Galperin Michael Y, Moroz Olga V, Wilson Keith S, Murzin Alexey G
National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.
Mol Microbiol. 2006 Jan;59(1):5-19. doi: 10.1111/j.1365-2958.2005.04950.x.
Cellular metabolism constantly generates by-products that are wasteful or even harmful. Such compounds are excreted from the cell or are removed through hydrolysis to normal cellular metabolites by various 'house-cleaning' enzymes. Some of the most important contaminants are non-canonical nucleoside triphosphates (NTPs) whose incorporation into the nascent DNA leads to increased mutagenesis and DNA damage. Enzymes intercepting abnormal NTPs from incorporation by DNA polymerases work in parallel with DNA repair enzymes that remove lesions produced by modified nucleotides. House-cleaning NTP pyrophosphatases targeting non-canonical NTPs belong to at least four structural superfamilies: MutT-related (Nudix) hydrolases, dUTPase, ITPase (Maf/HAM1) and all-alpha NTP pyrophosphatases (MazG). These enzymes have high affinity (Km's in the micromolar range) for their natural substrates (8-oxo-dGTP, dUTP, dITP, 2-oxo-dATP), which allows them to select these substrates from a mixture containing a approximately 1000-fold excess of canonical NTPs. To date, many house-cleaning NTPases have been identified only on the basis of their side activity towards canonical NTPs and NDP derivatives. Integration of growing structural and biochemical data on these superfamilies suggests that their new family members cleanse the nucleotide pool of the products of oxidative damage and inappropriate methylation. House-cleaning enzymes, such as 6-phosphogluconolactonase, are also part of normal intermediary metabolism. Genomic data suggest that house-cleaning systems are more abundant than previously thought and include numerous analogous enzymes with overlapping functions. We discuss the structural diversity of these enzymes, their phylogenetic distribution, substrate specificity and the problem of identifying their true substrates.
细胞代谢不断产生一些无用甚至有害的副产物。这些化合物会从细胞中排出,或者通过各种“清理”酶水解为正常的细胞代谢物而被清除。一些最重要的污染物是非经典核苷三磷酸(NTP),其掺入新生DNA会导致诱变增加和DNA损伤。拦截DNA聚合酶掺入异常NTP的酶与去除修饰核苷酸产生的损伤的DNA修复酶协同工作。靶向非经典NTP的清理NTP焦磷酸酶至少属于四个结构超家族:MutT相关(Nudix)水解酶、dUTPase、ITPase(Maf/HAM1)和全α NTP焦磷酸酶(MazG)。这些酶对其天然底物(8-氧代-dGTP、dUTP、dITP、2-氧代-dATP)具有高亲和力(Km值在微摩尔范围内),这使它们能够从含有大约1000倍过量经典NTP的混合物中选择这些底物。迄今为止,许多清理NTP酶仅根据它们对经典NTP和NDP衍生物的副活性来鉴定。关于这些超家族不断增长的结构和生化数据的整合表明,它们的新家族成员清理了氧化损伤和不适当甲基化产物的核苷酸池。清理酶,如6-磷酸葡萄糖酸内酯酶,也是正常中间代谢的一部分。基因组数据表明,清理系统比以前认为的更为丰富,包括许多功能重叠的类似酶。我们讨论了这些酶的结构多样性、它们的系统发育分布、底物特异性以及鉴定其真正底物的问题。