• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人PRMT5使OCTR-1和人α-2A肾上腺素能受体在第三个细胞内环内发生甲基化。

The OCTR-1 and Human Alpha-2A Adrenergic Receptors are Methylated within the Third Intracellular Loop by Human PRMT5 .

作者信息

Bowitch Alexander, Chinsky Tyler M, Yu Michael C, Ferkey Denise M

机构信息

Department of Biological Sciences, University at Buffalo, The State University of New York, Buffalo, NY 14260 USA.

出版信息

MicroPubl Biol. 2022 Mar 23;2022. doi: 10.17912/micropub.biology.000546. eCollection 2022.

DOI:10.17912/micropub.biology.000546
PMID:35622502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9007614/
Abstract

Arginines within the third intracellular loop of the OCTR-1 and human ADRA2A receptors are methylated by the human protein arginine methyltransferase PRMT5 . Methylation of these residues could serve to modulate receptor signaling .

摘要

人OCTR-1和人ADRA2A受体第三个细胞内环中的精氨酸被人蛋白质精氨酸甲基转移酶PRMT5甲基化。这些残基的甲基化可能有助于调节受体信号传导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc5d/9007614/985f65968472/25789430-2022-micropub.biology.000546.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc5d/9007614/985f65968472/25789430-2022-micropub.biology.000546.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc5d/9007614/985f65968472/25789430-2022-micropub.biology.000546.jpg

相似文献

1
The OCTR-1 and Human Alpha-2A Adrenergic Receptors are Methylated within the Third Intracellular Loop by Human PRMT5 .人PRMT5使OCTR-1和人α-2A肾上腺素能受体在第三个细胞内环内发生甲基化。
MicroPubl Biol. 2022 Mar 23;2022. doi: 10.17912/micropub.biology.000546. eCollection 2022.
2
alpha 2A/alpha 2C-adrenergic receptor third loop chimera show that agonist interaction with receptor subtype backbone establishes G protein-coupled receptor kinase phosphorylation.α2A/α2C肾上腺素能受体第三环嵌合体表明,激动剂与受体亚型主干的相互作用可建立G蛋白偶联受体激酶磷酸化。
J Biol Chem. 2000 Sep 15;275(37):28989-93. doi: 10.1074/jbc.M005381200.
3
Four consecutive serines in the third intracellular loop are the sites for beta-adrenergic receptor kinase-mediated phosphorylation and desensitization of the alpha 2A-adrenergic receptor.第三个细胞内环中的四个连续丝氨酸是β-肾上腺素能受体激酶介导的α2A-肾上腺素能受体磷酸化和脱敏的位点。
J Biol Chem. 1995 Mar 3;270(9):4681-8. doi: 10.1074/jbc.270.9.4681.
4
Immunohistochemical localization of alpha 2A-adrenergic receptors in catecholaminergic and other brainstem neurons in the rat.
Neuroscience. 1993 Sep;56(1):139-55. doi: 10.1016/0306-4522(93)90569-2.
5
The third intracellular loop of alpha 2-adrenergic receptors determines subtype specificity of arrestin interaction.α2-肾上腺素能受体的第三个细胞内环决定了抑制蛋白相互作用的亚型特异性。
J Biol Chem. 2002 Nov 8;277(45):43247-52. doi: 10.1074/jbc.M207495200. Epub 2002 Aug 29.
6
Neuronal GPCR OCTR-1 regulates innate immunity by controlling protein synthesis in Caenorhabditis elegans.神经元 GPCR OCTR-1 通过控制秀丽隐杆线虫中的蛋白质合成来调节先天免疫。
Sci Rep. 2016 Nov 11;6:36832. doi: 10.1038/srep36832.
7
Regulated interactions of the alpha 2A adrenergic receptor with spinophilin, 14-3-3zeta, and arrestin 3.α2A肾上腺素能受体与亲嗜素、14-3-3ζ和抑制蛋白3的调控相互作用。
J Biol Chem. 2002 Dec 27;277(52):50589-96. doi: 10.1074/jbc.M208503200. Epub 2002 Oct 9.
8
An asn to lys polymorphism in the third intracellular loop of the human alpha 2A-adrenergic receptor imparts enhanced agonist-promoted Gi coupling.
J Biol Chem. 2000 Dec 8;275(49):38518-23. doi: 10.1074/jbc.M004550200.
9
Two peptides from the alpha 2A-adrenergic receptor alter receptor G protein coupling by distinct mechanisms.来自α2A-肾上腺素能受体的两种肽通过不同机制改变受体与G蛋白的偶联。
J Biol Chem. 1991 Jun 15;266(17):11025-9.
10
Sites in the third intracellular loop of the alpha 2A-adrenergic receptor confer short term agonist-promoted desensitization. Evidence for a receptor kinase-mediated mechanism.
J Biol Chem. 1992 Mar 5;267(7):4740-6.

