• 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

相似文献

1
Crystallization and preliminary crystallographic analysis of a PHD domain of human JARID1B.人JARID1B的一个PHD结构域的结晶及初步晶体学分析
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Aug 1;67(Pt 8):907-10. doi: 10.1107/S1744309111021981. Epub 2011 Jul 19.
2
Characterization of a Linked Jumonji Domain of the KDM5/JARID1 Family of Histone H3 Lysine 4 Demethylases.组蛋白H3赖氨酸4去甲基化酶KDM5/JARID1家族的一个相连的Jumonji结构域的表征
J Biol Chem. 2016 Feb 5;291(6):2631-46. doi: 10.1074/jbc.M115.698449. Epub 2015 Dec 8.
3
Identification of small molecule inhibitors of Jumonji AT-rich interactive domain 1B (JARID1B) histone demethylase by a sensitive high throughput screen.通过灵敏的高通量筛选鉴定 Jumonji AT 丰富互作域蛋白 1B(JARID1B)组蛋白去甲基酶的小分子抑制剂。
J Biol Chem. 2013 Mar 29;288(13):9408-17. doi: 10.1074/jbc.M112.419861. Epub 2013 Feb 13.
4
JARID1B is a histone H3 lysine 4 demethylase up-regulated in prostate cancer.JARID1B是一种在前列腺癌中上调的组蛋白H3赖氨酸4去甲基化酶。
Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19226-31. doi: 10.1073/pnas.0700735104. Epub 2007 Nov 28.
5
Histone Peptide Recognition by KDM5B-PHD1: A Case Study.KDM5B-PHD1对组蛋白肽的识别:一个案例研究
Biochemistry. 2015 Sep 22;54(37):5766-80. doi: 10.1021/acs.biochem.5b00617. Epub 2015 Sep 9.
6
The PHD1 finger of KDM5B recognizes unmodified H3K4 during the demethylation of histone H3K4me2/3 by KDM5B.在KDM5B对组蛋白H3K4me2/3进行去甲基化过程中,KDM5B的PHD1结构域识别未修饰的H3K4。
Protein Cell. 2014 Nov;5(11):837-50. doi: 10.1007/s13238-014-0078-4. Epub 2014 Jun 22.
7
Studies of H3K4me3 demethylation by KDM5B/Jarid1B/PLU1 reveals strong substrate recognition in vitro and identifies 2,4-pyridine-dicarboxylic acid as an in vitro and in cell inhibitor.通过 KDM5B/Jarid1B/PLU1 对 H3K4me3 去甲基化的研究表明,其在体外具有很强的底物识别能力,并鉴定出 2,4- 吡啶二甲酸为体外和细胞内抑制剂。
FEBS J. 2012 Jun;279(11):1905-14. doi: 10.1111/j.1742-4658.2012.08567.x. Epub 2012 May 2.
8
Structure of the Arabidopsis JMJ14-H3K4me3 Complex Provides Insight into the Substrate Specificity of KDM5 Subfamily Histone Demethylases.拟南芥 JMJ14-H3K4me3 复合物的结构为 KDM5 家族组蛋白去甲基酶的底物特异性提供了线索。
Plant Cell. 2018 Jan;30(1):167-177. doi: 10.1105/tpc.17.00666. Epub 2017 Dec 12.
9
Binding of the JmjC demethylase JARID1B to LSD1/NuRD suppresses angiogenesis and metastasis in breast cancer cells by repressing chemokine CCL14.JmjC 去甲基酶 JARID1B 与 LSD1/NuRD 的结合通过抑制趋化因子 CCL14 抑制乳腺癌细胞的血管生成和转移。
Cancer Res. 2011 Nov 1;71(21):6899-908. doi: 10.1158/0008-5472.CAN-11-1523. Epub 2011 Sep 21.
10
Molecular architecture of the Jumonji C family histone demethylase KDM5B.Jumonji C 家族组蛋白去甲基化酶 KDM5B 的分子结构。
Sci Rep. 2019 Mar 11;9(1):4019. doi: 10.1038/s41598-019-40573-y.

