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. 2022 Aug 17;12:13928. doi: 10.1038/s41598-022-18348-9

Table 6.

Molecular docking scores for curcumin, CCA-1.1, and PGV-1 against wild-type and mutant EGFR.

Drug Protein Binding Energy (kcal/Mol) No of H bonds Interacting amino acids (Distance)
Curcumin EGFR (wild-type) −11.05 1 Gln684 (2.97)
EGFR (E709K) −11.74 3 Gly696 (2.21), Pro699 (3.08), Asn700 (3.44)
EGFR (T263P) −10.12 2 Arg686 (2.98), Glu736 (3.19)
EGFR (V774M) −11.94 2 Asn298 (1.84), Arg831 (2.13)
EGFR (L861Q) −10.51 2 Arg297 (1.92), Leu707 (3.00)
CCA-1.1 EGFR (wild-type) −12.51 2 Arg53 (1.80), Glu687 (1.79)
EGFR (E709K) −11.02 3 Val30 (2.04), Met54 (3.76), Arg297 (1.93)
EGFR (T263P) −11.29 1 Tyr299 (2.02)
EGFR (V774M) −10.91 1 Val30 (2.09)
EGFR (L861Q) −12.62 1 Val689 (3.13)
PGV-1 EGFR (wild-type) −13.87 1 Arg686 (1.84)
EGFR (E709K) −10.73 1 Leu777 (2.29)
EGFR (T263P) −10.37
EGFR (V774M) −10.58 1 Leu861 (3.09)
EGFR (L861Q) −11.82 2 Phe723 (2.12), Lys875 (2.85)