Fig. 5From: HT-SIP: a semi-automated stable isotope probing pipeline identifies cross-kingdom interactions in the hyphosphere of arbuscular mycorrhizal fungiGenomic comparison of Myxococcota MAGs versus Myxococcota type species for CAZyme gene content and genome characteristics. Heatmap rows indicate the number of gene homologs (red-blue color scale) detected per CAZy family, and columns indicate the associated MAGs. Atom percent excess 13C (APE-13C) estimated by qSIP is presented in the top row (yellow-purple-black color scale). Columns and rows were grouped using one-dimensional hierarchical clustering based on genomic content. CAZy families displayed had significantly more or less genes detected in the Fen-1088 MAGs compared to the rest of our Myxococcota MAGs (Student’s t test, p <0.05); full CAZy results for the MAGs are available in Supplemental Table S6. Bar graphs indicate genome %GC content and genome size (Mbp), as well as number of protease, glycoside hydrolase, and polysaccharide lyase gene homologs per genome. The type species (Labilithrix luteola, Anaeromyxobacter dehalogenans 2CP-1, Nannocystis exedens, Haliangium ochraceum DSM 14365, Myxococcus xanthus, Archangium gephyra, Sorangium cellulosum B) were clustered with our MAGs and 25 other Myxococcota type species (Supplemental Figure S3); a single type species genome was selected the represent each cluster for this figure. Acronyms: GH = glycoside hydrolase; PL = polysaccharide lyase; CBM = carbohydrate binding module; GT = glycosyltransferase; AA = auxiliary activityBack to article page