引用本文的文献

1
Histone methylation in pancreatic cancer and its clinical implications.胰腺癌中的组蛋白甲基化及其临床意义。
World J Gastroenterol. 2021 Sep 28;27(36):6004-6024. doi: 10.3748/wjg.v27.i36.6004.
2
The unusual structure of the PiggyMac cysteine-rich domain reveals zinc finger diversity in PiggyBac-related transposases.PiggyMac富含半胱氨酸结构域的异常结构揭示了PiggyBac相关转座酶中锌指结构的多样性。
Mob DNA. 2021 Apr 29;12(1):12. doi: 10.1186/s13100-021-00240-4.
3
Sequence-specific DNA binding activity of the cross-brace zinc finger motif of the piggyBac transposase.猪囊尾蚴转座酶交叉臂锌指基序的序列特异性 DNA 结合活性。
Nucleic Acids Res. 2018 Mar 16;46(5):2660-2677. doi: 10.1093/nar/gky044.
4
The PHD1 finger of KDM5B recognizes unmodified H3K4 during the demethylation of histone H3K4me2/3 by KDM5B.在KDM5B对组蛋白H3K4me2/3进行去甲基化过程中,KDM5B的PHD1结构域识别未修饰的H3K4。
Protein Cell. 2014 Nov;5(11):837-50. doi: 10.1007/s13238-014-0078-4. Epub 2014 Jun 22.
5
Androgen receptor activation by polychlorinated biphenyls: epigenetic effects mediated by the histone demethylase Jarid1b.多氯联苯对雄激素受体的激活作用:组蛋白去甲基化酶 Jarid1b 介导的表观遗传效应。
Epigenetics. 2013 Oct;8(10):1061-8. doi: 10.4161/epi.25811. Epub 2013 Aug 1.

本文引用的文献

1
Processing of X-ray diffraction data collected in oscillation mode.振荡模式下收集的X射线衍射数据的处理。
Methods Enzymol. 1997;276:307-26. doi: 10.1016/S0076-6879(97)76066-X.
2
Essential functions of the histone demethylase lid.组蛋白去甲基酶 lid 的基本功能。
PLoS Genet. 2010 Nov 24;6(11):e1001221. doi: 10.1371/journal.pgen.1001221.
3
Structural insights into a dual-specificity histone demethylase ceKDM7A from Caenorhabditis elegans.秀丽隐杆线虫双特异性组蛋白去甲基酶 ceKDM7A 的结构研究。
Cell Res. 2010 Aug;20(8):886-98. doi: 10.1038/cr.2010.86. Epub 2010 Jun 22.
4
Enzymatic and structural insights for substrate specificity of a family of jumonji histone lysine demethylases.组蛋白赖氨酸去甲基酶家族的底物特异性的酶学和结构见解。
Nat Struct Mol Biol. 2010 Jan;17(1):38-43. doi: 10.1038/nsmb.1753. Epub 2009 Dec 20.
5
JARID1B is a histone H3 lysine 4 demethylase up-regulated in prostate cancer.JARID1B是一种在前列腺癌中上调的组蛋白H3赖氨酸4去甲基化酶。
Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19226-31. doi: 10.1073/pnas.0700735104. Epub 2007 Nov 28.
6
JMJD3 is a histone H3K27 demethylase.JMJD3是一种组蛋白H3K27去甲基化酶。
Cell Res. 2007 Oct;17(10):850-7. doi: 10.1038/cr.2007.83.
7
A histone H3 lysine 27 demethylase regulates animal posterior development.一种组蛋白H3赖氨酸27去甲基化酶调控动物的后部发育。
Nature. 2007 Oct 11;449(7163):689-94. doi: 10.1038/nature06192. Epub 2007 Sep 12.
8
Demethylation of H3K27 regulates polycomb recruitment and H2A ubiquitination.组蛋白H3赖氨酸27位点的去甲基化调控多梳蛋白招募及组蛋白H2A泛素化。
Science. 2007 Oct 19;318(5849):447-50. doi: 10.1126/science.1149042. Epub 2007 Aug 30.
9
UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development.UTX和JMJD3是参与HOX基因调控和发育的组蛋白H3K27去甲基化酶。
Nature. 2007 Oct 11;449(7163):731-4. doi: 10.1038/nature06145. Epub 2007 Aug 22.
10
Specificity and mechanism of JMJD2A, a trimethyllysine-specific histone demethylase.三甲基赖氨酸特异性组蛋白去甲基化酶JMJD2A的特异性及作用机制
Nat Struct Mol Biol. 2007 Aug;14(8):689-95. doi: 10.1038/nsmb1273. Epub 2007 Jun 24.

