1MT9
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. 115
Norm. En. per Res. -6.8826
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 -182.1464 -43.3522 -565.995 -791.4936 115 28 14 20485 4 8 4
A-P -43.0499 0.0 -92.4903 -135.5402 39 7 5 3934 0 2 5
B-P -61.2212 -34.4056 -154.343 -249.9698 49 21 6 6170 1 3 6