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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:

23卷

期数:

2017年05期

页码:

389-393

栏目:

基础医学

出版日期:

2017-09-20

文章信息/Info

Title:

Structural and Functional prediction of SRGAP1 in human

文章编号:

1006-8147(2017)05-0389-05

作者:

高红叶; 褚新雷; 李艳霞; 郑 红

(天津医科大学肿瘤医院肿瘤流行病与生物统计研究室,国家肿瘤临床医学研究中心,天津市“肿瘤防治”重点实验室,天津市恶性肿瘤临床医学研究中心,天津 300060)

Author(s):

GAO Hong-ye;  CHU Xin-lei;  LI Yan-xia;  ZHENG Hong

( Department of Cancer Epidemiology and Biostatistics, Cancer Institute and Hospital,Tianjin Medical University ,National Clinical Research Center for Cancer, Tianjin? Key Laboratory of Cancer Prevention and Therapy, Tianjins Clinical Research Center for Cancer, Tianjin 300060,China)

关键词:

Slit-Robo GTP 酶激活蛋白1; 生物信息学;  结构; 功能

Keywords:

Slit-Robo GTPase activator protein 1;  bioinformatics;  structure;  function

分类号:

Q811.4

DOI:

-

文献标志码:

A

摘要:

目的: 利用生物信息学对人Slit-Robo GTP 酶激活蛋白1（SRGAP1） 蛋白质的理化性质，信号肽，亲水性/疏水性，跨膜区域，蛋白质二级结构、三级结构，蛋白质间的相互作用及GO注释进行预测分析。方法：使用多种分析软件对SRGAP1蛋白进行在线预测分析。结果：SRGAP1理化性质分析结果显示，人SRGAP1 蛋白有1 085个氨基酸，等电点为6.36；生物信息学预测分析结果显示，SRGAP1无信号肽,无跨膜结构的亲水不稳定蛋白质。二级结构存在19个α螺旋和11个β折叠，预测到10个与SRGAP1存在相互作用的蛋白。SRGAP1蛋白在调控GTP酶活性，细胞迁移，信号通路中有重要的作用。结论：系统预测分析了等电点为6.36的人SRGAP1蛋白理化性质、结构和功能，为将来探索SRGAP1具体功能和分子机制提供了一定的思路和理论基础。

?

Abstract:

Objective: To analyze the physical and chemical properties and structural functions of human Slit-Robo GTPase activator protein 1 (SRGAP1) by bioinformatics. Methods: SRGAP1 was predicted and analyzed by multiple analysis software online. Results: SRGAP1 protein was composed of 1 085 amino acids, with isoelectric point of 6.36. Predictive results suggested that it was a hydrophilic and unstable protein without signal peptide and transmembrane domain. The secondary structure predictive analysis showed that it contained 19 α-helices and 11 β-sheets. Ten proteins interacted with SRGAP1 were predicted. SRGAP1 played an important role in the regulation of small GTPase activity, cell migration and signal transduction. Conclusion:These results may provide some ideas and theoretical basis for further exploration of SRGAP1 functional studies and molecular mechanisms.

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备注/Memo

备注/Memo:

基金项目 国家自然科学基金资助项目(81470153)
作者简介 高红叶(1989-)，女，硕士在读，研究方向：生物化学与分子生物学；

- 通信作者：郑红，E-mail:zhengh1964@163.com。

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更新日期/Last Update: 2017-09-20