1MT8
viability of a drug-resistant hiv-1 protease mutant: structural insights for better antiviral therapy
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains A-B
Int. Res. 110
Norm. En. per Res. -6.8782
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 -174.8254 -44.4062 -537.371 -756.6025 110 38 14 19532 4 8 4
A-P -46.304 -9.5603 -86.8153 -142.6797 37 8 11 4034 0 4 3
B-P -59.7847 51.4376 -114.287 -122.6341 42 7 8 4608 0 5 5