AAC(3)-Ib

Accession ARO:3002530
Synonym(s)aacCA2
CARD Short NameAAC(3)-Ib
DefinitionAAC(3)-Ib is an integron-encoded aminoglycoside acetyltransferase in P. aeruginosa.
AMR Gene FamilyAAC(3)
Drug Classaminoglycoside antibiotic
Resistance Mechanismantibiotic inactivation
Resistomes with Perfect MatchesCitrobacter amalonaticuswgs, Enterobacter cloacaep+wgs, Enterobacter hormaecheip+wgs, Klebsiella michiganensisp+wgs, Klebsiella pneumoniaewgs, Klebsiella quasipneumoniaewgs, Pseudomonas aeruginosawgs, Serratia marcescenswgs
Resistomes with Sequence VariantsCitrobacter amalonaticuswgs, Citrobacter freundiiwgs, Enterobacter cloacaep+wgs, Enterobacter hormaecheip+wgs, Escherichia coligi, Klebsiella michiganensisp+wgs, Klebsiella pneumoniaewgs, Klebsiella quasipneumoniaewgs, Pseudomonas aeruginosawgs, Salmonella entericagi, Serratia marcescenswgs
Classification12 ontology terms | Show
Parent Term(s)4 ontology terms | Show
+ confers_resistance_to_antibiotic sisomicin [Antibiotic]
+ confers_resistance_to_antibiotic astromicin [Antibiotic]
+ AAC(3)-I
+ confers_resistance_to_antibiotic gentamicin [Antibiotic]
Publications

Schwocho LR, et al. 1995. Antimicrob Agents Chemother 39(8): 1790-1796. Cloning and characterization of a 3-N-aminoglycoside acetyltransferase gene, aac(3)-Ib, from Pseudomonas aeruginosa. (PMID 7486920)

Resistomes

Prevalence of AAC(3)-Ib 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
Citrobacter amalonaticus0%0%1.82%0%
Citrobacter freundii0%0%0.19%0%
Enterobacter cloacae0%0.56%0.64%0%
Enterobacter hormaechei0%0.45%0.47%0%
Escherichia coli0%0%0%0.13%
Klebsiella michiganensis0%1.71%0.8%0%
Klebsiella pneumoniae0%0%0.02%0%
Klebsiella quasipneumoniae0%0%0.26%0%
Pseudomonas aeruginosa0%0%0.13%0%
Salmonella enterica0%0%0%1.32%
Serratia marcescens0%0%0.13%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): 300


>gb|AAA88422.1|+|AAC(3)-Ib [Pseudomonas aeruginosa]
MLWSSNDVTQQGSRPKTKLGGSMSIIATVKIGPDEISAMRAVLDLFGKEFEDIPTYSDRQPTNEYLANLLHSETFIALAAFDRGTAIGGL
AAYVLPKFEQARSEIYIYDLAVASSHRRLGVATALISHLKRVAVELGAYVIYVQADYGDDPAVALYTKLGVREDVMHFDIDPRTAT


>gb|L06157.1|+|555-1085|AAC(3)-Ib [Pseudomonas aeruginosa]
ATGTTATGGAGCAGCAACGATGTTACGCAGCAGGGCAGTCGCCCTAAAACAAAGTTAGGTGGCTCAATGAGCATCATTGCAACCGTCAAG
ATCGGCCCTGACGAAATTTCAGCCATGAGGGCTGTGCTCGATCTCTTCGGCAAAGAGTTTGAGGACATTCCAACCTACTCTGATCGCCAG
CCGACCAATGAGTATCTTGCCAATCTTCTGCACAGCGAGACGTTCATCGCGCTCGCTGCTTTTGACCGCGGAACAGCAATAGGTGGGCTC
GCCGCCTACGTTCTACCCAAGTTCGAGCAAGCGCGAAGCGAGATCTACATTTATGACTTGGCAGTCGCTTCCAGCCATCGAAGGCTAGGA
GTCGCAACTGCCCTGATTAGCCACCTGAAGCGTGTGGCGGTTGAACTTGGCGCGTATGTAATCTATGTGCAAGCAGACTACGGTGACGAT
CCGGCAGTCGCTCTCTACACAAAGCTTGGAGTTCGGGAAGACGTCATGCACTTCGACATTGATCCAAGAACCGCCACCTAA