1RAD
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. 98
Norm. En. per Res. -5.034
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 -35.8229 -13.9925 -189.128 -238.9435 69 7 5 6996 2 28 24
B-D -107.1852 -45.6315 -340.513 -493.3296 98 31 5 12432 4 27 26
C-D -47.3541 -15.2331 -188.622 -251.2092 65 4 4 6959 3 28 24