New Computational Methods for Data-driven Protein Structure Prediction
New Computational Methods for Data-driven Protein Structure Prediction
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
关键词:
AbbreviationsAddressAlgorithmsAmino Acid SequenceBiologicalBiological ProcessCell CommunicationCellsClassificationComplexComputing MethodologiesCouplingCrystallographyDataDevelopmentDiseaseFamily SizesFoundationsGenetic TranscriptionGeometryGoalsHealth Care CostsHomology ModelingHydrogen BondingKnowledgeLearningLifeMachine LearningMaintenanceMembrane ProteinsMetabolismMethodsModelingMolecular BiologyMolecular ConformationOccupationsPharmaceutical PreparationsPlayPreventive therapyProcessProtein FamilyProteinsResidual stateResourcesRoleSequence HomologsStructureStructure-Activity RelationshipSystemTimeTorsionTrainingTranslationsVariantVertebral columnWorkbiological researchcomputerized toolsconvolutional neural networkdeep learningdeep learning algorithmexperimental studyhuman diseaseimprovedlearning strategymodel buildingneural networknovel diagnosticsnovel therapeuticsprediction algorithmpredictive modelingprotein foldingprotein functionprotein structureprotein structure predictionsimulationsupervised learningtherapeutic developmentthree-dimensional modelingweb server
中文摘要
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.
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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
DOI:
10.1142/9789814583220_0015
发表时间:
2013-11
期刊:
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
影响因子:
--
作者:
[Fan Yang;Jinbo Xu;Jianyang Zeng]
通讯作者:
Fan Yang;Jinbo Xu;Jianyang Zeng
共 40 条
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:8269822
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项目类别:
-
资助金额:$26.59万
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财政年份:2010
-
负责人:JINBO XU
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依托单位:
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:8657055
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项目类别:
-
资助金额:$26.59万
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财政年份:2010
-
负责人:JINBO XU
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依托单位:
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:7764110
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项目类别:
-
资助金额:$26.86万
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财政年份:2010
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负责人:JINBO XU
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依托单位:
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:10477350
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项目类别:
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资助金额:$32.4万
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财政年份:2010
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负责人:JINBO XU
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依托单位:
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:8463561
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项目类别:
-
资助金额:$25.66万
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财政年份:2010
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负责人:JINBO XU
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依托单位:
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:8072026
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项目类别:
-
资助金额:$26.59万
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财政年份:2010
-
负责人:JINBO XU
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依托单位:
New Computational Methods for Data-driven Protein Structure Prediction
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批准号:10246779
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项目类别:
-
资助金额:$32.16万
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财政年份:2010
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负责人:JINBO XU
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依托单位:
A STUDY OF THE INTEROPERABILITY BETWEEN TERAGRID AND CNGRID BY EXPERIMENTING RE
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批准号:7723215
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项目类别:
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资助金额:$0.05万
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财政年份:2008
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负责人:JINBO XU
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依托单位:
A STUDY OF THE INTEROPERABILITY BETWEEN TERAGRID AND CNGRID BY EXPERIMENTING RE
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批准号:7601478
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项目类别:
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资助金额:$0.03万
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财政年份:2007
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负责人:JINBO XU
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依托单位:
海外基金