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Jagaricin


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  • Norine ID: NOR01984
  • DOI:
  • Family: jagaricin
  • Synonym(s):
  • Activity: antimicrobial
  • Class: lipopeptide
  • Formula: C56H84N12O16
  • Monoisotopic mass: 1180.6128247000001 g/mol
  • Source: mynorine
  • Contributor (creation): Matthieu Duban [UMR BioEcoAgro 1158 ICV]
  • Entry information:
  • Type: partial cyclic
  • Number of monomers: 10
  • Smiles: CCCCCCCCCCC[C@@H](CC(=O)N/C(=C\C)/C(=O)N[C@H]1[C@H](OC(=O)[C@H](NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](NC(=O)/C(=C\C)/NC(=O)[C@H](NC(=O)[C@H](NC1=O)[C@H](C)O)CC2=CC=C(C=C2)O)CCC(=O)N)[C@H](C)O)CC3=CN=CN3)C)O

  • Graph inference:



  • Monomeric composition :
    1
    Gly
    2
    Tyr
    3
    dhAbu
    4
    Thr
    5
    Thr
    6
    C14:0-OH(3)
    7
    dhAbu
    8
    Gln
    9
    Thr
    10
    His
  • Graph representation: Gly,Tyr,dhAbu,Thr,Thr,C14:0-OH(3),dhAbu,Gln,Thr,His @4,7 @6,3 @5,8 @1,8 @0,9 @2 @1,7 @0,6 @2,3,9 @4,8

  • Atomic structure:
  • Chemical structure
    rBAN vizualisation:
  • Janthinobacterium agaricidamnosum
  • gram: negative
  • taxid: 1349767 (view NCBI taxonomy browser)

  • Links between organisms producing the Jagaricin: Janthinobacterium agaricidamnosum
  • Imaging mass spectrometry and genome mining reveal highly antifungal virulence factor of mushroom soft rot pathogen
    Katharina Graupner, Kirstin Scherlach, Tom Bretschneider, Gerald Lackner, Martin Roth, Harald Gross, Christian Hertweck, Angew Chem Int Ed Engl . , 2012, 51(52):13173-7
    DOI: 10.1002/anie.201206658
    pubMed: 23161559


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