2V92
crystal structure of the regulatory fragment of mammalian ampk in complexes with atp-amp
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains A-B
Int. Res. 109
Norm. En. per Res. -6.3034
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 -140.6326 -24.0727 -522.365 -687.0703 109 17 17 18401 2 16 16
A-E -25.2807 13.9983 -177.35 -188.6324 75 12 4 6854 0 10 15
B-E -119.1571 -13.1393 -253.183 -385.4794 89 18 12 10586 0 20 19