Evidence map›Paper›PMID 31312014›Full record

ArticleScientific reports2019

Mechanism of catalysis and inhibition of Mycobacterium tuberculosis SapM, implications for the development of novel antivirulence drugs.

Paulina Fernandez-Soto, Alexander J E Bruce, Alistair J Fielding, Jennifer S Cavet, Lydia Tabernero

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Delayed-Type Hypersensitivity toInternational journal of molecular sciences · 2026
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Secreted proteins ofFrontiers in tuberculosis · 2026
    Review
  6. Article
  7. ESX-5 Deletions inbioRxiv : the preprint server for biology · 2025
    Article
  8. TowardMicroorganisms · 2024
    Review
  9. Combating Tuberculosis via Restoring the Host Immune Capacity by TargetingInternational journal of molecular sciences · 2024
    Review
  10. Article
  11. Review
  12. Different modalities of host cell death and their impact onAmerican journal of physiology. Cell physiology · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Rv2577 ofFrontiers in microbiology · 2020
    Article
  17. 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

5 authors at 2 institutions in 1 country.

Paulina Fernandez-SotoSchool of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.ORCID http://orcid.org/0000-0002-8224-1902
Alexander J E BruceSchool of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Alistair J FieldingPharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool, L3 3AF, UK.ORCID http://orcid.org/0000-0002-4437-9791
Jennifer S CavetSchool of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Lydia TaberneroSchool of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK. Lydia.Tabernero@manchester.ac.uk.ORCID http://orcid.org/0000-0001-8867-455X
Manchester Academic Health Science Centre · GBLiverpool John Moores University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb) SapM is a secreted virulence factor critical for intracellular survival of the pathogen. The role of SapM in phagosome maturation arrest in host macrophages suggests its potential as a drug target to assist in the clearance of tuberculosis infection. However, the mechanism of action of SapM at the molecular level remains unknown. In this study, we provide new insights into the mechanism of catalysis, substrate specificity and inhibition of SapM, and we identify the critical residues for catalysis and substrate binding. Our findings demonstrate that SapM is an atypical monoester alkaline phosphatase, with a serine-based mechanism of catalysis probably metal-dependent. Particularly relevant to SapM function and pathogenesis, is its activity towards PI(4,5)P

Indexed as

Acid PhosphataseAntitubercular AgentsAscorbic AcidBacterial ProteinsCatalysisCatalytic DomainHumansInhibitory Concentration 50Mycobacterium tuberculosisPhosphatidylinositolsSubstrate SpecificityTHP-1 CellsVirulenceAcid PhosphataseAntitubercular Agentsascorbate-2-phosphateAscorbic AcidBacterial ProteinsPhosphatidylinositols

Identifiers

PMID31312014
PMCPMC6635428
OpenAlexW2958048043

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.