Norine

• Type:
• Smiles: CSCC[C@@H](C(=O)N(C(=O)C(C(N(C(=O)[C@H](Cc1cccc(c1)O)N)C)C)N)/C=C\1/OC(C(C1)O)n1ccc(=O)[nH]c1=O)NC(=O)NC(C(=O)O)Cc1cccc(c1)O
  
  
• Graph inference:


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• Atomic structure:

vizualisation:

• Links between organisms producing the MRD A:

• Identification of a napsamycin biosynthesis gene cluster by genome mining.
  Chembiochem : a European journal of chemical biology , 2011, 12(3):477-87
  DOI: 10.1002/cbic.201000460
  pubMed: 21290549

• NRPS substrate promiscuity leads to more potent antitubercular sansanmycin analogues.
  Journal of natural products , 2014, 77(7):1744-8
  DOI: 10.1021/np5001494
  pubMed: 24964393

• Identification of a novel beta-replacement reaction in the biosynthesis of 2,3-diaminobutyric acid in peptidylnucleoside mureidomycin A.
  Organic & biomolecular chemistry , 2008, 6(11):1912-7
  DOI: 10.1039/b802585a
  pubMed: 18480903

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