Stein Matthias, Gabdoulline Razif R, Wade Rebecca C
Molecular and Cellular Modeling Group, EML Research gGmbH, Schloss-Wolfsbrunnenweg 33, 69118 Heidelberg, Germany.
Biochem Soc Trans. 2008 Feb;36(Pt 1):51-4. doi: 10.1042/BST0360051.
Enzyme kinetic parameters can differ between different species and isoenzymes for the same catalysed reaction. Computational approaches to calculate enzymatic kinetic parameters from the three-dimensional structures of proteins will be reviewed briefly here. Enzyme kinetic parameters may be derived by modelling and simulating the rate-determining process. An alternative, approximate, but more computationally efficient approach is the comparison of molecular interaction fields for experimentally characterized enzymes and those for which parameters should be determined. A correlation between differences in interaction fields and experimentally determined kinetic parameters can be used to determine parameters for orthologous enzymes from other species. The estimation of enzymatic kinetic parameters is an important step in setting up mathematical models of biochemical pathways in systems biology.
对于同一催化反应,不同物种和同工酶的酶动力学参数可能会有所不同。本文将简要综述从蛋白质三维结构计算酶动力学参数的计算方法。酶动力学参数可通过对速率决定过程进行建模和模拟得出。另一种替代方法虽然近似,但计算效率更高,即比较实验表征酶与待确定参数酶的分子相互作用场。相互作用场差异与实验测定的动力学参数之间的相关性可用于确定其他物种直系同源酶的参数。酶动力学参数的估计是建立系统生物学中生化途径数学模型的重要一步。