2FZK
the structure of wild-type e. coli aspartate transcarbamoylase in complex with novel t state inhibitors at 2.50 resolution
Total interactions analyzed 6
Total true interactions 3
Strongest Interaction Chains B-D
Int. Res. 87
Norm. En. per Res. -4.5187
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 -48.0723 -14.1311 -199.251 -261.4544 71 13 5 7434 2 28 25
B-D -101.2582 -37.5893 -254.282 -393.1295 87 25 7 11157 2 23 21
C-D -52.2518 1.4372 -197.757 -248.5716 69 11 5 7155 1 26 24