2C3D
2.15 angstrom crystal structure of 2-ketopropyl coenzyme m oxidoreductase carboxylase with a coenzyme m disulfide bound at the active site
Total interactions analyzed 1
Total true interactions 1
Strongest Interaction Chains A-B
Int. Res. 402
Norm. En. per Res. -3.8344
Hub Node A(1)
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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 -99.8516 -122.2311 -1319.35 -1541.4327 402 52 35 52822 14 102 90