| Accession | ARO:3000746 |
| CARD Short Name | mepR |
| Definition | MepR is an upstream repressor of MepA in Staphylococcus aureus. It is part of the mepRAB operon. |
| AMR Gene Family | multidrug and toxic compound extrusion (MATE) transporter |
| Drug Class | tetracycline antibiotic, glycylcycline |
| Resistance Mechanism | antibiotic efflux |
| Efflux Component | efflux pump complex or subunit conferring antibiotic resistance |
| Efflux Regulator | protein(s) and two-component regulatory system modulating antibiotic efflux |
| Resistomes with Perfect Matches | Staphylococcus aureusg+p+wgs |
| Resistomes with Sequence Variants | Escherichia coliwgs, Klebsiella pneumoniaewgs, Staphylococcus aureusg+p+wgs, Staphylococcus epidermidiswgs |
| Classification | 10 ontology terms | Show + process or component of antibiotic biology or chemistry + antibiotic molecule + mechanism of antibiotic resistance + antibiotic efflux [Resistance Mechanism] + tetracycline antibiotic [Drug Class] + determinant of antibiotic resistance + efflux pump complex or subunit conferring antibiotic resistance [Efflux Component] + glycylcycline [Drug Class] + tigecycline [Antibiotic] + multidrug and toxic compound extrusion (MATE) transporter [AMR Gene Family] |
| Parent Term(s) | 2 ontology terms | Show + regulates mepA + protein(s) and two-component regulatory system modulating antibiotic efflux [Efflux Regulator] |
| Publications | McAleese F, et al. 2005. Antimicrob Agents Chemother 49(5): 1865-1871. A novel MATE family efflux pump contributes to the reduced susceptibility of laboratory-derived Staphylococcus aureus mutants to tigecycline. (PMID 15855508) Kaatz GW, et al. 2006. Antimicrob Agents Chemother 50(4): 1276-1281. MepR, a repressor of the Staphylococcus aureus MATE family multidrug efflux pump MepA, is a substrate-responsive regulatory protein. (PMID 16569840) Kaatz GW, et al. 2005. Antimicrob Agents Chemother 49(5): 1857-1864. Multidrug resistance in Staphylococcus aureus due to overexpression of a novel multidrug and toxin extrusion (MATE) transport protein. (PMID 15855507) |
Prevalence of mepR among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 263 important pathogens (see methodological details and complete list of analyzed pathogens). Values reflect percentage of genomes, plasmids, genome islands, or whole-genome shotgun assemblies that have at least one hit to the AMR detection model. Default view includes percentages calculated based on Perfect plus Strict RGI hits. Select the checkbox to view percentages based on only Perfect matches to AMR reference sequences curated in CARD (note: this excludes resistance via mutation as references in protein variant models are often wild-type, sensitive sequences).
| Species | NCBI Chromosome | NCBI Plasmid | NCBI WGS | NCBI GI |
|---|---|---|---|---|
| Escherichia coli | 0% | 0% | 0.02% | 0% |
| Klebsiella pneumoniae | 0% | 0% | 0.01% | 0% |
| Staphylococcus aureus | 99.63% | 0.12% | 61.13% | 0% |
| Staphylococcus epidermidis | 0% | 0% | 0.1% | 0% |
Model Type: protein homolog model
Model Definition: The protein homolog model is an AMR detection model. Protein homolog models detect a protein sequence based on its similarity to a curated reference sequence. A protein homolog model has only one parameter: a curated BLASTP bitscore cutoff for determining the strength of a match. Protein homolog model matches to reference sequences are categorized on three criteria: perfect, strict and loose. A perfect match is 100% identical to the reference sequence along its entire length; a strict match is not identical but the bitscore of the matched sequence is greater than the curated BLASTP bitscore cutoff. Loose matches are other sequences with a match bitscore less than the curated BLASTP bitscore.
Bit-score Cut-off (blastP): 250