18. Article
  19. Article
  20. Review

139 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

1 author at 1 institution in 1 country.

Henry M MiziorkoUniversity of Missouri - Kansas City, 64110, USA. miziorkoh@umkc.edu
University of Missouri–Kansas City · US

Funding

HMG-COA CYCLE CONTROL IN NORMAL AND DIABETIC LIVERR01DK021491 · NIDDK · UNIVERSITY OF MISSOURI KANSAS CITY · PI MIZIORKO, HENRY M · 1986 to 2004
$1.6M
MEVALONATED METABOLIZING ENZYMES &THEIR INBORN DEFECTSR01DK053766 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI KIM, JUNG JA P. · 1998 to 2003
$732k
HMG-COA CYCLE CONTROL IN NORMAL AND DIABETIC LIVERR37DK021491 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI MIZIORKO, HENRY M · 1991 to 1999
–
NIDDK NIH HHS DK21491NIDDK NIH HHS DK53766NIDDK NIH HHS R01 DK021491NIDDK NIH HHS R01 DK053766NIDDK NIH HHS R37 DK021491
6 · The paper itself

Abstract

The mevalonate pathway accounts for conversion of acetyl-CoA to isopentenyl 5-diphosphate, the versatile precursor of polyisoprenoid metabolites and natural products. The pathway functions in most eukaryotes, archaea, and some eubacteria. Only recently has much of the functional and structural basis for this metabolism been reported. The biosynthetic acetoacetyl-CoA thiolase and HMG-CoA synthase reactions rely on key amino acids that are different but are situated in active sites that are similar throughout the family of initial condensation enzymes. Both bacterial and animal HMG-CoA reductases have been extensively studied and the contrasts between these proteins and their interactions with statin inhibitors defined. The conversion of mevalonic acid to isopentenyl 5-diphosphate involves three ATP-dependent phosphorylation reactions. While bacterial enzymes responsible for these three reactions share a common protein fold, animal enzymes differ in this respect as the recently reported structure of human phosphomevalonate kinase demonstrates. There are significant contrasts between observations on metabolite inhibition of mevalonate phosphorylation in bacteria and animals. The structural basis for these contrasts has also recently been reported. Alternatives to the phosphomevalonate kinase and mevalonate diphosphate decarboxylase reactions may exist in archaea. Thus, new details regarding isopentenyl diphosphate synthesis from acetyl-CoA continue to emerge.

Indexed as

AnimalsEnzyme InhibitorsEnzymesHumansMevalonic AcidTerpenesEnzyme InhibitorsEnzymesMevalonic AcidTerpenes

Identifiers

PMID20932952
PMCPMC3026612
OpenAlexW1994675489

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.