• 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

假 GTPase 组的假酶。

The pseudoGTPase group of pseudoenzymes.

机构信息

Department of Pharmacology, Yale University, New Haven, CT, USA.

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.

出版信息

FEBS J. 2020 Oct;287(19):4232-4245. doi: 10.1111/febs.15554. Epub 2020 Sep 17.

DOI:10.1111/febs.15554
PMID:32893973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7544640/
Abstract

Pseudoenzymes are emerging as significant mediators and regulators of signal transduction. These proteins maintain enzyme folds and topologies, but are disrupted in the conserved motifs required for enzymatic activity. Among the pseudoenzymes, the pseudoGTPase group of atypical GTPases has recently expanded and includes the Rnd and RGK groups, RhoH and the RhoBTB proteins, mitochondrial RhoGTPase and centaurin-γ groups, CENP-M, dynein LIC, Entamoeba histolytica RabX3, leucine-rich repeat kinase 2, and the p190RhoGAP proteins. The wide range of cellular functions associated with pseudoGTPases includes cell migration and adhesion, membrane trafficking and cargo transport, mitosis, mitochondrial activity, transcriptional control, and autophagy, placing the group in an expanding portfolio of signaling pathways. In this review, we examine how the pseudoGTPases differ from canonical GTPases and consider their mechanistic and functional roles in signal transduction. We review the amino acid differences between the pseudoGTPases and discuss how these proteins can be classified based on their ability to bind nucleotide and their enzymatic activity. We discuss the molecular and structural consequences of amino acid divergence from canonical GTPases and use comparison with the well-studied pseudokinases to illustrate the classifications. PseudoGTPases are fast becoming recognized as important mechanistic components in a range of cellular roles, and we provide a concise discussion of the currently identified members of this group. ENZYMES: small GTPases; EC number: EC 3.6.5.2.

摘要

拟酶正在成为信号转导的重要介质和调节剂。这些蛋白质保持酶的折叠和拓扑结构,但在酶活性所必需的保守基序中被破坏。在拟酶中,非典型 GTP 酶的拟 GTPase 组最近扩大,包括 Rnd 和 RGK 组、RhoH 和 RhoBTB 蛋白、线粒体 RhoGTPase 和 centaurin-γ 组、CENP-M、动力蛋白 LIC、溶组织内阿米巴 RabX3、富含亮氨酸重复激酶 2 和 p190RhoGAP 蛋白。与拟 GTPase 相关的广泛的细胞功能包括细胞迁移和黏附、膜运输和货物运输、有丝分裂、线粒体活性、转录控制和自噬,使该组处于不断扩大的信号通路组合中。在这篇综述中,我们研究了拟 GTPase 与典型 GTPase 的区别,并考虑了它们在信号转导中的机制和功能作用。我们审查了拟 GTPase 与典型 GTPase 之间的氨基酸差异,并讨论了如何根据它们结合核苷酸的能力和酶活性对这些蛋白质进行分类。我们讨论了与典型 GTPase 氨基酸差异的分子和结构后果,并使用与研究充分的假激酶的比较来说明分类。拟 GTPase 正在迅速被认为是一系列细胞功能中的重要机制成分,我们对这一组目前已确定的成员进行了简洁的讨论。ENZYMES: small GTPases; EC number: EC 3.6.5.2.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/c19a3cf31a5a/nihms-1630678-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/5eed58b64951/nihms-1630678-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/afe5dae46377/nihms-1630678-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/c19a3cf31a5a/nihms-1630678-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/5eed58b64951/nihms-1630678-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/afe5dae46377/nihms-1630678-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb6/7544640/c19a3cf31a5a/nihms-1630678-f0003.jpg

