Fig. 4From: Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family3D–Models. a Normal TCIRG1 b Mutant TCIRG1 (p.P208PfsX1). Docking complex visualization: c TCIRG1 vs ATPV1B1 d Mutant TCIRG1 vs ATPV1B1. Receptor protein has been shown in solid ribbon display style with green color; ligand has been shown in secondary type with yellow colorBack to article page