1RAI
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. 89
Norm. En. per Res. -5.1237
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 -39.1417 6.2466 -187.092 -219.9871 66 5 5 7053 2 28 25
B-D -93.1999 -48.4715 -314.336 -456.0074 89 23 6 11744 4 23 19
C-D -60.0906 -1.9957 -188.934 -251.0203 64 6 4 7103 4 28 24