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人FoxO3蛋白的生物信息学分析

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本文利用生物信息学技术预测和分析人FoxO3蛋白的生物学特性,预测其二级、三级结构及相应特征表现,以期为与人FoxO3蛋白相关的疾病提供有效机制以及可能的干预靶点作为参考。本文主要从NCBI中获取人FoxO3蛋白序列,并利用ProtParam、SignalP等分析工具对其理化性质、磷酸化位点、二级/三级结构以及上下游相关关联蛋白作用等方面进行分析和预测。结果表明,人FoxO3蛋白由673个氨基酸残基组成,等电点为4。98,是不稳定的亲水蛋白质,其相对分子质量为71。3 kD,具有114个磷酸化位点。其主要二级结构是α—螺旋,不含信号肽和跨膜区,结构上含一个FORK_HEAD结构域。FoxO3能与多种SIRT1、AKT1等蛋白发生相互作用。人FoxO3蛋白作为一种具有114个磷酸化位点的不稳定的亲水蛋白,在乙酰化、磷酸化、Wnt通路等方面具有重要作用。
Bioinformatic Analysis of Human FoxO3 Protein
To predict the structure and function of human FoxO3 protein with bioinformatics.Bioinformatic tools were used to predict physical and chemical properties.Human FoxO3 contained 673 amino acid residues.The theoretical isoelectric point was 4.98,the calculated molecular mass was 71.3kD,and it was highly conservative in mammal.The signal peptide and transmembrane regions were not found in human FoxO3.The main compositions of protein secondary structure were alpha.helix.beta.extended strand and random coil.which contained one FORK_HEAD domain.The proteins interaction with human FoxO3 were SIRT1、AKT1.Conclusion:Human FoxO3 protein is a hydrophile protein without signal peptide and transmembrane regions and involves in the activation of FoxO signal pathway may play an important role in oxidative stress and tumor progress.Our research can provide useful information for the further study of human FoxO3.

FoxO3sequence analysisbioinformatic analysisoxidative stress

谌业帅、孟利、朱梁

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徐州医科大学附属医院,江苏 徐州 221000

徐州医科大学,江苏省脑病生物信息重点实验室,江苏 徐州 221004

FoxO3 序列分析 生物信息学分析 氧化应激

2024

中国科技纵横
中国民营科技促进会

中国科技纵横

影响因子:0.102
ISSN:1671-2064
年,卷(期):2024.(22)