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相关概念视频

Mismatch Repair01:36

Mismatch Repair

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Overview of DNA Repair02:25

Overview of DNA Repair

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In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
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Mutations01:39

Mutations

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Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
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Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

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Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
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相关实验视频

Updated: Jun 3, 2025

Following the Dynamics of Structural Variants in Experimentally Evolved Populations
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Following the Dynamics of Structural Variants in Experimentally Evolved Populations

Published on: February 3, 2023

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关于稳定内部突变的结构和能量分析.

Yulia M Gutierrez1,2,3, Gabriel J Rocklin1,2,3

  • 1Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL.

bioRxiv : the preprint server for biology
|January 7, 2025
PubMed
概括

氨基酸插入和删除 (indels) 可以惊人地增加蛋白质的稳定性. 计算分析显示,这些突变往往具有局部效应,并且可以通过能量函数比反向折叠模型更好地预测.

科学领域:

  • 蛋白质的生物化学 蛋白质的生物化学
  • 计算生物学是一种计算生物学.
  • 结构生物学是结构生物学.

背景情况:

  • 氨基酸插入和删除 (indels) 是影响蛋白质结构的常见突变.
  • 了解indels如何影响蛋白质折叠的稳定性对于蛋白质工程至关重要.

研究的目的:

  • 通过计算分析稳定体内突变的结构和能量影响.
  • 评估不同计算模型对蛋白质稳定性的预测能力.

主要方法:

  • 对103个经过实验识别的稳定单氨基酸indel突变物的分析.
  • 利用计算建模来评估结构和能量变化.
  • 罗塞塔的能量函数和一个反向折叠 (ESM-IF) 模型的比较预测.

主要成果:

  • 稳定性体通常会导致局部结构变化.
  • 稳定删除,而不是插入,往往位于紧张的脊椎区域.
  • 罗塞塔的能量函数准确地分类了稳定性,而ESM-IF则没有.

结论:

  • 脊柱能源在印度的稳定作用中发挥着重要作用.

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  • 专注于明确的骨干能量学的计算模型更有效地预测稳定indel突变.
  • 这些发现可以为蛋白质工程和稳定性增强的新策略提供信息.