Evidence map›Paper›PMID 33319550›Full record

ArticleACS infectious diseases2021

Two-Way Regulation of MmpL3 Expression Identifies and Validates Inhibitors of MmpL3 Function in

Shipra Grover, Curtis A Engelhart, Esther Pérez-Herrán, Wei Li, Katherine A Abrahams, Kadamba Papavinasasundaram, James M Bean, Christopher M Sassetti, Alfonso Mendoza-Losana, Gurdyal S Besra and 2 more

Open access · hybridAbstract read
In one paragraph

Article in ACS infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.3field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Structural isomerisation affects the antitubercular activity of adamantyl-isoxyl adducts.Journal of enzyme inhibition and medicinal chemistry · 2025
    Article
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  4. Common Biological Properties ofACS infectious diseases · 2025
    Article
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  8. Article
  9. TheMicrobiology spectrum · 2024
    Article
  10. Article
  11. Review
  12. Molecular Mechanisms of MmpL3 Function and Inhibition.Microbial drug resistance (Larchmont, N.Y.) · 2023
    Review
  13. Article
  14. The driving force for mycolic acid export by mycobacterial MmpL3 is proton translocation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
  16. 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

12 authors at 6 institutions in 3 countries.

Shipra GroverDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, New York 10065, United States.ORCID 0000-0001-7094-6879
Curtis A EngelhartDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, New York 10065, United States.
Esther Pérez-HerránTB Research Unit, Global Health R&D, GlaxoSmithKline, Severo Ochoa 2, Tres Cantos, Madrid 28760, Spain.
Wei LiMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523, United States.
Katherine A AbrahamsInstitute of Microbiology and Infection, School of Biological Sciences, University of Birmingham, Birmingham B15 2TT, U.K.
Kadamba PapavinasasundaramDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts 01655, United States.
James M BeanSloan Kettering Institute, New York, New York 10065, United States.
Christopher M SassettiDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts 01655, United States.
Alfonso Mendoza-LosanaTB Research Unit, Global Health R&D, GlaxoSmithKline, Severo Ochoa 2, Tres Cantos, Madrid 28760, Spain.
Gurdyal S BesraInstitute of Microbiology and Infection, School of Biological Sciences, University of Birmingham, Birmingham B15 2TT, U.K.ORCID 0000-0002-5605-0395
Mary JacksonMycobacteria Research Laboratories, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523, United States.ORCID 0000-0002-9212-0258
Dirk SchnappingerDepartment of Microbiology and Immunology, Weill Cornell Medicine, New York, New York 10065, United States.
Cornell University · USColorado State University · USGlaxoSmithKline (Spain) · ESUniversity of Birmingham · GBUniversity of Massachusetts Chan Medical School · USKettering University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Viable but Nonculturable MtbU19AI111143 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI GLICKMAN, MICHAEL HAGGAI, GLICKMAN, MICHAEL S · 2014 to 2020
$48.6M
MmpL3 as a target for novel anti-TB agentsR01AI116525 · NIAID · COLORADO STATE UNIVERSITY · PI JACKSON, MARY · 2015 to 2024
$5.3M
Medical Research Council MR/R001154/1Medical Research Council MR/S000542/1NCI NIH HHS P30 CA008748NIAID NIH HHS R01 AI116525NIAID NIH HHS U19 AI111143
6 · The paper itself

Abstract

MmpL3, an essential mycolate transporter in the inner membrane of

Indexed as

Bacterial ProteinsMembrane Transport ProteinsMycobacterium tuberculosisAntitubercular AgentsMycolic AcidsAntitubercular AgentsBacterial ProteinsMembrane Transport ProteinsMmpL3 protein, Mycobacterium tuberculosisMycolic Acidsantibioticsdrug discoverymolecular geneticsmycolic acidsrespirationtargeted whole-cell screen

Identifiers

PMID33319550
PMCPMC7802072
OpenAlexW3177715446

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.