1MCF
principles and pitfalls in designing site directed peptide ligands
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains A-P
Int. Res. 17
Norm. En. per Res. -1.3112
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 -40.0012 15.0199 396.784 371.8026 198 49 15 17164 0 28 24
A-P 0.0 0.0 -22.2903 -22.2903 17 2 0 943 0 0 0
B-P 0.0 0.0 -15.3775 -15.3775 15 0 0 546 0 0 0