5AT1
structural consequences of effector binding to the t state of aspartate carbamoyltransferase. crystal structures of the unligated and atp-, and ctp-complexed enzymes at 2.6-angstroms resolution
Total interactions analyzed 6
Total true interactions 3
Strongest Interaction Chains B-D
Int. Res. 80
Norm. En. per Res. -4.4177
Hub Node A(1)
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 -31.647 -10.7665 -194.673 -237.0865 63 8 5 7180 5 27 27
B-D -85.1991 -20.425 -247.79 -353.4141 80 18 6 9547 2 18 14
C-D -48.9754 -39.9191 -199.027 -287.9216 67 10 5 7270 3 34 26