3GJT
caspase-3 binds diverse p4 residues in peptides
Total interactions analyzed 15
Total true interactions 10
Strongest Interaction Chains B-E
Int. Res. 33
Norm. En. per Res. -5.6793
Hub Node A(4)
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Weak Strong
Width of edge <-> No. of inter. res.
All Interactions
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Chains Hydro. Bond Ener. (kJ/mol) Elec. Ener. (kJ/mol) VDW. Ener. (kJ/mol) Tot. Stab. Ener. (kJ/mol) #int. res. # Short cont. #Hydr. int. #VDW pairs #salt bridges #Pot. fav. elec. int #Pot. unfav. elec. int int. res.
A-B -170.3655 -5.1432 -682.175 -857.6837 167 28 14 24250 2 37 28
A-C 0.0 -2.0069 -51.7859 -53.7927 40 2 0 2326 0 22 13
A-D -52.1833 6.8628 -97.8363 -143.1568 39 13 2 3527 0 12 10
A-E -29.1836 -31.6275 -28.9243 -89.7354 28 13 0 1223 2 7 8
B-C -31.1728 14.4423 -93.1784 -109.9089 39 6 2 3267 0 5 11
B-D -81.3378 -104.3333 -422.622 -608.2931 111 16 7 16202 7 42 33
B-E -44.6551 -47.5023 -95.2585 -187.4158 33 8 2 3649 2 7 4
C-D -164.2432 -11.8932 -692.955 -869.0914 167 39 14 24301 2 39 29
C-F -25.3071 -30.3427 -24.1045 -79.7543 28 15 0 1189 2 7 8
D-F -38.5517 -48.2785 -99.3396 -186.1698 33 8 2 3747 2 7 4