1RAG
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. 100
Norm. En. per Res. -4.966
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 -29.8029 5.1806 -178.794 -203.4164 67 2 4 6863 2 28 23
B-D -94.8629 -61.6779 -340.058 -496.5989 100 26 6 12534 7 27 26
C-D -41.0706 -11.357 -194.093 -246.5207 63 7 5 7162 2 28 24