Expansion and Further Development of the PSIPRED Protein Structure and Function Bioinformatics Workbench
PSIPRED 蛋白质结构和功能生物信息学工作台的扩展和进一步发展
基本信息
- 批准号:BB/M011712/1
- 负责人:
- 金额:$ 53.24万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2015
- 资助国家:英国
- 起止时间:2015 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
With many genomes now completely sequenced, life scientists now face the challenge of characterizing the biological role of the encoded proteins as to advance our understanding of cell physiology. Most genes are designed to code for proteins which have useful functions in an organism. Proteins are essentially strings of simpler molecules, called amino acids and these strings can self-assemble into a complex 3-D structure as soon as the protein is formed by the protein-making machinery (ribosomes) in the cell. It is this unique structure which determines the precise chemical function of the protein (i.e. what is does in the cell and how it does it). By firing X-rays at crystallised proteins, scientists can determine their structure, but this process can take many months or even years. With hundreds of thousands of proteins for which the native structure is unknown, it is not surprising that scientists want to find a clever shortcut to working out the structure of proteins. We, like many other scientists have been trying to "crack the code" of protein structure i.e. working out the rules which govern how the protein finds its unique structure and then trying to program a computer with these rules to allow scientists to quickly "predict" what the structure of their protein of interest might be.The PSIPRED Workbench is a collection of Web servers maintained at UCL which does just this i.e. it allows biologists to predict the structure of their protein structure given just its amino acid sequence. Over the years it has helped many thousands of scientists with their work by providing these services and we now wish not only to upgrade and maintain these existing servers but also to implement new methods which allow the structures of even the most difficult proteins to be deduced by computer simulations.More recently, however, PSIPRED has been given a wider range of features to cover other important problems in biology. For example, using PSIPRED, a scientist can predict which proteins do not fold into stable shapes (called disordered proteins) or which chemical substances are likely to bind to a protein. Even where a protein does not appear to fold into a single stable structure, PSIPRED can still help scientists deduce what the function of his or her protein is likely to be. Generating such information on a large scale using computer algorithms can help expand our knowledge base of the biological role of proteins at a cellular level, and such understanding will be a key stepping stone in the development of techniques and pharmaceuticals to target diseased genes and their products as well as proteins from pathological organisms such as bacteria or viruses. In a similar way, knowledge on the function of certain bacterial genes can, for example, help develop new industrial processes by modifying the genes to make them produce novel chemical compounds, or even helping to detoxify industrial waste by producing friendly bacteria that can use the poisonous chemicals as food.
随着许多基因组的完全测序,生命科学家现在面临的挑战是描述编码蛋白质的生物学作用,以促进我们对细胞生理学的理解。大多数基因被设计为编码在生物体中具有有用功能的蛋白质。蛋白质本质上是一串更简单的分子,称为氨基酸,一旦蛋白质被细胞中的蛋白质制造机制(核糖体)形成,这些分子串就可以自组装成复杂的3-D结构。正是这种独特的结构决定了蛋白质的精确化学功能(即它在细胞中做什么以及如何做)。通过向结晶蛋白质发射x射线,科学家可以确定它们的结构,但这个过程可能需要数月甚至数年的时间。由于有成千上万种蛋白质的天然结构是未知的,所以科学家们想要找到一种聪明的捷径来研究蛋白质的结构也就不足为奇了。像许多其他科学家一样,我们一直在试图“破解”蛋白质结构的密码,即找出控制蛋白质如何找到其独特结构的规则,然后尝试用这些规则编程计算机,使科学家能够快速“预测”他们感兴趣的蛋白质的结构可能是什么。PSIPRED工作台是伦敦大学学院维护的Web服务器的集合,它就是这样做的,即它允许生物学家预测其蛋白质结构的结构,只要它的氨基酸序列。多年来,它通过提供这些服务帮助了成千上万的科学家进行他们的工作,我们现在不仅希望升级和维护这些现有的服务器,而且希望实现新的方法,使即使是最困难的蛋白质的结构也能通过计算机模拟推断出来。然而,最近PSIPRED被赋予了更广泛的特征,以涵盖生物学中的其他重要问题。例如,利用PSIPRED,科学家可以预测哪些蛋白质不能折叠成稳定的形状(称为无序蛋白质),或者哪些化学物质可能与蛋白质结合。即使蛋白质没有折叠成单一的稳定结构,PSIPRED仍然可以帮助科学家推断出他或她的蛋白质的功能可能是什么。使用计算机算法大规模地生成此类信息可以帮助我们扩展蛋白质在细胞水平上的生物学作用的知识库,并且这种理解将是开发针对患病基因及其产物以及来自病理生物体(如细菌或病毒)的蛋白质的技术和药物的关键垫脚石。类似地,对某些细菌基因功能的了解可以,例如,通过修改基因使其产生新的化合物来帮助开发新的工业过程,甚至可以通过产生可以将有毒化学物质作为食物的友好细菌来帮助解毒工业废物。
项目成果
期刊论文数量(8)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Predictions of Backbone Dynamics in Intrinsically Disordered Proteins Using De Novo Fragment-Based Protein Structure Predictions.
- DOI:10.1038/s41598-017-07156-1
- 发表时间:2017-08-01
- 期刊:
- 影响因子:4.6
- 作者:Kosciolek T;Buchan DWA;Jones DT
- 通讯作者:Jones DT
Improved protein contact predictions with the MetaPSICOV2 server in CASP12.
