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Arabinosyl transferase enzyme complex (null)

Target
null
Molecular classification
Enzyme, Glycosyltransferase (specifically, GT-C fold family), Membrane-bound enzyme
01

Overview

The Arabinosyl transferase enzyme complex refers to a family of integral membrane glycosyltransferases, including proteins like EmbA, EmbB, EmbC, and AftA, which are essential for the assembly of the arabinan component of arabinogalactan and lipoarabinomannan in the mycobacterial cell wall[1][2][3][4][9]. These enzymes catalyze the transfer of arabinose residues from decaprenylphosphoryl-arabinose (DPA) donors to polysaccharide acceptors via specific glycosidic linkages, supporting the structural integrity and function of the cell envelope in *Mycobacterium tuberculosis*[1][4]. They are validated therapeutic targets, as inhibition by drugs like ethambutol impairs cell wall construction and leads to bactericidal effects[1][3][6]. The term "Arabinosyl transferase enzyme complex" sometimes refers specifically to an *enzyme dimer* (e.g., EmbB~2~-AcpM~2~) or broadly to the functional set of related enzymes[1][2]. The best-characterized clinical target is EmbB, especially for ethambutol, but other family members (EmbA, EmbC, AftA) play non-redundant, essential roles in cell wall biosynthesis in mycobacteria[1][2][3][5][6].

Other names
Emb protein complexEmbA-EmbB-EmbC complexarabinofuranosyltransferase complexAG arabinosyltransferasearabinofuranosyltransferase (family includes EmbA, EmbB, EmbC, AftA, AftB)
02

Mechanism of action

Ethambutol inhibits these arabinosyltransferases by binding to the same site as their natural substrates and blocking arabinose transfer, thus disrupting cell wall synthesis and compromising bacterial viability[1][3][5][6].

03

Biological functions

Cell wall biosynthesis (arabinan and arabinogalactan assembly)Polysaccharide polymerization
04

Disease associations

Infection (crucial for viability and virulence of *Mycobacterium tuberculosis*)Important determinant in tuberculosis (TB) pathogenesis and drug resistance
05

Safety considerations

No notable human safety concerns are associated with the bacterial enzyme complex itself (these are prokaryotic enzymes).For therapeutics: rapid development of resistance (notably via EmbB mutations) and potential cross-resistance with new agents targeting the same site[6].
06

Interacting drugs

Ethambutol (EMB)
07

Biomarkers

Mutations in EmbB/EmbC confer ethambutol resistance; such mutations can serve as markers for drug-resistant TB strains[1][5][6].

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