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Explore antimicrobial resistance genes from the literature
K+ uptake protein
Overview
| Protein Change | Nucleotide Change | Mechanism | Organism | Resistance To | Database | Validation Status |
|---|---|---|---|---|---|---|
| Q26* | - | - | Clostridioides difficile | Vancomycin | Reslit | Candidate |
| Allele | Database | Papers | Drug Classes | Organisms | Countries | Years | Sequence Accession |
|---|
| Protein Accession |
|---|
| trkA | Reslit | 3 | Polymyxin b, Piperacillin +4 | Vibrio vulnificus +2 | - | 2004, 2009, 2016 | AY293743 | - |
| TrkA | Reslit | 1 | - | Vibrio vulnificus | - | - | - | - |
A K+ Uptake Protein, TrkA, Is Required for Serum, Protamine, and Polymyxin B Resistance in Vibrio vulnificus.
The study identifies TrkA as a K+ uptake protein required for resistance to serum, protamine, and polymyxin B in Vibrio vulnificus. Mutants lacking trkA show reduced resistance to these agents.
Genetic architecture of intrinsic antibiotic susceptibility.
The study identifies multiple genes and mutations that contribute to antibiotic tolerance in E. coli, revealing a large mutational target size for increasing drug resistance. Key findings include the role of genes involved in electron transport, flagella synthesis, and efflux pumps in modulating susceptibility to various antibiotics.
Antimicrobial Peptides and Their Mechanisms of Action Against Pathogens
Genome-Wide Identification of Antimicrobial Intrinsic Resistance Determinants in Staphylococcus aureus.
The study identifies multiple intrinsic resistance determinants in Staphylococcus aureus, including genes such as atpA, rpsT, vraG, and mecA, which contribute to resistance against various antimicrobial agents. These findings highlight potential targets for developing antimicrobial potentiators.
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