TxR

Accession ARO:3005008
CARD Short NameTxR
DefinitionTxR is a putative transcription regulator that plays a role in conferring tetracycline resistance. It is required for proper functioning of Tet35.
AMR Gene FamilyATP-binding cassette (ABC) antibiotic efflux pump
Drug Classtetracycline antibiotic
Resistance Mechanismantibiotic efflux
Efflux Componentefflux pump complex or subunit conferring antibiotic resistance
Efflux Regulatorprotein(s) and two-component regulatory system modulating antibiotic efflux
Resistomes with Sequence VariantsVibrio alginolyticusg+wgs, Vibrio fluvialisg+wgs, Vibrio harveyig+wgs, Vibrio neocaledonicusg, Vibrio owensiiwgs, Vibrio parahaemolyticusg+wgs
Classification10 ontology terms | Show
Parent Term(s)2 ontology terms | Show
Publications

Teo JW, et al. 2002. Antimicrob Agents Chemother 46(4): 1038-1045. Genetic determinants of tetracycline resistance in Vibrio harveyi. (PMID 11897587)

Resistomes

Prevalence of TxR 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 homolog model (view sequences)

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GI
Vibrio alginolyticus6.17%0%9.13%0%
Vibrio fluvialis47.37%0%30.67%0%
Vibrio harveyi7.14%0%36%0%
Vibrio neocaledonicus50%0%0%0%
Vibrio owensii0%0%15.79%0%
Vibrio parahaemolyticus50%0%74.09%0%
Show Perfect Only


Detection Models

Model Type: protein homolog model

Model Definition: Protein Homolog Models (PHM) detect protein sequences based on their similarity to a curated reference sequence, using curated BLASTP bitscore cut-offs. Protein Homolog Models apply to all genes that confer resistance through their presence in an organism, such as the presence of a beta-lactamase gene on a plasmid. PHMs include a reference sequence and a bitscore cut-off for detection using BLASTP. A Perfect RGI match is 100% identical to the reference protein sequence along its entire length, a Strict RGI match is not identical but the bit-score of the matched sequence is greater than the curated BLASTP bit-score cutoff, Loose RGI matches have a bit-score less than the curated BLASTP bit-score cut-off.

Bit-score Cut-off (blastP): 400


>gb|AAK37618.1|+|TxR [Vibrio harveyi]
MKVQKCKATIHRRSLDADPLLPLIGNSTCISELRNKLKKYAQCDAEVLIQGETGVGKGMCARIIHELSSRHIYPFVEVNCGAIPSGLIAS
ELFGHEKGAFTGAISDRIGFIQKANKGTLFLDEIGDMPPDLQIHLLHFLESKQIHKVGADKIIDVDCRVIAASHVDLKSEVIQGGFREDL
FYRQNILPLTIPPLRKRGEDTVILSERFLEELSNGKVQSMSPEVKKKLLKHKWPGNVRELRNVIQRAIVMCEDNTLHIADLGLDNNERQL
LPSVEQIDLDYLLKAIEDNKHNMSAAARNLGISRTTLYRLIKKYNLPI


>gb|AF353562.1|+|964-1920|TxR [Vibrio harveyi]
ATGAAAGTGCAAAAATGCAAAGCTACGATACACAGACGTTCTTTGGATGCAGACCCATTACTTCCTCTTATTGGTAATAGCACTTGCATC
AGTGAACTACGTAACAAACTCAAAAAATACGCGCAATGTGATGCGGAAGTACTCATCCAAGGCGAAACCGGGGTGGGCAAAGGTATGTGT
GCTCGAATCATTCACGAACTTTCAAGTAGACATATATACCCATTTGTTGAAGTTAACTGCGGAGCGATTCCAAGCGGACTCATCGCATCA
GAGCTCTTCGGTCATGAGAAAGGAGCATTTACGGGGGCGATTTCGGATCGAATCGGCTTCATTCAAAAAGCGAACAAAGGGACGCTATTT
CTCGATGAAATCGGCGACATGCCGCCTGATCTACAAATTCATTTGCTGCATTTTTTGGAGAGTAAGCAAATCCATAAAGTTGGTGCAGAC
AAAATCATTGATGTGGATTGCCGCGTCATCGCAGCCAGCCATGTAGATTTAAAAAGTGAAGTAATACAAGGAGGATTCCGAGAGGATTTA
TTTTACCGACAAAACATACTACCACTCACTATCCCCCCACTTCGAAAGCGTGGTGAGGATACGGTCATATTGTCAGAGCGTTTTTTAGAA
GAATTATCCAACGGAAAAGTTCAGAGTATGTCTCCGGAAGTGAAGAAAAAGCTACTGAAACATAAATGGCCCGGCAACGTGAGAGAGCTG
CGCAATGTCATTCAAAGGGCGATTGTAATGTGTGAGGATAACACTCTTCACATCGCCGATCTCGGCTTGGACAATAACGAAAGACAGCTC
CTTCCCTCTGTTGAACAAATTGACTTAGATTATTTGTTAAAAGCAATCGAAGACAACAAACACAACATGAGTGCGGCTGCGAGGAATTTA
GGTATTTCTAGAACCACACTCTACCGTCTAATCAAGAAATATAACCTGCCCATCTAA