Lepesheva Galina I, Waterman Michael R
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, USA.
Biochim Biophys Acta. 2011 Jan;1814(1):88-93. doi: 10.1016/j.bbapap.2010.06.006. Epub 2010 Jun 11.
Sterol 14α-demethylases (14DM) comprise the CYP51 cytochrome P450 genome family. The 14DM reaction is essential for the biosynthesis of sterols which are necessary for production of cellular membranes. This is the most widely distributed P450, being present in all biological kingdoms. From one kingdom to another the primary amino acid sequence identity usually ranges between 30 and 20%. In this minireview we describe the conservation of specific amino acids and the various CYP51 orthologs and indicate the roles that they may play in the structure/function of this monooxygenase. The prediction of the roles of different amino acids in 14DM is based on high resolution tertiary structures of these enzymes which set the stage for detailed understanding of the 14α-demethylase reaction and its selective, phyla-specific inhibition which is crucial for the design of potent inhibitors for treatment of infection by pathogenic microbes.
甾醇14α-脱甲基酶(14DM)属于CYP51细胞色素P450基因组家族。14DM反应对于甾醇的生物合成至关重要,而甾醇是细胞膜生成所必需的。这是分布最为广泛的P450,存在于所有生物界。在不同生物界之间,其一级氨基酸序列同一性通常在30%至20%之间。在这篇小型综述中,我们描述了特定氨基酸的保守性以及各种CYP51直系同源物,并指出它们在这种单加氧酶的结构/功能中可能发挥的作用。对14DM中不同氨基酸作用的预测基于这些酶的高分辨率三级结构,这为详细理解14α-脱甲基酶反应及其选择性、门特异性抑制奠定了基础,而这种抑制对于设计用于治疗病原微生物感染的有效抑制剂至关重要。