1VMK
crystal structure of purine nucleoside phosphorylase (tm1596) from thermotoga maritima at 2.01 a resolution
Total interactions analyzed 3
Total true interactions 3
Strongest Interaction Chains A-C
Int. Res. 84
Norm. En. per Res. -4.2538
Hub Node A(2)
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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 -64.1742 -10.1167 -279.961 -354.2518 84 12 8 10741 0 15 18
A-C -58.0738 -8.9366 -290.311 -357.3214 84 11 9 10972 0 15 19
B-C -61.3885 -10.5909 -279.188 -351.1673 84 10 8 10846 0 15 18