Domitrovic Tatiana, Raymundo Diana P, da Silva Tiago Fernandes, Palhano Fernando L
Departamento de Virologia, Instituto de Microbiologia Paulo de Goes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Programa de Biologia Estrutural, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
PLoS One. 2015 Sep 1;10(9):e0136761. doi: 10.1371/journal.pone.0136761. eCollection 2015.
Pyridoxinamine 5'-phosphate oxidases (P(N/M)P oxidases) that bind flavin mononucleotide (FMN) and oxidize pyridoxine 5'-phosphate or pyridoxamine 5'-phosphate to form pyridoxal 5'-phosphate (PLP) are an important class of enzymes that play a central role in cell metabolism. Failure to generate an adequate supply of PLP is very detrimental to most organisms and is often clinically manifested as a neurological disorder in mammals. In this study, we analyzed the function of YLR456W and YPR172W, two homologous genes of unknown function from S. cerevisiae that have been annotated as putative P(N/M)P oxidases based on sequence homology. Different experimental approaches indicated that neither protein catalyzes PLP formation nor binds FMN. On the other hand, our analysis confirmed the enzymatic activity of Pdx3, the S. cerevisiae protein previously implicated in PLP biosynthesis by genetic and structural characterization. After a careful sequence analysis comparing the putative and confirmed P(N/M)P oxidases, we found that the protein domain (PF01243) that led to the YLR456W and YPR172W annotation is a poor indicator of P(N/M)P oxidase activity. We suggest that a combination of two Pfam domains (PF01243 and PF10590) present in Pdx3 and other confirmed P(N/M)P oxidases would be a stronger predictor of this molecular function. This work exemplifies the importance of experimental validation to rectify genome annotation and proposes a revision in the annotation of at least 400 sequences from a wide variety of fungal species that are homologous to YLR456W and are currently misrepresented as putative P(N/M)P oxidases.
结合黄素单核苷酸(FMN)并将5'-磷酸吡哆醇或5'-磷酸吡哆胺氧化形成5'-磷酸吡哆醛(PLP)的5'-磷酸吡哆胺氧化酶(P(N/M)P氧化酶)是一类重要的酶,在细胞代谢中起核心作用。无法产生足够的PLP对大多数生物体非常有害,在哺乳动物中通常临床表现为神经紊乱。在本研究中,我们分析了酿酒酵母中两个功能未知的同源基因YLR456W和YPR172W的功能,基于序列同源性,它们已被注释为假定的P(N/M)P氧化酶。不同的实验方法表明,这两种蛋白质都不催化PLP的形成,也不结合FMN。另一方面,我们的分析证实了Pdx3的酶活性,Pdx3是酿酒酵母中的一种蛋白质,先前已通过遗传和结构表征参与PLP生物合成。在仔细比较假定的和已证实的P(N/M)P氧化酶的序列后,我们发现导致YLR456W和YPR172W注释的蛋白质结构域(PF01243)并不能很好地指示P(N/M)P氧化酶活性。我们认为,Pdx3和其他已证实的P(N/M)P氧化酶中存在的两个Pfam结构域(PF01243和PF10590)的组合将是这种分子功能更强的预测指标。这项工作例证了实验验证对纠正基因组注释的重要性,并建议对来自多种真菌物种的至少400个与YLR456W同源且目前被错误表征为假定的P(N/M)P氧化酶的序列的注释进行修订。