Evidence map›Paper›PMID 27663982›Full record

ReviewCold Spring Harbor perspectives in medicine2016

Approved Glycopeptide Antibacterial Drugs: Mechanism of Action and Resistance.

Daina Zeng, Dmitri Debabov, Theresa L Hartsell, Raul J Cano, Stacy Adams, Jessica A Schuyler, Ronald McMillan, John L Pace

Open access · bronzeAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

111 citing papers in PubMed, 3 syntheses or guidelines pooled it, 200 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Discovery and Biosynthesis of the Novel Glycotetrapeptide Antibiotic Biffamycin A.Angewandte Chemie (International ed. in English) · 2026
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Frontiers in medicine · 2026
    Article
  14. Review
  15. Review
  16. Antibiotic-Induced Bacterial Cell Death: A "Radical" Way of Dying?Current topics in microbiology and immunology · 2025
    Article
  17. Review
  18. Review
  19. Article
  20. Review

51 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

8 authors at 6 institutions in 3 countries.

Daina ZengAgile Sciences, Raleigh, North Carolina 27606.
Dmitri DebabovEmery Pharma Services, Emeryville, California 94608.
Theresa L HartsellDepartment of Anesthesiology/Critical Care Medicine, The Johns Hopkins School of Medicine and Nursing, Baltimore, Maryland 21287.
Raul J CanoATCC Center for Translational Microbiology, Union, New Jersey 07083.
Stacy AdamsCenter for Skin Biology, GlaxoSmithKline, Durham, North Carolina 27703.
Jessica A SchuylerATCC Center for Translational Microbiology, Union, New Jersey 07083.
Ronald McMillanATCC Center for Translational Microbiology, Union, New Jersey 07083.
John L PaceATCC Center for Translational Microbiology, Union, New Jersey 07083.
Center for Translational Molecular Medicine · NLAdamas Pharmaceuticals (United States) · USAgile Sciences (United States) · USGlaxoSmithKline (United States) · USJohns Hopkins University · USNorth Carolina Central University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The glycopeptide antimicrobials are a group of natural product and semisynthetic glycosylated peptides that show antibacterial activity against Gram-positive organisms through inhibition of cell-wall synthesis. This is achieved primarily through binding to the d-alanyl-d-alanine terminus of the lipid II bacterial cell-wall precursor, preventing cross-linking of the peptidoglycan layer. Vancomycin is the foundational member of the class, showing both clinical longevity and a still preferential role in the therapy of methicillin-resistant Staphylococcus aureus and of susceptible Enterococcus spp. Newer lipoglycopeptide derivatives (telavancin, dalbavancin, and oritavancin) were designed in a targeted fashion to increase antibacterial activity, in some cases through secondary mechanisms of action. Resistance to the glycopeptides emerged in delayed fashion and occurs via a spectrum of chromosome- and plasmid-associated elements that lead to structural alteration of the bacterial cell-wall precursor substrates.

Indexed as

Drug Resistance, BacterialAnti-Bacterial AgentsCell WallGlycopeptidesMethicillin-Resistant Staphylococcus aureusVancomycin-Resistant EnterococciAnti-Bacterial AgentsGlycopeptides

Identifiers

PMID27663982
PMCPMC5131748
OpenAlexW2522642005

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.