2A0F
structure of d236a mutant e. coli aspartate transcarbamoylase in presence of phosphonoacetamide at 2.90 a resolution
Total interactions analyzed 6
Total true interactions 3
Strongest Interaction Chains B-D
Int. Res. 75
Norm. En. per Res. -4.5519
Hub Node A(1)
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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 -68.3453 16.6964 -190.525 -242.1739 83 35 3 8691 1 39 29
B-D -89.1482 -58.5569 -193.685 -341.3901 75 78 5 10443 6 17 15
C-D -13.9821 -19.5851 -113.469 -147.0363 73 24 3 7060 1 35 28