3PI8
site-specific glycosylation of hemoglobin utilizing oxime ligation chemistry as a viable alternative to pegylation
Total interactions analyzed 6
Total true interactions 6
Strongest Interaction Chains A-B
Int. Res. 92
Norm. En. per Res. -3.1792
Hub Node A(3)
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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 -26.7403 10.0911 -275.841 -292.4902 92 7 12 10533 0 16 17
A-C -9.8604 -0.0018 -93.2315 -103.0937 55 5 6 3982 0 8 14
A-D -7.01 11.2183 -113.51 -109.3017 59 2 0 4581 0 15 11
B-C -5.3651 1.3921 -114.805 -118.778 57 2 0 4551 0 15 11
B-D 0.0 25.6893 -36.5143 -10.825 29 0 0 1149 0 10 21
C-D -23.2142 16.5674 -263.835 -270.4818 91 9 12 10450 0 16 18