Target intelligence / Profile preview

Arabinofuranosyltransferase EmbC (EmbC) (EmbC)

Target
EmbC
Molecular classification
Enzyme, Glycosyltransferase, Membrane protein, Glycosyltransferase C superfamily
01

Overview

Arabinofuranosyltransferase EmbC (EmbC) is a membrane-bound enzyme belonging to the glycosyltransferase C superfamily, primarily found in mycobacteria such as Mycobacterium tuberculosis (UniProt, 2024; InterPro, 2024). It plays a critical role in the biosynthesis of the mycobacterial cell wall by catalyzing the polymerization of the arabinan domain of lipoarabinomannan (LAM), a key lipoglycan involved in host-pathogen interactions and immune modulation (NIH, 2014; PubMed, 2009). Unlike its counterparts EmbA and EmbB, which are mainly involved in arabinogalactan synthesis, EmbC is specifically dedicated to LAM assembly (Nature, 2020; NIH, 2014). As an essential gene in M. tuberculosis, EmbC is a validated therapeutic target for the frontline antitubercular drug ethambutol, which inhibits its activity and leads to cell wall instability and bacterial death (FDA, 2024; PubMed, 2009). Mutations in the embC gene or the broader embCAB operon are frequently associated with ethambutol resistance in clinical isolates (NIH, 2019; PubMed, 2009). Understanding the structure and function of EmbC is vital for developing next-generation antitubercular agents that can overcome existing resistance mechanisms (ResearchGate, 2011; NIH, 2022).

Other names
Arabinofuranosyl transferase EmbCArabinosyltransferase CEmbCArabinofuranosyltransferase C
02

Mechanism of action

Ethambutol inhibits the arabinosyltransferase activity of EmbC by competing with the donor substrate decaprenylphosphoryl-arabinose (DPA), thereby blocking the synthesis of lipoarabinomannan (LAM) and disrupting the mycobacterial cell wall (NIH, 2014; PubMed, 2009).

03

Biological functions

Cell wall biosynthesisLipoarabinomannan (LAM) biosynthesisArabinan polymerizationHost-pathogen interaction modulation
04

Disease associations

InfectionTuberculosis
05

Safety considerations

Development of drug-resistant tuberculosis (MDR-TB)Ocular toxicity (optic neuritis) associated with ethambutol treatmentEssentiality in Mycobacterium tuberculosis makes it a critical but challenging target for drug development
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Interacting drugs

Ethambutol
07

Biomarkers

embC gene mutationsembB gene mutationsembCAB operon polymorphismsTruncated lipoarabinomannan (LAM) species

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