1RAB
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. -4.7449
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 -31.438 -13.0521 -189.229 -233.7191 71 3 5 7034 3 28 24
B-D -96.3134 -57.1323 -321.047 -474.4927 100 30 5 12033 6 26 27
C-D -51.1173 -1.3021 -196.173 -248.5924 64 6 5 7137 3 28 24