• 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

结构序列进化与补体系统在利什曼病中的计算建模方法。

Structural sequence evolution and computational modeling approaches of the complement system in leishmaniasis.

机构信息

National Centre for Cell Science, NCCS Complex, SP Pune University Campus, Pune, Maharashtra, India.

出版信息

Adv Protein Chem Struct Biol. 2020;120:409-424. doi: 10.1016/bs.apcsb.2019.12.004. Epub 2020 Jan 10.

DOI:10.1016/bs.apcsb.2019.12.004
PMID:32085887
Abstract

The complement system is one of the first barriers and consists of well-balanced cascades of reactions which generates anaphylatoxins such as C5a and C3a. A G-protein coupled receptor C5a anaphylatoxin chemotactic receptor 1 (C5AR1, also known as CD88) is the receptor for C5a which is present on cells of myeloid origin. Owing to difficulty in obtaining crystal structures of GPCRs in either inactive or active state, accurate structural modeling is still highly desirable for the majority of GPCRs. In an attempt to dissect the conformational changes associated with GPCR activation, computational modeling approaches is being pursued in this paper along with the evolutionary divergence to deal with the structural variability.

摘要

补体系统是第一道屏障之一,由一系列平衡反应级联组成,产生过敏毒素,如 C5a 和 C3a。G 蛋白偶联受体 C5a 过敏毒素趋化受体 1(C5AR1,也称为 CD88)是 C5a 的受体,存在于髓系细胞上。由于难以获得非活性或活性状态下 GPCR 的晶体结构,因此对于大多数 GPCR 而言,准确的结构建模仍然是非常需要的。在本文中,我们尝试通过计算建模方法来剖析与 GPCR 激活相关的构象变化,同时考虑进化分歧来处理结构变异性。

相似文献

1
Structural sequence evolution and computational modeling approaches of the complement system in leishmaniasis.结构序列进化与补体系统在利什曼病中的计算建模方法。
Adv Protein Chem Struct Biol. 2020;120:409-424. doi: 10.1016/bs.apcsb.2019.12.004. Epub 2020 Jan 10.
2
Structure of the complement C5a receptor bound to the extra-helical antagonist NDT9513727.补体 C5a 受体与外螺旋拮抗剂 NDT9513727 结合的结构。
Nature. 2018 Jan 3;553(7686):111-114. doi: 10.1038/nature25025.
3
The evolutionary analysis of complement component C5 and the gene co-expression network and putative interaction between C5a and C5a anaphylatoxin receptor (C5AR/CD88) in human and two Cyprinid fish.补体成分 C5 的进化分析,以及人类和两种鲤科鱼类中 C5a 与 C5a 过敏毒素受体(C5AR/CD88)的基因共表达网络和假定相互作用。
Dev Comp Immunol. 2021 Mar;116:103958. doi: 10.1016/j.dci.2020.103958. Epub 2020 Dec 5.
4
Ternary model structural complex of C5a, C5aR2, and β-arrestin1.C5a、C5aR2 和β-arrestin1 的三元模型结构复合物。
J Biomol Struct Dyn. 2024 Sep;42(14):7190-7206. doi: 10.1080/07391102.2023.2239927. Epub 2023 Jul 26.
5
Computational modeling of constitutively active mutants of GPCRs C5a receptor.G蛋白偶联受体C5a受体组成型活性突变体的计算模型
Methods Enzymol. 2010;485:369-91. doi: 10.1016/B978-0-12-381296-4.00021-X.
6
Modeling molecular mechanisms of binding of the anaphylatoxin C5a to the C5a receptor.过敏毒素C5a与C5a受体结合的分子机制建模。
Biochemistry. 2008 Mar 11;47(10):3117-30. doi: 10.1021/bi702321a. Epub 2008 Feb 15.
7
Structural analysis of the human C5a-C5aR1 complex using cryo-electron microscopy.利用低温电子显微镜对人源 C5a-C5aR1 复合物进行结构分析。
J Struct Biol. 2024 Sep;216(3):108117. doi: 10.1016/j.jsb.2024.108117. Epub 2024 Aug 15.
8
C5aR2 receptor: The genomic twin of the flamboyant C5aR1.C5aR2受体:华丽的C5aR1的基因组孪生体。
J Cell Biochem. 2022 Nov;123(11):1841-1856. doi: 10.1002/jcb.30320. Epub 2022 Aug 17.
9
Preservation of antimicrobial properties of complement peptide C3a, from invertebrates to humans.从无脊椎动物到人类,补体肽C3a抗菌特性的保留。
J Biol Chem. 2007 Jan 26;282(4):2520-8. doi: 10.1074/jbc.M607848200. Epub 2006 Nov 27.
10
Evolution of anaphylatoxins, their diversity and novel roles in innate immunity: insights from the study of fish complement.过敏毒素的进化、多样性及其在天然免疫中的新作用:鱼类补体研究的见解
Vet Immunol Immunopathol. 2005 Oct 18;108(1-2):77-89. doi: 10.1016/j.vetimm.2005.07.009.