Inducible auto-phosphorylation regulates a widespread family of nucleotidyltransferase toxins.

Inducible auto-phosphorylation regulates a widespread family of nucleotidyltransferase toxins.

Publication date: Sep 04, 2024

Nucleotidyltransferases (NTases) control diverse physiological processes, including RNA modification, DNA replication and repair, and antibiotic resistance. The Mycobacterium tuberculosis NTase toxin family, MenT, modifies tRNAs to block translation. MenT toxin activity can be stringently regulated by diverse MenA antitoxins. There has been no unifying mechanism linking antitoxicity across MenT homologues. Here we demonstrate through structural, biochemical, biophysical and computational studies that despite lacking kinase motifs, antitoxin MenA induces auto-phosphorylation of MenT by repositioning the MenT phosphoacceptor T39 active site residue towards bound nucleotide. Finally, we expand this predictive model to explain how unrelated antitoxin MenA is similarly able to induce auto-phosphorylation of cognate toxin MenT. Our study reveals a conserved mechanism for the control of tuberculosis toxins, and demonstrates how active site auto-phosphorylation can regulate the activity of widespread NTases.

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Concepts Keywords
Auto Bacterial Proteins
Biophysical Bacterial Proteins
Nucleotidyltransferase Bacterial Toxins
Predictive Bacterial Toxins
Tuberculosis Catalytic Domain
Crystallography, X-Ray
Models, Molecular
Mycobacterium tuberculosis
Nucleotidyltransferases
Nucleotidyltransferases
Phosphorylation
RNA, Transfer
RNA, Transfer

Semantics

Type Source Name
pathway REACTOME DNA Replication
disease IDO antibiotic resistance
disease IDO toxin
drug DRUGBANK Trestolone
pathway REACTOME Translation
disease IDO site
disease MESH tuberculosis
pathway KEGG Tuberculosis
disease IDO replication
disease IDO bacteria
disease IDO virulence
disease IDO protein
disease IDO pathogen
disease MESH infection
disease IDO production
drug DRUGBANK Phosphate ion
drug DRUGBANK Sodium lauryl sulfate
drug DRUGBANK Aspartame
drug DRUGBANK Naproxen
drug DRUGBANK Magnesium
drug DRUGBANK ATP
drug DRUGBANK Oxygen
drug DRUGBANK Nitrogen
drug DRUGBANK Phosphorus
disease IDO cell
drug DRUGBANK Glycine
drug DRUGBANK Coenzyme M
drug DRUGBANK L-Threonine
drug DRUGBANK Piroxicam
drug DRUGBANK Water
drug DRUGBANK Proline
disease IDO assay
drug DRUGBANK Cytidine
drug DRUGBANK Timonacic
drug DRUGBANK Adenine
drug DRUGBANK L-Lysine
drug DRUGBANK Glutamic Acid
drug DRUGBANK Isopropyl beta-D-thiogalactopyranoside
disease MESH repression

Original Article

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