lmrA

Accession ARO:3003028
CARD Short NamelmrA
DefinitionlmrA is the repressor to the lmrAB operon in Bacillus subtilis. lmrA mutations result in lincomycin resistance.
AMR Gene FamilyATP-binding cassette (ABC) antibiotic efflux pump
Drug Classnucleoside antibiotic, lincosamide antibiotic
Resistance Mechanismantibiotic efflux, antibiotic target alteration
Efflux Componentefflux pump complex or subunit conferring antibiotic resistance
Efflux Regulatorprotein(s) and two-component regulatory system modulating antibiotic efflux
Classification15 ontology terms | Show
Parent Term(s)3 ontology terms | Show
Publications

Yoshida K, et al. 2004. J Bacteriol 186(17): 5640-5648. Bacillus subtilis LmrA is a repressor of the lmrAB and yxaGH operons: identification of its binding site and functional analysis of lmrB and yxaGH. (PMID 15317768)

Kunst F, et al. 1997. Nature 390(6657): 249-256. The complete genome sequence of the gram-positive bacterium Bacillus subtilis. (PMID 9384377)

Resistomes

Prevalence of lmrA among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 413 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).

Prevalence: protein variant model

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GI
No prevalence data


Detection Models

Model Type: protein variant model

Model Definition: Protein Variant Models (PVM) perform a similar search as Protein Homolog Models (PHM), i.e. detect protein sequences based on their similarity to a curated reference sequence, but secondarily screen query sequences for curated sets of mutations to differentiate them from antibiotic susceptible wild-type alleles. PVMs are designed to detect AMR acquired via mutation of house-keeping genes or antibiotic targets, e.g. a mutated gyrase resistant to aminocoumarin antibiotics. PVMs include a protein reference sequence (often from antibiotic susceptible wild-type alleles), a curated bit-score cut-off, and mapped resistance variants. Mapped resistance variants may include any or all of single point mutations, insertions, or deletions curated from the scientific literature. A Strict RGI match has a BLASTP bit-score above the curated BLASTP cutoff value and contains at least one curated mutation from amongst the mapped resistance variants, while a Loose RGI match has a bit-score less than the curated BLASTP bit-score cut-off but still contains at least one curated mutation from amongst the mapped resistance variants.

Bit-score Cut-off (blastP): 900

Legend:

  • discovered in clinical, agricultural, or environmental isolates

  • discovered via laboratory selection experiments

  • ReSeqTB https://platform.reseqtb.org

Published Variants:


>gb|CAA42550.1|+|lmrA [Streptomyces lincolnensis]
MSVFARATSLFSRAARTRAADEAARSRSRWVTLVFLAVLQLLIAVDVTVVNIALPAIRDS
FHVDTRQLTWVVTGYTVVGGGLLMVGGRIADLFGRRRTLLFGAFLFGASSLAAGLAPNLE
LLVLARFGQGAGEALSLPAAMSLIACSSRTAPFQGVERLASVASVGLVLGFLLSGVITQL
FSWRWIFLINIPLVSLVLVAVLLLVKKDETTARNPVDLPGALLFTAAPLLLIFGVNELGE
DEPRLPLAVGSLLAAAVCAAAFVAVERRTAHPLVPLTFFGNRVRLVANGATVLLSAALST
SFFLLTMHLQEERDLSPIEAGLSFLPLGLSLILACVLVRGLIERIGTTGAAVLGMALAGP
RHRLFALLPSDNSLLTSVFPGMILLLRMATGLVALQNAALHAVTEADAGVASGVQRCADQ
LGGASGIAVYVSIGFSPHLGGDWDPFTVAYSLAGIGLIAAVLAVLALSPDRRLAAPREQE
D



>gb|X59926.1|+|318-1763|lmrA [Streptomyces lincolnensis]
ATGTCTGTCTTCGCTCGTGCCACCTCGCTCTTCTCCCGTGCCGCGCGGACCCGCGCGGCCGATGAGGCGGCCCGTTCCCGGTCTCGCTGG
GTCACCCTCGTCTTCCTCGCCGTGCTCCAGCTCCTCATCGCGGTCGACGTGACCGTAGTGAACATCGCCCTGCCTGCGATCCGCGACAGC
TTCCACGTCGACACCCGTCAACTCACCTGGGTAGTCACGGGTTACACCGTCGTGGGCGGCGGCCTGCTCATGGTGGGCGGGCGCATCGCC
GACCTCTTCGGGCGGCGCCGGACCCTCCTTTTCGGGGCCTTCCTCTTCGGTGCGTCGTCCCTCGCCGCGGGCCTCGCCCCGAACCTGGAG
CTGCTCGTGCTCGCACGGTTCGGGCAGGGCGCAGGAGAGGCCCTCTCCCTGCCGGCCGCGATGTCGCTCATCGCCTGCTCTTCCCGAACC
GCGCCGTTCCAAGGCGTTGAGCGTCTGGCGTCGGTCGCCAGCGTCGGCCTCGTCCTCGGCTTCCTGCTCTCCGGGGTCATCACCCAGCTC
TTCAGCTGGCGTTGGATCTTCCTGATCAACATCCCCCTCGTCAGCCTCGTGCTCGTCGCCGTACTGCTGCTGGTCAAGAAGGACGAGACG
ACCGCACGCAATCCCGTCGACCTCCCCGGCGCGCTCCTCTTCACGGCCGCGCCGCTGCTGCTCATCTTCGGCGTCAACGAGCTGGGCGAG
GACGAGCCCCGGCTGCCGCTCGCCGTCGGGAGCCTGCTCGCGGCCGCGGTGTGCGCGGCCGCGTTCGTCGCCGTCGAGCGGCGCACGGCC
CATCCCCTGGTTCCCCTGACGTTCTTCGGGAACCGCGTCCGCCTGGTCGCCAACGGCGCCACGGTCCTCCTCAGCGCCGCCCTCTCGACC
TCCTTCTTCCTGCTGACCATGCACTTGCAGGAGGAGCGCGACCTGTCCCCCATCGAGGCGGGACTGTCCTTCCTGCCCCTGGGCCTCAGC
CTCATCCTCGCCTGCGTCCTCGTCCGGGGCCTCATCGAGCGCATCGGCACCACCGGCGCGGCGGTGCTCGGCATGGCGCTCGCGGGCCCT
CGGCATCGGCTCTTCGCGCTGCTGCCCAGCGACAACTCGCTGCTCACCAGCGTCTTCCCCGGCATGATCCTGCTCCTGCGGATGGCCACC
GGCCTGGTCGCATTGCAGAACGCCGCCCTGCACGCGGTCACCGAGGCCGACGCGGGCGTGGCCTCCGGCGTGCAACGCTGCGCCGACCAG
CTCGGCGGCGCGAGCGGTATCGCCGTCTACGTCAGCATCGGGTTCTCGCCCCACCTCGGCGGCGACTGGGACCCGTTCACCGTGGCGTAC
AGCCTCGCCGGCATCGGCCTGATCGCGGCCGTCCTCGCCGTCCTCGCCCTGTCTCCGGACCGCCGTCTCGCCGCCCCCCGGGAGCAGGAG
GACTGA