Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Conservation of Protein Domains Over Different Proteins02:26

Conservation of Protein Domains Over Different Proteins

15.0K
Protein domains are small structurally independent units that are part of a single amino acid chain.  Although these domains are often structurally independent, they may rely on synergistic effects to perform their functions as part of a larger protein. Protein domains may be conserved within the same organism, as well as across different organisms.
A limited set of protein domains often duplicate and recombine during evolution. These domains can be organized in different combinations to...
15.0K
Protein Families02:47

Protein Families

17.5K
Protein families are groups of homologous proteins; that is, they have similarities in amino acid sequences and three-dimensional structures. Protein families usually occur because of gene duplication, where an additional copy of a gene is inserted into the genome of an organism.   Mutations that change the amino acids but still allow the protein to be properly synthesized, will lead to new protein family members.   If these new proteins contain similar amino acids in key...
17.5K
Protein Complexes with Interchangeable Parts01:57

Protein Complexes with Interchangeable Parts

3.1K
Groups of proteins may form a complex where each protein in this complex has a different role in the overall execution of the complex’s function. Often some of the proteins in the complex can be replaced by a closely related variant to give a complex that contains many of the same components yet is functionally distinct.
The SCF ubiquitin ligase is a protein complex of five individual proteins. This complex attaches ubiquitin to other target proteins to mark them for degradation. In order...
3.1K
Protein Complexes with Interchangeable Parts01:57

Protein Complexes with Interchangeable Parts

2.2K
2.2K
Intrinsically Disordered Proteins02:18

Intrinsically Disordered Proteins

21.6K
Intrinsically disordered proteins are a group of proteins that do not fold into specific three-dimensional structures. Their structural flexibility allows them to complement ordered proteins to perform functions that are inaccessible to rigid structures. They are more common in eukaryotes than prokaryotes and may either be exclusively intrinsically disordered or hybrid proteins, consisting of a mix of ordered and disordered regions. The absence of a rigid structure in these proteins can be...
21.6K
Intrinsically Disordered Proteins02:18

Intrinsically Disordered Proteins

3.0K
3.0K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Interactions of outer membrane lipoproteins <i>P. aeruginosa</i> PA3214 and <i>E. coli</i> PqiC with their MCE protein binding partners, PA3213 and PqiB.

bioRxiv : the preprint server for biology·2026
Same author

Ultrastructural insights into the polar tube invasion organelle from microsporidian parasites.

Current opinion in microbiology·2026
Same author

LetA defines a structurally distinct transporter family.

Nature·2026
Same author

Bond-centric modular design of protein assemblies.

Nature materials·2025
Same author

scRNA-seq uncovers the transcriptional dynamics of Encephalitozoon intestinalis parasites in human macrophages.

Nature communications·2025
Same author

LetA defines a structurally distinct transporter family involved in lipid trafficking.

bioRxiv : the preprint server for biology·2025

相关实验视频

Updated: Mar 28, 2026

Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
10:58

Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules

Published on: July 25, 2013

17.7K

通过计算蛋白质设计探索重复蛋白质宇宙

T J Brunette1,2, Fabio Parmeggiani1,2, Po-Ssu Huang1,2

  • 1Department of Biochemistry, University of Washington, Seattle, Washington 98195, USA.

Nature
|December 18, 2015
PubMed
概括

科学家们通过设计新的重复蛋白质来探索蛋白质结构的巨大潜力. 他们的研究表明,大自然只使用了可能的蛋白质设计的一小部分,

更多相关视频

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues
07:08

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues

Published on: July 14, 2015

7.8K
Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
05:08

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins

Published on: July 8, 2025

1.3K

相关实验视频

Last Updated: Mar 28, 2026

Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
10:58

Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules

Published on: July 25, 2013

17.7K
Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues
07:08

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues

Published on: July 14, 2015

7.8K
Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins
05:08

Application of I TASSER, trRosetta, UCSF Chimera, HADDOCK server, and HEX loria for De Novo and In Silico Design of Proteins

Published on: July 8, 2025

1.3K

科学领域:

  • 结构生物学
  • 计算式蛋白质设计
  • 蛋白质的演变

背景情况:

  • 重复蛋白对于分子识别和信号传递等生物过程至关重要.
  • 自然存在的重复蛋白质已经被设计为各种应用.
  • 了解各种可能的蛋白质结构是蛋白质进化的关键问题.

研究的目的:

  • 通过重复一个简单的螺旋环-螺旋环模式来研究可实现的结构多样性.
  • 确定新的重复蛋白质结构是否可以通过计算设计和实验验证.
  • 在自然发生的例子之外探索重复蛋白的序列和结构空间.

主要方法:

  • 使用计算式蛋白质设计生成新的重复蛋白质序列.
  • 通过计算设计的83种蛋白质进行了合成和实验性表征.
  • 技术包括评估蛋白质稳定性,溶液X射线散射和晶体结构的确定.

主要成果:

  • 其中53个设计是单质的,在95°C稳定.
  • 43个设计显示了与它们预测的结构一致的溶液X射线散射光谱.
  • 15个设计的晶体结构与计算模型密切一致,RMSD从0.7到2.5 Å.

结论:

  • 现有的重复蛋白代表了潜在的序列和结构空间的小子集.
  • 可以通过计算设计具有特定几何形状的新型重复蛋白.
  • 这项工作扩大了生物分子工程和蛋白质设计的可能性.