Binding Sites of Bicarbonate in Phosphoenolpyruvate Carboxylase

被引:1
|
作者
Cheron, Nicolas [1 ]
机构
[1] Sorbonne Univ, PSL Univ, Dept Chim, PASTEUR,Ecole Normale Super,CNRS, F-75005 Paris, France
关键词
FREE-ENERGY CALCULATIONS; DIRECTED MUTAGENESIS; 3-DIMENSIONAL STRUCTURE; FLAVERIA-TRINERVIA; MAIZE; SEDOHEPTULOSE-1,7-BISPHOSPHATASE; INHIBITORS; MECHANISM; FRONTIERS; RESIDUE;
D O I
10.1021/acs.jcim.3c01830
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Phosphoenolpyruvate carboxylase (PEPC) is used in plant metabolism for fruit maturation or seed development as well as in the C4 and crassulacean acid metabolism (CAM) mechanisms in photosynthesis, where it is used for the capture of hydrated CO2 (bicarbonate). To find the yet unknown binding site of bicarbonate in this enzyme, we have first identified putative binding sites with nonequilibrium molecular dynamics simulations and then ranked these sites with alchemical free energy calculations with corrections of computational artifacts. Fourteen pockets where bicarbonate could bind were identified, with three having realistic binding free energies with differences with the experimental value below 1 kcal/mol. One of these pockets is found far from the active site at 14 angstrom and predicted to be an allosteric binding site. In the two other binding sites, bicarbonate is in direct interaction with the magnesium ion; neither sequence alignment nor the study of mutant K606N allowed to discriminate between these two pockets, and both are good candidates as the binding site of bicarbonate in phosphoenolpyruvate carboxylase.
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页码:3375 / 3385
页数:11
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