Clostridium perfringes cplR

Accession ARO:3007644
CARD Short NameCper_cplR
DefinitionCplR is an ABC-F ATPase ribosomal protection protein from Clostridium perfringes which confers resistance to pleuromutilins and lincosamides.
AMR Gene FamilyMiscellaneous ABC-F subfamily ATP-binding cassette ribosomal protection proteins
Drug Classstreptogramin antibiotic, pleuromutilin antibiotic, streptogramin A antibiotic, lincosamide antibiotic
Resistance Mechanismantibiotic target protection
Classification11 ontology terms | Show
Parent Term(s)6 ontology terms | Show
+ confers_resistance_to_antibiotic lincomycin [Antibiotic]
+ confers_resistance_to_antibiotic clindamycin [Antibiotic]
+ confers_resistance_to_antibiotic virginiamycin M1 [Antibiotic]
+ confers_resistance_to_antibiotic retapamulin [Antibiotic]
+ Miscellaneous ABC-F subfamily ATP-binding cassette ribosomal protection proteins [AMR Gene Family]
+ confers_resistance_to_antibiotic iboxamycin [Antibiotic]
Publications

Obana N, et al. 2023. Nucleic Acids Res 51(9):4536-4554 Genome-encoded ABCF factors implicated in intrinsic antibiotic resistance in Gram-positive bacteria: VmlR2, Ard1 and CplR. (PMID 36951104)

Resistomes

Prevalence of Clostridium perfringes cplR 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

SpeciesNCBI ChromosomeNCBI PlasmidNCBI WGSNCBI GI
No prevalence data


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): 950


>gb|BAB80490.1|-|Clostridium perfringes cplR [Clostridium perfringens str. 13]
MTFYDYIYSPVIYRRDFFMSLARLNKVKKYYGDKLILDIDKLEILDEDRIGLVGVNGAGKTTLIKSLLGQIPIDEGNVSLTKSFAYISQS
ENSNEETLNNNFKNVFNAPFEYHEFLSGGEKVKFKIAKALGENKHLIIADEPTANLDENSIETLENMLKNYNGALLLVSHDRRFLDSLCN
TIIEIEDGKIKTYKGNFSKYLELKTLERQRAEIEYNSYINEKKHLENAILNKRNLKDSLRKTPKRMGNSEARLHKMGPQRAKKNLDNNIK
ALRSRIDHLDIKEKPKTIKEIKIRVQDNLKIASKNLIEAKDFTLFAGNKLLLKDIKFKIKNGKKVALIGDNGCGKSTLLKNIISKEDNIK
VLDNVVIGYFDQSQKILKDDESILKNILKDCSYDENFVRINLDGFGFKGDDVFKKVSSLSGGEKVKIALCKILLSDNNLIILDEPTNYLD
IKSMESLETALINCNKTLIVVSHDRNFISNVCDYILEIDNNLIHEFSGTYDEYIKFKKKPKLDDKERANKDSLLLLENRLSNVISLLSIE
PDNNKKSLLENEYYNLLKELKNLRKRLS


>gb|BA000016.3|-|967229-968935|Clostridium perfringes cplR [Clostridium perfringens str. 13]
TTGACTTTTTATGACTATATATACTCTCCTGTAATTTATAGGAGGGATTTTTTTATGTCTTTAGCAAGATTAAATAAAGTAAAAAAATAT
TATGGAGATAAATTAATTCTAGATATAGATAAACTAGAAATTTTAGATGAAGATAGAATCGGATTAGTTGGAGTTAATGGTGCTGGTAAA
ACTACACTTATTAAATCTTTATTAGGTCAAATTCCTATTGATGAAGGAAATGTATCTCTAACTAAAAGCTTTGCTTATATAAGTCAAAGT
GAAAATTCTAATGAAGAAACTTTAAATAATAATTTTAAGAATGTATTCAATGCTCCTTTTGAATACCATGAGTTTTTATCAGGTGGAGAA
AAGGTTAAATTTAAAATAGCTAAAGCTCTAGGTGAAAATAAACATTTAATTATTGCTGATGAGCCTACTGCTAATTTAGATGAAAACAGC
ATTGAAACTCTTGAAAACATGCTAAAAAACTATAATGGTGCATTACTTCTAGTATCACATGATAGAAGATTTCTAGATTCATTATGTAAC
ACTATTATTGAAATTGAAGATGGAAAAATAAAAACTTATAAAGGAAATTTCTCTAAATATCTAGAGCTAAAAACTTTAGAGAGGCAAAGA
GCTGAAATTGAGTATAATTCTTATATAAATGAAAAAAAGCATCTTGAAAATGCTATCCTTAATAAGCGAAACTTAAAAGATAGTCTTCGA
AAAACACCTAAAAGAATGGGTAATTCTGAAGCTAGATTACACAAAATGGGGCCTCAAAGAGCAAAGAAAAATCTAGATAATAATATAAAG
GCCTTAAGAAGTAGAATTGATCATCTTGACATTAAGGAAAAGCCTAAAACAATAAAAGAGATTAAAATTAGAGTTCAAGATAATTTAAAA
ATAGCTTCTAAAAATCTTATAGAAGCTAAAGATTTCACATTATTTGCAGGTAATAAGCTTCTACTTAAAGATATTAAATTTAAAATAAAG
AATGGTAAGAAAGTAGCACTTATTGGTGATAATGGTTGTGGTAAAAGTACATTGCTAAAAAATATTATTTCAAAAGAAGACAATATAAAA
GTTTTAGATAATGTTGTTATAGGCTACTTTGATCAATCTCAAAAGATATTAAAAGATGATGAATCAATACTAAAAAATATTCTTAAAGAT
TGTTCTTATGATGAAAATTTTGTGAGAATAAATCTAGATGGTTTTGGTTTTAAAGGAGATGATGTATTTAAGAAAGTCTCTTCCTTAAGT
GGTGGTGAAAAAGTAAAAATAGCACTTTGTAAAATATTATTATCTGATAATAACTTAATAATATTGGACGAACCTACAAACTATCTTGAC
ATAAAATCTATGGAATCTCTAGAGACTGCATTGATTAATTGTAATAAAACATTAATTGTAGTTTCTCATGATAGAAACTTTATTTCTAAT
GTATGCGATTATATTTTAGAGATAGATAACAATTTAATTCATGAATTTTCTGGCACCTATGATGAATATATAAAATTTAAGAAAAAACCT
AAGTTAGATGATAAAGAAAGAGCTAATAAAGATAGTCTTCTTCTCTTAGAAAACAGACTTTCTAATGTAATATCGCTCCTTTCAATAGAA
CCTGACAACAATAAAAAAAGTTTATTAGAAAATGAATATTATAATTTACTTAAAGAATTAAAAAACTTAAGAAAAAGATTAAGTTAA