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New Computational Methods for Data-driven Protein Structure Prediction

New Computational Methods for Data-driven Protein Structure Prediction
数据驱动的蛋白质结构预测的新计算方法
批准号:
10693195
负责人:
JINBO XU
金额:
$32.66万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-05-14 至 2024-08-31

项目摘要

项目成果

JINBO XU的其他基金

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相关文献

中文摘要
翻译
蛋白质在所有的生物过程中起着基本的作用。准确描述蛋白质
英文摘要
Proteins play fundamental roles in all biological processes. Accurate description of protein structure is an important step towards understanding of biological life and highly relevant in the development of therapeutics and drugs. Although experimental structure determination has been greatly improved, there is still a very large gap between the number of available protein sequences and that of solved protein structures, which can only be filled by computational prediction. The long-term goal of this project is to apply machine learning and optimization algorithms to understand protein sequence-structure-function relationship by analyzing sequence, structure and functional data and to develop data-driven computational methods and tools for structure and functional prediction. We believe that by developing sophisticated algorithms to extract knowledge from the increasing sequence and structure data, we can model protein sequence-structure relationship very accurately and improve structure and functional prediction greatly. This project has already produced a few CASP-winning, widely-used data- driven algorithms and web servers (http://raptorx.uchicago.edu) for protein structure modeling. This renewal will further develop machine learning (especially deep learning) algorithms for protein structure modeling without good templates. The specific aims are: (1) developing deep learning (DL) algorithms for the prediction of protein contact and distance matrix; (2) developing distance-based algorithms for fast and accurate ab initio folding of proteins without templates; (3) developing DL algorithms for template-based modeling with only weakly similar templates. This renewal will lead to further understanding and new models of protein sequence-structure relationship and yield publicly available resources for automated, accurate, quantitative analysis for a wide range of proteins. The impact will be multiplied by tens of thousands of worldwide users employing our web servers to study a wide variety of proteins relevant to basic biological research and human diseases, in both low- and high-throughput experiments.
期刊论文(59)
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科研奖励(0)
会议论文
DOI: 10.1093/nar/gky420
发表时间: 2018-07-02
期刊: Nucleic acids research
影响因子: 14.9
作者: [Zeng H, Wang S, Zhou T, Zhao F, Li X, Wu Q, Xu J]
通讯作者: Xu J
Inferential modeling of 3D chromatin structure.
3D 染色质结构的推理建模
DOI: 10.1093/nar/gkv100
发表时间: 2015-04-30
期刊: Nucleic acids research
影响因子: 14.9
作者: [Wang S, Xu J, Zeng J]
通讯作者: Zeng J
DOI: 10.1002/prot.23016
发表时间: 2011-06
期刊: PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
影响因子: 2.9
作者: [Peng, Jian, Xu, Jinbo]
通讯作者: Xu, Jinbo
DOI: 10.1038/s43588-021-00098-9
发表时间: 2021-07
期刊: Nature computational science
影响因子: --
作者: [Jing X, Xu J]
通讯作者: Xu J
共 40 条
    New Computational Methods for Data-driven Protein Structure Prediction
    New Computational Methods for Data-driven Protein Structure Prediction
    New Computational Methods for Data-driven Protein Structure Prediction
    New Computational Methods for Data-driven Protein Structure Prediction
    海外基金