Mycobacterium tuberculosis fbiB with mutation conferring resistance to delamanid

Ontology CARD's Antibiotic Resistance Ontology
Accession ARO:3009340
CARD Short NameMtub_fbiB_DLM
DefinitionfbiB is an enzyme in the Coenzyme F420 biosynthesis pathway of Mycobacterium tuberculosis. Mutations in fbiB are associated with increased resistance to the antibiotic delamanid.
AMR Gene Familyantibiotic resistant F420 biosynthesis protein
Drug Classnitroimidazole antibiotic
Resistance Mechanismantibiotic target alteration
Classification8 ontology terms | Show
Parent Term(s)2 ontology terms | Show
+ confers_resistance_to_antibiotic delamanid [Antibiotic]
+ antibiotic resistant F420 biosynthesis protein [AMR Gene Family]
Publications

World Health Organization. 2023. ISBN 978-92-4-008241-0. Catalogue of mutations in Mycobacterium tuberculosis complex and their association with drug resistance. Second Edition. (ISBN 978-92-4-008241-0)

Resistomes

Prevalence of Mycobacterium tuberculosis fbiB with mutation conferring resistance to delamanid among the sequenced genomes, plasmids, and whole-genome shotgun assemblies available at NCBI or IslandViewer for 414 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 GIGRDI-AMR2
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): 800


>gb|NP_217779.1|+|Mycobacterium tuberculosis fbiB with mutation conferring resistance to delamanid [Mycobacterium tuberculosis H37Rv]
MTGPEHGSASTIEILPVIGLPEFRPGDDLSAAVAAAAPWLRDGDVVVVTSKVVSKCEGRLVPAPEDPEQRDRLRRKLIEDEAVRVLARKD
RTLITENRLGLVQAAAGVDGSNVGRSELALLPVDPDASAATLRAGLRERLGVTVAVVITDTMGRAWRNGQTDAAVGAAGLAVLRNYAGVR
DPYGNELVVTEVAVADEIAAAADLVKGKLTATPVAVVRGFGVSDDGSTARQLLRPGANDLFWLGTAEALELGRQQAQLLRRSVRRFSTDP
VPGDLVEAAVAEALTAPAPHHTRPTRFVWLQTPAIRARLLDRMKDKWRSDLTSDGLPADAIERRVARGQILYDAPEVVIPMLVPDGAHSY
PDAARTDAEHTMFTVAVGAAVQALLVALAVRGLGSCWIGSTIFAADLVRDELDLPVDWEPLGAIAIGYADEPSGLRDPVPAADLLILK


>gb|NC_000962.3|+|3641535-3642881|Mycobacterium tuberculosis fbiB with mutation conferring resistance to delamanid [Mycobacterium tuberculosis H37Rv]
TTGACCGGCCCCGAACATGGCTCCGCCTCGACCATCGAGATCCTGCCCGTCATCGGGCTGCCCGAATTCCGTCCCGGCGACGATCTGAGC
GCCGCCGTCGCCGCGGCGGCACCGTGGCTACGCGACGGTGACGTCGTGGTGGTTACCAGCAAGGTGGTGTCCAAATGCGAGGGCCGGCTG
GTTCCGGCTCCCGAAGACCCCGAGCAAAGAGACCGATTGCGCCGCAAGCTGATCGAGGATGAGGCAGTGCGCGTGTTGGCGCGCAAGGAC
CGCACGTTGATCACCGAGAATCGACTCGGGCTGGTTCAGGCGGCCGCCGGCGTGGACGGATCCAACGTCGGCCGGTCCGAGTTAGCGCTG
CTGCCGGTCGATCCTGACGCCAGTGCCGCAACCTTGCGCGCCGGGCTGCGCGAGCGGCTCGGCGTCACCGTCGCCGTGGTCATCACCGAC
ACCATGGGACGCGCCTGGCGCAACGGCCAGACCGATGCCGCAGTCGGCGCTGCCGGTCTGGCGGTGCTGCGCAACTATGCCGGTGTCCGC
GACCCATACGGCAATGAGTTGGTGGTCACCGAGGTCGCAGTCGCCGACGAGATCGCCGCGGCCGCCGACTTGGTCAAAGGCAAACTGACC
GCGACGCCGGTGGCGGTGGTGCGTGGGTTCGGCGTGTCCGACGACGGCTCGACAGCCCGGCAACTGCTGCGGCCGGGCGCCAACGACCTG
TTCTGGCTCGGGACCGCCGAAGCGCTCGAGCTGGGTCGCCAGCAAGCCCAACTGTTGCGCAGGTCCGTTCGCCGGTTTAGCACCGATCCG
GTGCCGGGCGACCTCGTCGAGGCTGCGGTCGCCGAGGCCCTCACCGCGCCAGCCCCACATCACACCCGGCCGACCCGATTCGTGTGGCTG
CAGACACCGGCCATCCGCGCGCGGCTGCTAGATCGGATGAAAGACAAGTGGCGGTCTGATCTCACCAGTGACGGCTTGCCCGCCGACGCG
ATAGAACGCCGGGTGGCACGCGGCCAGATCCTCTATGACGCACCCGAAGTCGTCATACCGATGCTGGTGCCCGACGGAGCACACAGCTAC
CCCGATGCCGCCCGCACCGACGCCGAGCACACCATGTTCACGGTCGCCGTCGGAGCGGCCGTACAAGCCTTGCTGGTCGCGCTGGCCGTG
CGCGGGCTGGGCAGTTGCTGGATCGGCTCGACGATCTTTGCCGCTGACCTGGTCCGCGACGAGCTGGACCTGCCAGTCGACTGGGAGCCG
TTGGGCGCCATCGCGATCGGATATGCCGACGAGCCGTCCGGGTTGCGCGACCCGGTGCCTGCCGCCGATTTGCTGATCCTGAAGTGA

Curator Acknowledgements
Curator Description Most Recent Edit