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. Author manuscript; available in PMC: 2024 Feb 1.
Published in final edited form as: Nat Chem Biol. 2022 Nov 28;19(2):218–229. doi: 10.1038/s41589-022-01202-4

Extended Data Fig. 1 |. Genomic organization of the predicted N-glycan utilization loci (N-GUL) from B. longum NCC2705.

Extended Data Fig. 1 |

a, Genes that compose N-GUL represented by arrows and their respective gene products. a = biochemically characterized in this work, b = predicted, c = characterized in previous works23,24,28. The symbol * represents transcriptional regulators (bl1336 – encoding a LacI transcriptional regulator and bl1340 – encoding a ROK transcriptional regulator). b, A schematic representation of a high-mannose N-glycan indicating its subunits (geometric forms), glycosidic linkages (gray symbols) and the cleavage sites (scissors) recognized by the GH5 β-mannosidase23 and GH85 ENGase24 enzymes previously characterized. Predictions of uncharacterized enzymes were performed by sequence and hidden-Markov similarities analyses (Supplementary Tables 1, 2). c, Representation of Man9GlcNAc. d, Representation of Man5GlcNAc.