- DOI:10.1002/prot.25379
- 发表时间:2018-03
- 期刊:
- 影响因子:2.9
- 作者:Buchan DWA;Jones DT
- 通讯作者:Jones DT
Design of metalloproteins and novel protein folds using variational autoencoders.
- DOI:10.1038/s41598-018-34533-1
- 发表时间:2018-11-01
- 期刊:
- 影响因子:4.6
- 作者:Greener JG;Moffat L;Jones DT
- 通讯作者:Jones DT
EigenTHREADER: analogous protein fold recognition by efficient contact map threading.
- DOI:10.1093/bioinformatics/btx217
- 发表时间:2017-09-01
- 期刊:
- 影响因子:0
- 作者:Buchan DWA;Jones DT
- 通讯作者:Jones DT
Design of metalloproteins and novel protein folds using variational autoencoders
使用变分自动编码器设计金属蛋白和新型蛋白质折叠
- DOI:10.48550/arxiv.1806.09900
- 发表时间:2018
- 期刊:
- 影响因子:0
- 作者:Greener J
- 通讯作者:Greener J
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David Jones其他文献
Air Toxics Under The Big Sky – A High School Science Teaching Tool
广阔天空下的空气毒物——高中科学教学工具
- DOI:
- 发表时间:
2007 - 期刊:
- 影响因子:0
- 作者:
David Jones;T. Ward;D. Vanek;Nancy Marra;C. Noonan;Garon C. Smith;Earle Adams - 通讯作者:
Earle Adams
Postnatal depression (PND) and neighborhood effects for women enrolled in a home visitation program
参加家访计划的妇女的产后抑郁症 (PND) 和邻里效应
- DOI:
- 发表时间:
2016 - 期刊:
- 影响因子:0
- 作者:
David Jones - 通讯作者:
David Jones
The Effect of Auditory Feedback on the Control of Oral‐Nasal Balance by Pediatric Cochlear Implant Users
听觉反馈对儿童人工耳蜗使用者口鼻平衡控制的影响
- DOI:
10.1097/00003446-199810000-00005 - 发表时间:
1998 - 期刊:
- 影响因子:3.7
- 作者:
M. Svirsky;David Jones;M. Osberger;R. Miyamoto - 通讯作者:
R. Miyamoto
Central Stars of Planetary Nebulae
行星状星云的中心恒星
- DOI:
10.1017/s1743921317000862 - 发表时间:
2016 - 期刊:
- 影响因子:0
- 作者:
David Jones - 通讯作者:
David Jones
David Jones的其他文献
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{{ truncateString('David Jones', 18)}}的其他基金
Open Access Block Award 2024 - The Francis Crick Institute
2024 年开放获取区块奖 - 弗朗西斯·克里克研究所
- 批准号:
EP/Z531844/1 - 财政年份:2024
- 资助金额:
$ 53.24万 - 项目类别:
Research Grant
Open Access Block Award 2023 - The Francis Crick Institute
2023 年开放获取区块奖 - 弗朗西斯·克里克研究所
- 批准号:
EP/Y530360/1 - 财政年份:2023
- 资助金额:
$ 53.24万 - 项目类别:
Research Grant
Open Access Block Award 2022 - The Francis Crick Institute
2022 年开放获取区块奖 - 弗朗西斯·克里克研究所
- 批准号:
EP/X526381/1 - 财政年份:2022
- 资助金额:
$ 53.24万 - 项目类别:
Research Grant
Exploiting Differentiable Programming Models For Protein Structure Prediction And Modelling
利用可微分编程模型进行蛋白质结构预测和建模
- 批准号:
BB/W008556/1 - 财政年份:2022
- 资助金额:
$ 53.24万 - 项目类别:
Research Grant
Accelerating and enhancing the PSIPRED Workbench with deep learning
通过深度学习加速和增强 PSIPRED Workbench
- 批准号:
BB/T019409/1 - 财政年份:2021
- 资助金额:
$ 53.24万 - 项目类别:
Research Grant
Statewide effort to diversify undergraduate engineering student population.
全州范围内努力使本科工程学生群体多样化。
- 批准号:
1848696 - 财政年份:2018
- 资助金额:
$ 53.24万 - 项目类别:
Standard Grant
Cross Disciplinary Thinking about 'Antisocial Personality Disorder'.
关于“反社会人格障碍”的跨学科思考。
- 批准号:
ES/L000911/2 - 财政年份:2017
- 资助金额:
$ 53.24万 - 项目类别:
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ANAMMARKS: ANaerobic AMmonium oxidiation bioMARKers in paleoenvironmentS
ANAMMARKS:古环境中的厌氧铵氧化生物标志物
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NE/N011112/1 - 财政年份:2016
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$ 53.24万 - 项目类别:
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Newcastle University Confidence in Concept 2014
纽卡斯尔大学 2014 年理念信心
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MC_PC_14101 - 财政年份:2015
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$ 53.24万 - 项目类别:
Intramural
Large area two dimensional mapping of carbon dioxide fluxes for assessment and control of carbon capture and storage project
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- 批准号:
ST/L00626X/1 - 财政年份:2014
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$ 53.24万 - 项目类别:
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