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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. -4.7864
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 -30.9287 2.8058 -190.121 -218.2439 68 5 5 7025 2 28 24
B-D -99.4782 -52.2022 -326.959 -478.6394 100 20 6 12067 4 26 25
C-D -65.0541 -13.7508 -194.444 -273.2489 64 6 5 7148 3 29 24