2DVA
crystal structure of peanut lectin gal-beta-1,3-galnac- alpha-o-me (methyl-t-antigen) complex
Total interactions analyzed 6
Total true interactions 6
Strongest Interaction Chains C-D
Int. Res. 76
Norm. En. per Res. -2.9426
Hub Node A(3)
Click on the Nodes or Edges in the network to see the details
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 0.0 0.0 -131.652 -131.652 74 6 2 6161 0 4 4
A-C -7.9626 0.0 -10.2538 -18.2164 10 1 0 356 0 0 0
A-D -12.3218 0.0 -259.146 -271.4678 103 19 8 11283 0 7 7
B-C -10.1937 0.0 -260.277 -270.4707 103 16 9 11295 0 6 7
B-D -4.3536 0.0 -9.7327 -14.0863 9 1 0 340 0 0 0
C-D -39.8753 -63.9139 -119.845 -223.6342 76 18 2 6136 6 12 4