Part 5: Algorithm to computationally estimate the effect of Pi for 4 LDH enzymes
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In order to estimate whether Pi has an activatory or an inhibitory effect on the enzymes, the computed probe binding energies (from GRID results, Part 4) were compared with those for the LDH from L. plantarum whose activity is known to be unaffected by Pi.

The binding energies of the Pi probe in the allosteric binding site (AS) and the COO probe in the catalytic binding site (CS) of LDH from L. plantarum were defined as E¬AS,threshold and ECS,threshold, respectively. For the other LDH enzymes, the activity was considered to be enhanced by Pi, if the binding energy of the Pi probe in the allosteric binding site, EPi ≤ E-AS,threshold. When the binding energy of Pi in the catalytic site EPi ≥ ECS,threshold, no inhibition by Pi was anticipated. The magnitude of activation and inhibition by Pi was assessed by computing and analyzing the following energy differences: ΔEAS = EPi - EAS,threshold; ΔECS = EPi - ECS,threshold; = EPi - ECOO¬. A strong enhancement of enzyme activity (designated by letter A) was assigned, if ΔEAS ≤ -2 kcal/mol. The letter a designates weak activation, when -2 ≤ ΔEAS ≤ 0 kcal/mol. Strong inhibition (I) was assigned when both ΔECS < 0 and ≤ -2 kcal/mol. Weak inhibition (i) was assumed when both ΔECS < 0 and -2 ≤ ≤ 0 kcal/mol. For ΔECS ≥ 0, no competition between Pi and COO in the catalytic site, and thus no inhibition, was expected (¬I). The following relations were used to deduce the overall effect of the presence of Pi considering the possibility of Pi binding at the allosteric site and the catalytic site: A∧¬I A; a∧¬I a; ☐∧¬I ¬E (no effect); A∧i a∨¬E; ☐∧i i; A∧I ¬E∨i; ☐∧I I. Here, we use the common logical connectives (30) ∧ for “AND”, ∨ for “OR”, ¬ for negation “NOT” and ☐ for the cases when the allosteric binding site is occupied by FBP and thus not accessible for Pi.


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Organism: Lactic acid bacteria

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Views: 4330   Downloads: 153

Created: 10th Jun 2014 at 14:19

Last updated: 10th Jun 2014 at 14:49

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Version 1 Created 10th Jun 2014 at 14:19 by Anna Feldman-Salit

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