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. 2021 Mar 26;16(3):e0249324. doi: 10.1371/journal.pone.0249324

Fig 2. Swissmodel predicted 3-dimensional (3D) structure for human NRXN2 with mutation p.G849D (p.G889D) in complex with N-acetyl-D-glucosamine (NAG).

Fig 2

Each domain is colour coded, EGF-like domains are labelled B and C, substrate NAG are labelled as well as the mutation, p.G889D in our protein model.