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Multiple Helicobacter pylori proteins and enzymes

Molecular classification
Enzyme, Transporter, Binding protein, Protease, Adhesin, Oxidoreductase, Other
01

Overview

Multiple Helicobacter pylori proteins and enzymes" refers to a collection of molecular entities that are essential for the survival, colonization, and pathogenicity of Helicobacter pylori, a bacterium implicated in gastric ulcers, gastritis, and gastric cancer. These include enzymes such as urease (key for acid resistance in the stomach), superoxide dismutase and catalase (oxidative stress resistance), thioredoxins, various proteases, and metabolic enzymes involved in amino acid biosynthesis and central metabolism. Several core proteins (e.g., those conserved across H. pylori strains) are being explored as potential drug targets due to their essentiality and specificity to the pathogen, with the aim of developing novel therapeutics, particularly in the context of increasing antibiotic resistance. H. pylori also possesses unique proteins for metal ion trafficking (notably nickel), which are critical for enzyme function and may be leveraged for therapeutic intervention. Collectively, targeting multiple essential proteins and enzymes offers promising avenues for safe and specific eradication of H. pylori infections[2][4][5][6].

Other names
H. pylori proteinsH. pylori enzymesHelicobacter pylori molecular targets
02

Mechanism of action

Enzyme inhibition (urease, aspartate α-decarboxylase) [4][6]; Membrane disruption (antimicrobial peptides, bacteriocins) [6]; Blocking bacterial adhesion to host tissues (e.g., by inhibiting adhesins or using specific peptides) [6]; Inhibition of nickel handling and storage (targeting nickel-binding proteins) [5]; Interference in metabolic pathways (targeting essential bacterial enzymes) [2][3][4]

03

Biological functions

MetabolismAcid tolerance (urease activity)Oxidative stress resistance (superoxide dismutase, catalase)Protein folding (thioredoxin, thioredoxin reductase)Nickel homeostasis (nickel-binding proteins)Cell wall modification (autolytic enzyme/lysozyme)Pathogen-host interaction (adhesins, outer membrane proteins)Other
04

Disease associations

InfectionGastric cancer (via chronic infection)Peptic ulcer diseaseInflammationAntibiotic resistanceOther
05

Safety considerations

Off-target effects due to similarity with human metabolic or mitochondrial proteins (relevant for enzymes with homologs) [2]Risk of resistance development (for some enzymatic targets, though aspartate α-decarboxylase less so) [4][6]Microbiota disruption (broad-spectrum agents) [6]Cytotoxicity of some antimicrobials (must be evaluated) [4]
06

Interacting drugs

Malonic acid (inhibitor of aspartate α-decarboxylase) [4]

4 more in the full profile.

07

Biomarkers

Urease activity (diagnostic marker for H. pylori)

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