Department of Biochemistry, University of Cambridge , Cambridge , UK.
Front Immunol. 2013 Oct 7;4:317. doi: 10.3389/fimmu.2013.00317. eCollection 2013.
Amino acids with functional or key structural roles display higher degrees of conservation through evolution. The comparative analysis of protein sequences from multiple species and/or between homologous proteins can be highly informative in the identification of key structural and functional residues. Residues which in turn provide insight into the molecular mechanisms of protein function. We have explored the genomic and amino acid conservation of the prototypic innate immune genes NOD1 and NOD2. NOD1 orthologs were found in all vertebrate species analyzed, whilst NOD2 was absent from the genomes of avian, reptilian and amphibian species. Evolutionary trace analysis was used to identify highly conserved regions of NOD1 and NOD2 across multiple species. Consistent with the known functions of NOD1 and NOD2 highly conserved patches were identified that matched the Walker A and B motifs and provided interaction surfaces for the adaptor protein RIP2. Other patches of high conservation reflect key structural functions as predicted by homology models. In addition, the pattern of residue conservation within the leucine-rich repeat (LRR) region of NOD1 and NOD2 is indicative of a conserved mechanism of ligand recognition involving the concave surface of the LRRs.
具有功能或关键结构作用的氨基酸在进化过程中表现出更高程度的保守性。对来自多个物种的蛋白质序列或同源蛋白质之间的比较分析,可以在识别关键结构和功能残基方面提供非常有价值的信息。这些残基反过来又为蛋白质功能的分子机制提供了深入的了解。我们已经探索了典型先天免疫基因 NOD1 和 NOD2 的基因组和氨基酸保守性。在分析的所有脊椎动物物种中都发现了 NOD1 的同源物,而 NOD2 则不存在于鸟类、爬行动物和两栖动物的基因组中。进化轨迹分析用于识别 NOD1 和 NOD2 在多个物种中的高度保守区域。与 NOD1 和 NOD2 的已知功能一致,鉴定出了高度保守的斑块,这些斑块与 Walker A 和 B 基序匹配,并为衔接蛋白 RIP2 提供了相互作用表面。其他高度保守的斑块反映了同源建模预测的关键结构功能。此外,NOD1 和 NOD2 的富含亮氨酸重复(LRR)区域内残基的保守模式表明涉及 LRRs 凹面的配体识别存在保守机制。