1MCH
principles and pitfalls in designing site directed peptide ligands
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains A-P
Int. Res. 27
Norm. En. per Res. -3.7048
Hub Node A(2)
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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 -32.0726 28.9859 368.325 365.2383 198 26 15 16459 1 30 25
A-P -15.0831 -17.5809 -67.3654 -100.0293 27 3 1 2162 1 4 3
B-P 0.0 0.0 -77.2376 -77.2376 32 7 0 2564 0 3 0