1XG3
crystal structure of the c123s 2-methylisocitrate lyase mutant from escherichia coli in complex with the reaction product, mg(ii)-pyruvate and succinate
Total interactions analyzed 6
Total true interactions 6
Strongest Interaction Chains A-B
Int. Res. 286
Norm. En. per Res. -5.2755
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 -159.3757 -180.7842 -1168.62 -1508.7799 286 30 47 44589 31 82 84
A-C -3.4367 49.7629 -115.588 -69.2618 74 8 4 5200 6 15 6
A-D -46.7351 -45.9281 -140.289 -232.9522 99 7 3 5968 2 26 38
B-C -49.2429 -46.4719 -156.499 -252.2138 101 6 3 6367 2 27 39
B-D -6.8041 44.3661 -122.175 -84.613 72 8 4 5438 6 13 6
C-D -129.426 -130.582 -1116.51 -1376.5179 276 35 45 42760 22 76 78