2BJ0
crystal structure of achbp from bulinus truncatus revals the conserved structural scaffold and sites of variation in nicotinic acetylcholine receptors
Total interactions analyzed 10
Total true interactions 5
Strongest Interaction Chains A-E
Int. Res. 135
Norm. En. per Res. -3.019
Hub Node A(2)
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 -42.8423 -16.5077 -300.561 -359.911 131 10 7 12880 2 39 39
A-E -63.0543 -10.1301 -334.383 -407.5674 135 12 7 13982 1 41 40
B-C -34.6075 -5.5951 -293.873 -334.0756 134 11 7 12976 2 40 36
C-D -29.7456 -15.2683 -294.969 -339.9829 132 11 8 12671 4 39 39
D-E -30.0742 -1.5314 -283.061 -314.6666 131 14 7 12732 2 38 35