相似文献

1
The pseudoGTPase group of pseudoenzymes.假 GTPase 组的假酶。
FEBS J. 2020 Oct;287(19):4232-4245. doi: 10.1111/febs.15554. Epub 2020 Sep 17.
2
PseudoGTPase domains in p190RhoGAP proteins: a mini-review.p190RhoGAP 蛋白中的假 GTP 酶结构域:小型综述。
Biochem Soc Trans. 2018 Dec 17;46(6):1713-1720. doi: 10.1042/BST20180481. Epub 2018 Dec 4.
3
The N-Terminal GTPase Domain of p190RhoGAP Proteins Is a PseudoGTPase.p190RhoGAP 蛋白的 N 端 GTP 酶结构域是一种假 GTP 酶。
Structure. 2018 Nov 6;26(11):1451-1461.e4. doi: 10.1016/j.str.2018.07.015. Epub 2018 Aug 30.
4
p190RhoGAP proteins contain pseudoGTPase domains.p190RhoGAP蛋白含有假GTP酶结构域。
Nat Commun. 2017 Sep 11;8(1):506. doi: 10.1038/s41467-017-00483-x.
5
Atypical GTPases as drug targets.非典型 GTP 酶作为药物靶点。
Anticancer Agents Med Chem. 2012 Jan;12(1):19-28. doi: 10.2174/187152012798764705.
6
Emerging concepts in pseudoenzyme classification, evolution, and signaling.伪酶分类、进化和信号转导的新观点。
Sci Signal. 2019 Aug 13;12(594):eaat9797. doi: 10.1126/scisignal.aat9797.
7
Classification and evolution of P-loop GTPases and related ATPases.P 环鸟苷三磷酸酶及相关腺苷三磷酸酶的分类与进化
J Mol Biol. 2002 Mar 15;317(1):41-72. doi: 10.1006/jmbi.2001.5378.
8
The hematopoiesis-specific GTP-binding protein RhoH is GTPase deficient and modulates activities of other Rho GTPases by an inhibitory function.造血特异性GTP结合蛋白RhoH缺乏GTP酶活性,并通过抑制功能调节其他Rho GTP酶的活性。
Mol Cell Biol. 2002 Feb;22(4):1158-71. doi: 10.1128/MCB.22.4.1158-1171.2002.
9
Emerging functions of pseudoenzymes.伪酶的新兴功能。
Biochem J. 2023 May 31;480(10):715-728. doi: 10.1042/BCJ20220373.
10
Live and let die: insights into pseudoenzyme mechanisms from structure.生死由命:从结构角度洞察假酶机制。
Curr Opin Struct Biol. 2017 Dec;47:95-104. doi: 10.1016/j.sbi.2017.07.004. Epub 2017 Aug 5.

引用本文的文献

1
Interface integrity in septin protofilaments is maintained by an arginine residue conserved from yeast to man.Septins原丝中的界面完整性由一个从酵母到人类都保守的精氨酸残基维持。
Mol Biol Cell. 2025 May 1;36(5):ar59. doi: 10.1091/mbc.E25-01-0041. Epub 2025 Mar 26.
2
The small GTPase MRAS is a broken switch.小GTP酶MRAS是一个失灵的开关。
Nat Commun. 2025 Jan 14;16(1):647. doi: 10.1038/s41467-025-55967-y.
3
Gene Expression Dysregulation in Whole Blood of Patients with Infection.感染患者全血中的基因表达失调

