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1.
Fig 4

Fig 4. Venn diagram showing number of unique and shared proteins experimentally identified in Ascomycete fungi secretomes.. From: Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.

Proteins identified via LC-MS/MS over a 21-day study. Total number of proteins identified for each fungus is indicated outside of diagram. Diagram generated with Venny 2.0 [Oliveros, J.C. (2007–2015) Venny. An interactive tool for comparing lists with Venn’s diagrams. http://bioinfogp.cnb.csic.es/tools/venny/index.html].

Carolyn A. Zeiner, et al. PLoS One. 2016;11(7):e0157844.
2.
Fig 5

Fig 5. Distribution of unique proteins experimentally identified in secretomes of four Ascomycete fungi.. From: Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.

(A) Proteins unique to each fungus based on amino acid sequence (as determined by JGI protein ID). (B) Proteins unique to each fungus based on predicted function (evaluated manually). Proteins identified via LC-MS/MS over a 21-day study. Total number of unique proteins identified for each fungus is indicated in center of circles. Abbreviations as in .

Carolyn A. Zeiner, et al. PLoS One. 2016;11(7):e0157844.
3.
Fig 2

Fig 2. Distribution of proteins experimentally identified in secretomes of four Ascomycete fungi among protein families.. From: Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.

Glycoside hydrolase families (both top and bottom panels). Solid bars: Portion of experimental secretome predicted to be secreted based on genome analysis. Shaded bars: Portion not predicted to be secreted. Proteins identified via LC-MS/MS over a 21-day study and classified according to the CAZy database. Abbreviations as in .

Carolyn A. Zeiner, et al. PLoS One. 2016;11(7):e0157844.
4.
Fig 3

Fig 3. Distribution of proteins experimentally identified in secretomes of four Ascomycete fungi among protein families.. From: Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.

(A, B) MEROPS peptidase families. (C) CAZy auxiliary activity families. (D) Other CAZyme families. Solid bars: Portion of experimental secretome predicted to be secreted based on genome analysis. Shaded bars: Portion not predicted to be secreted. Proteins identified via LC-MS/MS over a 21-day study and classified according to the CAZy and MEROPS databases. Abbreviations as in .

Carolyn A. Zeiner, et al. PLoS One. 2016;11(7):e0157844.
5.
Fig 6

Fig 6. Proteins unique to each genome among four Ascomycete fungi.. From: Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.

Genome analysis based on OrthoMCL (see text for details). Data are solely based on genomes and do not include experimental data. Solid bars: unique proteins predicted to be secreted. Shaded bars: unique proteins not predicted to be secreted. Colors as in Figs and . Total number of predicted proteins in each genome (including unique and non-unique): 13,469 (A. alternata); 14,745 (P. sporulosum); 14,995 (Pyrenochaeta sp.); 14,430 (Stagonospora sp.).

Carolyn A. Zeiner, et al. PLoS One. 2016;11(7):e0157844.
6.
Fig 1

Fig 1. Distribution of proteins identified in secretomes of four Ascomycete fungi among broad functional groups.. From: Comparative Analysis of Secretome Profiles of Manganese(II)-Oxidizing Ascomycete Fungi.

(A) Experimentally observed secretome. Proteins identified via LC-MS/MS over a 21-day study. (B) Portion of experimental secretome predicted to be secreted based on genome analysis (see text for further explanation). (C) Full predicted secretome based on genomes only. Total number of proteins identified for each fungus is indicated in center of circles. Abbreviations from CAZy database: AA = auxiliary activities; CBM = carbohydrate-binding module; CE = carbohydrate esterase; GH = glycoside hydrolase; GT = glucosyltransferase; PL = polysaccharide lyase.

Carolyn A. Zeiner, et al. PLoS One. 2016;11(7):e0157844.

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