“…It can be divided into four domains. These are the N-terminal domain (P NTD, aa 1-90, RABV), which is disordered but adopts defined conformations upon interaction with N or L [37][38][39][40][41][42]; the central domain (P CED, aa 91-130, RABV); the C-terminal intrinsically disordered domain (P CID, aa 131-195, RABV); and the C-terminal domain (P CD, aa 195-296, RABV). The atomic structures of P CED (pdb: 2fqm [43], VSV; pdb: 3l32 [44], RABV), which mediates the dimerisation of the P-protein, and P CD (pdb: 2k47 [45], VSV; pdb: 1vyi [46], RABV), which is important for interacting with the N-RNA complex and parts of the VSV P NTD with N [37], have been resolved.…”