1PN3
crystal structure of tdp-epi-vancosaminyltransferase gtfa in complexes with tdp and the acceptor substrate dvv.
Total interactions analyzed 6
Total true interactions 3
Strongest Interaction Chains B-D
Int. Res. 25
Norm. En. per Res. -2.1098
Hub Node A(2)
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 -10.805 4.7628 -177.501 -183.5432 92 13 3 7225 1 34 40
A-C -12.2778 0.0 -34.2241 -46.5019 24 1 0 1121 0 0 0
B-D -18.0866 0.0 -34.6577 -52.7443 25 2 0 1214 0 0 0