本文引用的文献

1
Methylation of the D2 dopamine receptor affects binding with the human regulatory proteins Par-4 and Calmodulin.D2多巴胺受体的甲基化会影响其与人类调节蛋白Par-4和钙调蛋白的结合。
MicroPubl Biol. 2021 Feb 9;2021. doi: 10.17912/micropub.biology.000366.
2
The Protein Arginine Methyltransferase PRMT-5 Regulates SER-2 Tyramine Receptor-Mediated Behaviors in .蛋白质精氨酸甲基转移酶PRMT-5调节秀丽隐杆线虫中SER-2酪胺受体介导的行为 。 (注:原文中“. ”处似乎信息不完整,推测补充了“秀丽隐杆线虫”以使句子完整通顺)
G3 (Bethesda). 2018 Jul 2;8(7):2389-2398. doi: 10.1534/g3.118.200360.
3
G Protein-Coupled Receptors as Targets for Approved Drugs: How Many Targets and How Many Drugs?
G 蛋白偶联受体作为已批准药物的靶点:有多少个靶点和多少种药物?
Mol Pharmacol. 2018 Apr;93(4):251-258. doi: 10.1124/mol.117.111062. Epub 2018 Jan 3.
4
G protein-coupled receptor kinases: Past, present and future.G 蛋白偶联受体激酶:过去、现在和未来。
Cell Signal. 2018 Jan;41:17-24. doi: 10.1016/j.cellsig.2017.07.004. Epub 2017 Jul 12.
5
The protein arginine methyltransferase PRMT5 promotes D2-like dopamine receptor signaling.蛋白质精氨酸甲基转移酶PRMT5促进D2样多巴胺受体信号传导。
Sci Signal. 2015 Nov 10;8(402):ra115. doi: 10.1126/scisignal.aad0872.
6
G protein-coupled receptors: abnormalities in signal transmission, disease states and pharmacotherapy.G蛋白偶联受体:信号转导异常、疾病状态与药物治疗
Acta Pol Pharm. 2014 Mar-Apr;71(2):229-43.
7
Defining the RGG/RG motif.定义 RGG/RG 基序。
Mol Cell. 2013 Jun 6;50(5):613-23. doi: 10.1016/j.molcel.2013.05.021.
8
Protein arginine methylation in mammals: who, what, and why.哺乳动物中的蛋白质精氨酸甲基化:何人、何物及为何。
Mol Cell. 2009 Jan 16;33(1):1-13. doi: 10.1016/j.molcel.2008.12.013.
9
Mutant G-protein-coupled receptors as a cause of human diseases.突变型G蛋白偶联受体作为人类疾病的一个病因
Pharmacol Ther. 2004 Dec;104(3):173-206. doi: 10.1016/j.pharmthera.2004.08.008.
10
A proteomic analysis of arginine-methylated protein complexes.精氨酸甲基化蛋白复合物的蛋白质组学分析
Mol Cell Proteomics. 2003 Dec;2(12):1319-30. doi: 10.1074/mcp.M300088-MCP200. Epub 2003 Oct 7.