6AT1
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 4
Strongest Interaction Chains B-D
Int. Res. 75
Norm. En. per Res. -4.8226
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 -40.2084 3.6616 -195.513 -232.0598 64 8 5 7082 3 31 26
A-D 0.0 0.0 -0.0027 -0.0027 2 0 0 4 0 0 0
B-D -80.0011 -44.5296 -237.166 -361.6968 75 15 5 8596 3 16 14
C-D -63.3585 -26.2555 -200.099 -289.7131 67 9 4 7237 4 30 25