本文引用的文献

1
The In Situ Structure of Parkinson's Disease-Linked LRRK2.帕金森病相关 LRRK2 的原位结构。
Cell. 2020 Sep 17;182(6):1508-1518.e16. doi: 10.1016/j.cell.2020.08.004. Epub 2020 Aug 11.
2
Miro: A molecular switch at the center of mitochondrial regulation.Miro:线粒体调控中心的分子开关。
Protein Sci. 2020 Jun;29(6):1269-1284. doi: 10.1002/pro.3839. Epub 2020 Feb 24.
3
Cataloguing the dead: breathing new life into pseudokinase research.为死者立传:为假激酶研究注入新活力。
Int J Mol Sci. 2024 Nov 25;25(23):12653. doi: 10.3390/ijms252312653.
4
Complex interplay between RAS GTPases and RASSF effectors regulates subcellular localization of YAP.RAS GTPases 与 RASSF 效应物之间的复杂相互作用调节 YAP 的亚细胞定位。
EMBO Rep. 2024 Aug;25(8):3574-3600. doi: 10.1038/s44319-024-00203-9. Epub 2024 Jul 15.
5
Rem2 interacts with CaMKII at synapses and restricts long-term potentiation in hippocampus.Rem2 在突触处与 CaMKII 相互作用,限制海马体中的长时程增强。
PLoS One. 2024 Jul 12;19(7):e0301063. doi: 10.1371/journal.pone.0301063. eCollection 2024.
6
A dynamin superfamily-like pseudoenzyme coordinates with MICOS to promote cristae architecture.一种动力蛋白超家族样假酶与 MICOS 协同作用促进嵴结构。
Curr Biol. 2024 Jun 17;34(12):2606-2622.e9. doi: 10.1016/j.cub.2024.04.028. Epub 2024 Apr 30.
7
Rem2 interacts with CaMKII at synapses and restricts long-term potentiation in hippocampus.Rem2在突触处与CaMKII相互作用,并限制海马体中的长时程增强。
bioRxiv. 2024 Mar 12:2024.03.11.584540. doi: 10.1101/2024.03.11.584540.
8
Evolutionary degeneration of septins into pseudoGTPases: impacts on a hetero-oligomeric assembly interface.Septins向假GTP酶的进化退化:对异源寡聚体组装界面的影响。
Front Cell Dev Biol. 2023 Nov 29;11:1296657. doi: 10.3389/fcell.2023.1296657. eCollection 2023.
9
A DRP-like pseudoenzyme coordinates with MICOS to promote cristae architecture.一种类似DRP的假酶与MICOS协同作用以促进嵴结构的形成。
bioRxiv. 2023 Oct 4:2023.10.03.560745. doi: 10.1101/2023.10.03.560745.
10
Obscurin Rho GEF domains are phosphorylated by MST-family kinases but do not exhibit nucleotide exchange factor activity towards Rho GTPases in vitro. obscurin Rho GEF 结构域可被 MST 家族激酶磷酸化,但在体外不表现出针对 Rho GTPases 的核苷酸交换因子活性。
PLoS One. 2023 Apr 20;18(4):e0284453. doi: 10.1371/journal.pone.0284453. eCollection 2023.
FEBS J. 2020 Oct;287(19):4150-4169. doi: 10.1111/febs.15246. Epub 2020 Mar 10.
4
Identifying pseudoenzymes using functional annotation: pitfalls of common practice.利用功能注释识别假酶:常见做法的陷阱。
FEBS J. 2020 Oct;287(19):4128-4140. doi: 10.1111/febs.15142. Epub 2019 Dec 5.
5
Challenges in the annotation of pseudoenzymes in databases: the UniProtKB approach.数据库中假酶注释的挑战:UniProtKB 方法。
FEBS J. 2020 Oct;287(19):4114-4127. doi: 10.1111/febs.15100. Epub 2019 Nov 3.
6
DALI and the persistence of protein shape.DALI 与蛋白质构象的稳定性。
Protein Sci. 2020 Jan;29(1):128-140. doi: 10.1002/pro.3749. Epub 2019 Nov 5.
7
Structure of the dynein-2 complex and its assembly with intraflagellar transport trains.动力蛋白-2 复合物的结构及其与鞭毛内运输列车的组装。
Nat Struct Mol Biol. 2019 Sep;26(9):823-829. doi: 10.1038/s41594-019-0286-y. Epub 2019 Aug 26.
8
Emerging concepts in pseudoenzyme classification, evolution, and signaling.伪酶分类、进化和信号转导的新观点。
Sci Signal. 2019 Aug 13;12(594):eaat9797. doi: 10.1126/scisignal.aat9797.
9
Roco Proteins: GTPases with a Baroque Structure and Mechanism.Roco 蛋白:具有巴洛克结构和机制的 GTPases。
Int J Mol Sci. 2019 Jan 3;20(1):147. doi: 10.3390/ijms20010147.
10
Roco Proteins and the Parkinson's Disease-Associated LRRK2.Roco 蛋白与帕金森病相关的 LRRK2
Int J Mol Sci. 2018 Dec 17;19(12):4074. doi: 10.3390/ijms19124074.