2DBU
crystal structure of gamma-glutamyltranspeptidase from escherichia coli
Total interactions analyzed 6
Total true interactions 6
Strongest Interaction Chains A-B
Int. Res. 446
Norm. En. per Res. -5.8893
Hub Node A(3)
Click on the Nodes or Edges in the network to see the details
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 -513.4609 -112.1799 -2001.0 -2626.6407 446 90 67 74610 9 98 93
A-C 0.0 -54.5702 -16.7517 -71.3219 35 3 0 1206 5 21 27
A-D -17.9032 23.1048 -101.28 -96.0784 54 3 1 4079 1 24 19
B-C -18.029 25.0396 -104.075 -97.0644 54 5 1 4258 1 24 20
B-D -21.4004 -25.4992 -40.8332 -87.7329 44 4 0 2139 4 11 10
C-D -494.6061 -87.0855 -1998.79 -2580.4816 449 88 66 74393 6 97 94