EreA

Accession ARO:3000361
Synonym(s)Ere(A)
CARD Short NameEreA
DefinitionEreA is an erythromycin esterase that hydrolyses the drug's lactone ring.
AMR Gene Familymacrolide esterase
Drug Classmacrolide antibiotic
Resistance Mechanismantibiotic inactivation
Resistomes with Perfect MatchesEnterobacter hormaecheiwgs, Klebsiella pneumoniaewgs, Pseudomonas aeruginosawgs, Pseudomonas putidawgs
Resistomes with Sequence VariantsActinobacillus pleuropneumoniaeg, Aliarcobacter butzleriwgs, Citrobacter freundiiwgs, Enterobacter cloacaewgs, Enterobacter hormaecheip+wgs, Escherichia colig+wgs, Klebsiella pneumoniaeg+wgs+gi, Klebsiella quasipneumoniaewgs, Laribacter hongkongensisg+wgs+gi, Proteus mirabilisg+wgs+gi, Pseudomonas aeruginosag+wgs, Pseudomonas putidag+wgs, Salmonella entericawgs, Serratia marcescensp, Vibrio alginolyticusg, Vibrio parahaemolyticuswgs
Classification10 ontology terms | Show
Parent Term(s)4 ontology terms | Show
+ confers_resistance_to_antibiotic erythromycin [Antibiotic]
+ confers_resistance_to_antibiotic roxithromycin [Antibiotic]
+ confers_resistance_to_antibiotic clarithromycin [Antibiotic]
+ macrolide esterase [AMR Gene Family]
Publications

Morar M, et al. 2012. Biochemistry 51(8): 1740-1751. Mechanism and diversity of the erythromycin esterase family of enzymes. (PMID 22303981)

Resistomes

Prevalence of EreA 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
Actinobacillus pleuropneumoniae2.78%0%0%0%
Aliarcobacter butzleri0%0%0.81%0%
Citrobacter freundii0%0%0.77%0%
Enterobacter cloacae0%0%0.32%0%
Enterobacter hormaechei0%0.06%0.13%0%
Escherichia coli0.05%0%0.03%0%
Klebsiella pneumoniae0.06%0%0.08%0.95%
Klebsiella quasipneumoniae0%0%0.13%0%
Laribacter hongkongensis66.67%0%2.08%50%
Proteus mirabilis19.27%0%3.96%18.52%
Pseudomonas aeruginosa0.15%0%0.09%0%
Pseudomonas putida1.41%0%0.53%0%
Salmonella enterica0%0%0.02%0%
Serratia marcescens0%0.65%0%0%
Vibrio alginolyticus1.23%0%0%0%
Vibrio parahaemolyticus0%0%0.05%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): 650


>gb|AAO38247.1|+|EreA [Escherichia coli]
MTWRTTRTLLQPQKLDFNEFEILTSVIEGARIVGIGEGAHFVAEFSLARASLIRYLVERHEFNAIGLECGAIQASRLSEWLNSTAGAHEL
ERFSDTLTFSVYGSVLIWLKSYLRESGRKLQLVGIDLPNTLNPRDDLAQLAEIIQLIDHLMKPHVDMLTHLLASIDGQSAVISSAKWGEL
ETARQEKAISGVTRLKLRLASLAPVLKKHVNSDLFRKASDRIESIEYTLETLRIMKTFFDGTSLEGDTSVRDSYMAGVVDGMVRANPDVK
IILLAHNNHLQKTPVSFSGELTAVPMGQHLAERVNYRAIAFTHLGPTVPEMHFPSPKSPLGFSVVTTPADAIREDSMEQYVIDACGTENS
CLTLTDAPMEAKRMRSQSASVETKLSEAFDAIVCVTSAGKDSLVAL


>gb|AY183453.1|+|2730-3950|EreA [Escherichia coli]
ATGACATGGAGAACGACCAGAACACTTTTACAGCCTCAAAAGCTGGACTTCAATGAGTTTGAGATTCTTACTTCCGTAATTGAGGGCGCC
CGAATTGTCGGCATTGGCGAGGGCGCTCATTTTGTCGCGGAGTTTTCACTGGCTAGAGCTAGTCTTATCCGCTATTTGGTCGAAAGGCAT
GAGTTTAATGCGATTGGTTTGGAATGTGGGGCGATTCAGGCATCCCGGTTATCTGAATGGCTCAACTCAACAGCCGGTGCTCATGAACTT
GAGCGATTTTCGGATACCCTGACCTTTTCTGTGTATGGCTCAGTGCTGATCTGGCTGAAATCATATCTCCGCGAATCAGGAAGAAAACTG
CAGTTAGTCGGAATCGACTTACCCAACACCCTGAACCCAAGGGACGACCTAGCGCAATTGGCCGAAATTATCCAGCTCATCGATCACCTC
ATGAAACCGCACGTTGATATGTTGACTCACTTGTTGGCGTCCATTGATGGCCAGTCGGCGGTTATTTCATCGGCAAAATGGGGGGAGCTA
GAAACGGCTCGGCAGGAGAAAGCTATCTCAGGGGTAACCAGATTGAAGCTCCGCTTGGCGTCGCTTGCCCCCGTCCTGAAAAAACACGTC
AACAGCGATTTGTTCCGAAAAGCCTCTGATCGAATAGAGTCGATAGAGTATACGTTGGAAACCTTGCGTATAATGAAAACTTTCTTCGAT
GGTACCTCTCTTGAGGGAGATACTTCCGTACGTGACTCGTATATGGCGGGCGTAGTAGATGGAATGGTTCGAGCGAATCCGGATGTGAAG
ATAATTCTGCTGGCGCACAACAATCATCTACAAAAAACTCCAGTCTCCTTTTCAGGCGAGCTTACGGCTGTTCCCATGGGGCAGCACCTC
GCAGAGAGGGTGAATTACCGTGCGATTGCATTCACCCATCTTGGACCCACCGTGCCGGAAATGCATTTCCCATCGCCAAAAAGTCCTCTT
GGATTCTCTGTTGTGACCACGCCTGCCGATGCAATCCGTGAGGATAGTATGGAACAGTATGTCATCGACGCCTGTGGTACGGAGAATTCA
TGTCTGACATTGACAGATGCCCCCATGGAAGCAAAGCGAATGCGGTCTCAAAGCGCCTCTGTAGAAACGAAATTGAGCGAGGCATTTGAT
GCCATCGTCTGTGTTACAAGCGCCGGCAAGGACAGCCTGGTTGCCCTATAG