1QSH
magnesium(ii)-and zinc(ii)-protoporphyrin ix's stabilize the lowest oxygen affinity state of human hemoglobin even more strongly than deoxyheme
Total interactions analyzed 6
Total true interactions 6
Strongest Interaction Chains A-C
Int. Res. 46
Norm. En. per Res. -3.3421
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 -17.5373 13.2593 -247.853 -252.131 90 5 8 9442 0 17 19
A-C -27.0851 -70.792 -55.8611 -153.7382 46 2 0 2127 4 8 11
A-D -28.0752 36.5333 -182.982 -174.5239 59 4 0 6605 2 20 19
B-C -27.0693 34.0266 -184.365 -177.4076 60 9 0 6858 0 20 19
B-D 0.0 0.0 -0.001 -0.001 6 0 0 3 0 2 12
C-D -25.4766 11.4294 -253.03 -267.0772 90 8 8 9744 0 18 19