1LYA
crystal structures of native and inhibited forms of human cathepsin d: implications for lysosomal targeting and drug design
Total interactions analyzed 6
Total true interactions 4
Strongest Interaction Chains A-B
Int. Res. 207
Norm. En. per Res. -7.4875
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 -440.2786 -2.8378 -1106.79 -1549.9065 207 63 33 39441 1 29 31
A-D -6.1584 0.0 -11.32 -17.4784 18 2 0 642 0 2 4
B-D -5.8795 0.0 -21.5348 -27.4143 25 0 0 1015 0 3 4
C-D -457.5963 -8.7304 -1087.44 -1553.7667 209 59 31 39137 3 28 31