Shen Pei, Zhang Hong, Su Zhaoliang, Wang Shengjun, Xu Huaxi
Department of Immunology, Institute of Laboratory Medicine, Jiangsu University, Zhenjiang, Jiangsu, People's Republic of China; Laboratory Medicine Center, Affiliated Hospital of Nantong University, Nantong, Jiangsu, People's Republic of China.
Department of Clinical Laboratory, Nantong Rich Hospital, The Fourth Clinical College of Yangzhou University, Nantong, Jiangsu, People's Republic of China.
PLoS One. 2015 Jul 24;10(7):e0134114. doi: 10.1371/journal.pone.0134114. eCollection 2015.
Tumor necrosis factor α-induced protein 8 (TNFAIP8)-like protein 1 (TIPE1) was a member of TNFAIP8 family. Previous studies have shown that TIPE1 could induce apoptosis in hepatocellular carcinoma. In this study, we attempted to predict its potential structure. Bioinformatic analysis of TIPE1 was performed to predict its potential structure using the bioinfomatic web services or softwares. The results showed that the amino acid sequences of TIPE1 were well conserved in mammals. No signal peptide and no transmembrane domain existed in human TIPE1. The aliphatic index of TIPE1 was 100.75 and the theoretical pI was 9.57. TIPE1 was a kind of stable protein and its grand average of hydropathicity was -0.108. Various post-translational modifications were also speculated to exist in TIPE1. In addition, the results of Swiss-Model Server and Swiss-Pdb Viewer program revealed that the predicted three-dimensional structure of TIPE1 protein was stable and it may accord with the rule of stereochemistry. TIPE1 was predicted to interact with FBXW5, caspase8 and so on. In conclusion, TIPE1 may be a stable protein with no signal peptide and no transmembrane domain. The bioinformatic analysis of TIPE1 will provide the basis for the further study on the function of TIPE1.
肿瘤坏死因子α诱导蛋白8(TNFAIP8)样蛋白1(TIPE1)是TNFAIP8家族的成员。先前的研究表明,TIPE1可诱导肝癌细胞凋亡。在本研究中,我们试图预测其潜在结构。利用生物信息学网络服务或软件对TIPE1进行生物信息学分析,以预测其潜在结构。结果表明,TIPE1的氨基酸序列在哺乳动物中高度保守。人TIPE1不存在信号肽和跨膜结构域。TIPE1的脂肪族指数为100.75,理论pI为9.57。TIPE1是一种稳定的蛋白质,其亲水性总平均值为-0.108。还推测TIPE1存在多种翻译后修饰。此外,Swiss-Model Server和Swiss-Pdb Viewer程序的结果显示,TIPE1蛋白的预测三维结构是稳定的,可能符合立体化学规则。预测TIPE1与FBXW5、半胱天冬酶8等相互作用。总之,TIPE1可能是一种无信号肽和跨膜结构域的稳定蛋白质。对TIPE1的生物信息学分析将为进一步研究TIPE1的功能提供依据。