Nivala, Outi Faccio, Greta Arvas, Mikko Permi, Perttu Buchert, Johanna Kruus, Kristiina Mattinen, Maija-Liisa Additional file 5: of Characterization of sulfhydryl oxidase from Aspergillus tubingensis Details to Fig. 6 Candidate secondary metabolism clusters with SOX enzymes on fungal chromosomes. On the left an approximate phylogenetic tree of the species compiled from literature [54, 55]. On the right a stretch of a scaffold from each species containing the cluster and neighbouring genes. Genes are shown as boxes on the scaffold stretch. NRPS, PKS, P450 and Zn2 are indicated when present. Grey lines connect genes with identical protein domains on adjacent scaffolds (excluding NRPS, PKS, P450, Zn2 and SOX genes) in order to reveal syntenies. Codes above the gene boxes are their identifiers and below them the Interpro protein domain identifiers found in the genes. Panel a. shows the gliotoxin clusters, while panel b. shows other clusters. The strains shown in panel a. are Trichoderma reesei, Fusarium graminearum, Chaetomium globusum, Phaeosphaeria nodorum, A. tubingensis, A. oryzae and A. fumigatus. The stains shown in panel b. are F. graminearum, Magnaporthe grisea, A. fumigatus and Phanerochaete chrysosporium. (PNG 335 kb) Secreted sulfhydryl oxidase;Dithiol oxidase;Aspergillus tubingensis;Glutathione oxidation;Nonribosomal peptide synthesis;Secondary metabolism 2017-12-08
    https://springernature.figshare.com/articles/figure/Additional_file_5_of_Characterization_of_sulfhydryl_oxidase_from_Aspergillus_tubingensis/5683288
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