1RAE
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. 96
Norm. En. per Res. -5.1128
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 -32.9694 2.8909 -186.736 -216.8145 68 3 5 6986 2 28 24
B-D -109.4861 -51.7492 -329.597 -490.8323 96 27 5 12112 5 26 25
C-D -48.9929 -10.5333 -192.259 -251.7851 64 5 5 7090 2 29 24