1MCQ
principles and pitfalls in designing site directed peptide ligands
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains B-P
Int. Res. 17
Norm. En. per Res. -2.7576
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 -23.9897 25.4329 -381.261 -379.8178 195 37 17 16554 0 34 22
A-P 0.0 -10.0994 -9.7371 -19.8365 8 3 0 320 1 3 0
B-P 0.0 -15.2168 -31.6621 -46.8789 17 1 0 968 2 4 4