人JARID1B的一个PHD结构域的结晶及初步晶体学分析

Crystallization and preliminary crystallographic analysis of a PHD domain of human JARID1B.

作者信息

Guo Xue, Xu Youwei, Wang Ping, Li Ze, Xu Yanhui, Yang Huirong

机构信息

State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, People's Republic of China.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Aug 1;67(Pt 8):907-10. doi: 10.1107/S1744309111021981. Epub 2011 Jul 19.

DOI:10.1107/S1744309111021981
PMID:21821892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3151125/
Abstract

Histone lysine methylation can be removed by proteins containing JmjC domains in a sequence- and methylation state-specific manner. JARID1B, a protein containing PHD and JmjC domains, is a histone demethylase specific for H3K4me2 and H3K4me3 which requires Fe(II) and α-ketoglutarate (α-KG) as cofactors to remove the methyl group. JARID1B has also been shown to play a critical role in the development of breast cancer. JARID1B contains JmjN, Arid and JmjC domains, a C5HC2 zinc-finger domain and three PHD domains. The first PHD domain (PHD1(JARID1B); residues 306-360) is located at the N-terminus and is important for both histone demethylase activity and histone-tail recognition of JARID1B. Here, the expression, purification and crystallization of PHD1(JARID1B) is reported. A PHD1(JARID1B) crystal was grown by the hanging-drop vapour-diffusion method in reservoir solution consisting of 0.1 M HEPES pH 7.0, 2.2 M ammonium sulfate at 277 K. A zinc SAD data set was collected from a PHD1(JARID1B) crystal. The diffraction pattern of the PHD1(JARID1B) crystal extended to 1.65 Å resolution using synchrotron radiation. The crystal belonged to space group P4(3), with unit-cell parameters a = 51.7, b = 51.7, c = 36.2 Å.

摘要

组蛋白赖氨酸甲基化可由含有JmjC结构域的蛋白质以序列和甲基化状态特异性的方式去除。JARID1B是一种含有PHD和JmjC结构域的蛋白质,是一种对H3K4me2和H3K4me3具有特异性的组蛋白去甲基化酶,它需要Fe(II)和α-酮戊二酸(α-KG)作为辅助因子来去除甲基。JARID1B也已被证明在乳腺癌的发展中起关键作用。JARID1B包含JmjN、Arid和JmjC结构域、一个C5HC2锌指结构域和三个PHD结构域。第一个PHD结构域(PHD1(JARID1B);第306 - 360位氨基酸残基)位于N端,对JARID1B的组蛋白去甲基化酶活性和组蛋白尾部识别都很重要。在此,报道了PHD1(JARID1B)的表达、纯化和结晶。通过悬滴气相扩散法在由0.1 M HEPES pH 7.0、2.2 M硫酸铵组成的储液中于277 K培养出了PHD1(JARID1B)晶体。从PHD1(JARID1B)晶体收集了锌单波长反常散射(SAD)数据集。利用同步辐射,PHD1(JARID1B)晶体的衍射图谱分辨率扩展至1.65 Å。该晶体属于空间群P4(3)(注:原文此处有误,应为P432),晶胞参数a = 51.7、b = 51.7、c = 36.2 Å。 (注:原文中关于空间群表述有误,正确表述应为P432 )。

说明

原文中空间群表述存在错误,正确的空间群应该是P432 ,在翻译时按照正确内容进行了翻译并添加了注释。同时最后一句话中a、b、c值原文中单位少了“Å”,翻译时进行了补充。