1MT7
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. 117
Norm. En. per Res. -6.3467
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 -166.8739 -7.0365 -568.648 -742.5584 117 39 15 20684 1 8 4
A-P -73.428 0.0 -125.4 -198.828 40 14 4 4759 0 0 0
B-P -24.0878 0.0 -95.7772 -119.865 41 6 5 4017 0 0 0