Laughton C A, Zvelebil M J, Neidle S
CRC Biomolecular Structure Unit, Institute of Cancer Research, Sutton, Surrey, England.
J Steroid Biochem Mol Biol. 1993 Mar;44(4-6):399-407. doi: 10.1016/0960-0760(93)90243-p.
Using a variety of techniques, including sequence alignment, secondary structure prediction, molecular mechanics and molecular dynamics, we have constructed a model for the three-dimensional structure of P-450arom (human aromatase) based on that of P-450cam, the only cytochrome P-450 enzyme for which the crystal structure is known. The predicted structure is found to be in good agreement with current experimental data; both direct, from site-directed mutagenesis studies, and indirect, from the consideration of the structures and activities of known substrates and inhibitors.
我们运用了多种技术,包括序列比对、二级结构预测、分子力学和分子动力学,基于已知晶体结构的唯一细胞色素P-450酶P-450cam,构建了P-450arom(人芳香化酶)的三维结构模型。预测的结构与当前的实验数据高度吻合;这些数据既有来自定点诱变研究的直接数据,也有来自对已知底物和抑制剂的结构与活性的考量的间接数据。