Evidence map›Paper›PMID 17970228›Full record

ReviewInfectious disorders drug targets2007

Targeting the formation of the cell wall core of M. tuberculosis.

Clifton E Barry, Dean C Crick, Michael R McNeil

Open access · greenAbstract readReview
In one paragraph

Review in Infectious disorders drug targets, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

47 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. Article
  3. Structural basis for the development of potential inhibitors targeting FadD23 from Mycobacterium tuberculosis.Acta crystallographica. Section F, Structural biology communications · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. TheFrontiers in cellular and infection microbiology · 2021
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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 2 institutions in 1 country.

Clifton E BarryTuberculosis Research Section, Laboratory of Clinical Infectious Disease, NIAID, NIH, 33 North Drive Bldg 33, Room 2W20D Bethesda, MD 20892, USA.
Dean C Crick
Michael R McNeil
Colorado State University · USNational Institutes of Health · US

Funding

Vascular stabilization as a broad theraprutic platform for biodefenseU54AI065357 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI SLAYDEN, RICHARD A · 2005 to 2013
$77.5M
Pathogenesis, Latency and Drug Resistance Of Mycobacterium TuberculosisZ01AI000783 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI BARRY, CLIFTON · 1997 to 2008
$5.8M
Structure of enzymes in Multi-Drug Resistant Tuberculosis (MDR-TB)P01AI057836 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI LENAERTS, ANNE J. · 2004 to 2008
$4.5M
Sterol/Hopanoid Biosynthesis: An Anti-TB Drug TargetR01AI049151 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI CRICK, DEAN C · 2001 to 2019
$4.1M
CELL WALL BIOGENESIS: TARGET FOR NEW ANTI-TB DRUGSR01AI033706 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI MCNEIL, MICHAEL R · 1992 to 2006
$2.5M
TB DRUGS VIA INHIBITORS OF CELL WALL SYNTHETIC ENZYMESP01AI046393 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI BRENNAN, PATRICK JOSEPH · 1999 to 2002
$2.2M
HTS assays for the methylerythritol-4-phosphate pathwayR01AI097550 · NIAID · COLORADO STATE UNIVERSITY · PI CRICK, DEAN C · 2012 to 2014
$1.1M
Menaquinone biosynthesis: a drug target in Gram-positive bacteriaR56AI049151 · NIAID · COLORADO STATE UNIVERSITY · PI CRICK, DEAN C · 2007 to 2007
$320k
Intramural NIH HHS Z01 AI000783NIAID NIH HHS AI049151NIAID NIH HHS AI057836NIAID NIH HHS AI065357-020010NIAID NIH HHS AI33706NIAID NIH HHS P01 AI046393NIAID NIH HHS P01 AI057836NIAID NIH HHS R01 AI033706NIAID NIH HHS R01 AI049151NIAID NIH HHS R01 AI097550NIAID NIH HHS R56 AI049151NIAID NIH HHS U54 AI065357
6 · The paper itself

Abstract

Mycobacteria have a unique cell wall, which is rich in drug targets. The cell wall core consists of a peptidoglycan layer, a mycolic acid layer, and an arabinogalactan polysaccharide connecting them. The detailed structure of the cell wall core is largely, although not completely, understood and will be presented. The biosynthetic pathways of all three components reveal significant drug targets that are the basis of present drugs and/or have potential for new drugs. These pathways will be reviewed and include enzymes involved in polyisoprene biosynthesis, soluble arabinogalactan precursor production, arabinogalactan polymerization, fatty acid synthesis, mycolate maturation, and soluble peptidoglycan precursor formation. Information relevant to targeting all these enzymes will be presented in tabular form. Selected enzymes will then be discussed in more detail. It is thus hoped this chapter will aid in the selection of targets for new drugs to combat tuberculosis.

Indexed as

Antitubercular AgentsCell WallGalactansMycobacterium tuberculosisMycolic AcidsPeptidoglycanPolyisoprenyl PhosphatesAntitubercular Agentsarabinogalactandecaprenyl phosphateGalactansMycolic AcidsPeptidoglycanPolyisoprenyl Phosphates

Identifiers

PMID17970228
PMCPMC4747060
OpenAlexW2272837046

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.