Characterisation of the ArmA adenylation domain implies a more diverse secondary metabolism in the genus Armillaria

Fungal Biology

Volumn 115, Issue 8, 2011, Pages 775-781

  Misiek, Mathias ^a   Braesel, Jana ^a   Hoffmeister, Dirk ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

Armillaria; Halogenase; Natural product; Nonribosomal peptide synthetase; Quinone synthetase; Secondary metabolism

Indexed keywords

AMINO ACID; FUNGAL PROTEIN; PEPTIDE SYNTHASE;

ALGORITHM; AMINO ACID; BIOCHEMICAL COMPOSITION; ENZYME ACTIVITY; FUNGUS; GENE EXPRESSION; GENOME; METABOLISM; MOLECULAR ANALYSIS; PEPTIDE; SECONDARY METABOLITE; SUBSTRATE;

AMINO ACID SEQUENCE; ARMILLARIA; ARTICLE; CHEMISTRY; CLASSIFICATION; ENZYME SPECIFICITY; ENZYMOLOGY; GENETICS; METABOLISM; MOLECULAR GENETICS; PHYLOGENY; PROTEIN TERTIARY STRUCTURE;

AMINO ACID SEQUENCE; AMINO ACIDS; ARMILLARIA; FUNGAL PROTEINS; MOLECULAR SEQUENCE DATA; PEPTIDE SYNTHASES; PHYLOGENY; PROTEIN STRUCTURE, TERTIARY; SUBSTRATE SPECIFICITY;

ARMA; ARMILLARIA; ARMILLARIA MELLEA; BASIDIOMYCOTA;

EID: 79960739048     PISSN: 18786146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.funbio.2011.06.002     Document Type: Article

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