2C1E
crystal structures of caspase-3 in complex with aza-peptide michael acceptor inhibitors.
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains A-B
Int. Res. 168
Norm. En. per Res. -5.5412
Hub Node A(2)
Click on the Nodes or Edges in the network to see the details
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 -190.7404 -16.3146 -723.869 -930.924 168 37 14 25122 1 42 35
A-C 0.0 -7.3357 -12.2729 -19.6086 19 0 0 519 0 5 4
B-C -34.7048 -32.7437 -75.3432 -142.7918 27 4 1 2626 2 9 7