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capreomycin IA


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  • Norine ID: NOR00638
  • DOI: 10.26097/nor00638
  • Family: capreomycin
  • Synonym(s): capreomycin IA;
  • Activity: antimicrobial
  • Category: peptide
  • Formula: C25H44N14O8
  • Monoisotopic mass: 668.3466544539999 g/mol
  • Comment: The tuberactinomycin antibiotics are essential components in the drug arsenal against Mycobacterium tuberculosis infections and are specifically used for the treatment of multidrug-resistant tuberculosis.
  • Source: norine
  • Contributor (creation): Norine Team [CRIStAL (UMR CNRS 9189), ex-LIFL, France, Charles Viollette Institute, ProBioGEM team, Lille, France, University of Lille, France]
  • Entry information:
  • Type: partial cyclic
  • Number of monomers: 6
  • Smiles: NCCCC(N)CC(=O)NCC1NC(=O)C(CO)NC(=O)C(N)CNC(=O)C(NC(=O)C(=CNC(N)=O)NC1(=O))C2CCN=C(N)N2

  • Graph inference:



  • Monomeric composition and PDB SEQRES:
    1
    bLys
    1
    KBE
    2
    Dpr
    2
    DPP
    3
    bU-dAla
    3
    UAL
    4
    Cap
    4
    MYN
    5
    Dpr
    5
    DPP
    6
    Ser
    6
    SER
  • Graph representation: bLys,Dpr,bU-dAla,Cap,Dpr,Ser @1 @0,2,5 @1,3 @2,4 @3,5 @1,4

  • Atomic structure:
  • Chemical structure
    rBAN vizualisation:
  • Streptomyces
  • gram: positive
  • taxid: 68187 (view NCBI taxonomy browser)

  • Links between organisms producing the capreomycin IA: Streptomyces
  • Identification of the biosynthetic gene cluster and an additional gene for resistance to the antituberculosis drug capreomycin
    Thomas MG, Berti AD, Felnagle EA, Rondon MR, Crosby HA, Applied and environmental microbiology , 2007, Jul,73(13):4162-70. Epub 2007 May 11.
    DOI: 10.1128/AEM.00485-07
    pubMed: 17496129


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