1RAC
crystal structure of ctp-ligated t state aspartate transcarbamoylase at 2.5 angstroms resolution: implications for atcase mutants and the mechanism of negative cooperativity
Total interactions analyzed 6
Total true interactions 3
Strongest Interaction Chains B-D
Int. Res. 97
Norm. En. per Res. -4.667
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 -37.5285 0.1503 -189.677 -227.0552 69 5 5 7067 2 27 24
B-D -92.1034 -54.3666 -306.233 -452.703 97 33 5 11831 6 26 26
C-D -50.2441 -13.3179 -191.396 -254.958 64 6 5 7079 2 28 24