4AT1
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. 76
Norm. En. per Res. -4.4628
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 -56.1521 -2.6042 -192.193 -250.9493 65 5 5 6997 3 30 26
B-D -92.2221 -15.3723 -231.581 -339.1755 76 22 4 8992 0 15 13
C-D -40.1854 1.576 -186.025 -224.6344 66 4 5 6996 3 33 26