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Table 1 Summary of residues involved in WNT1 docking interactions (Wild & Mutant)

From: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

Receptor/Ligand

Hydrogen Bond Interactions

Hydrophobic Bond Interactions

Ligand Residues

Receptor Residues

Ligand Residues

Receptor Residues

Wild WNT1-Axin 1

Val383, Glu391, Arg395, Val399, Gln400

Arg98, Cys218, Arg344, Cys347, Cys352

Glu384, Pro385, Phe388, Ala389, Leu392, Leu396, Arg401

Arg215, Gln216, Glu217, Arg235, Thr238, Arg240, Asp244, Arg247, Pro320, Thr348, Phe349, His350, Val355

Mutated WNT1-Axin 1

Gln386, Phe388, Glu390, Leu396, Glu397, Gln400

Lys51, Trp95, Arg98, Arg337, Glu368

Val383, Glu391, Leu392, Val399

Asn29, Ser50, Arg91, Lys94, Gly312, Arg335