Structural Genomics of Eukaryotic Domain Families
Structural Genomics of Eukaryotic Domain Families
批准号:
8692872
负责人:
GAETANO T MONTELIONE
金额:
$681.89万
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:
2010-09-01 至 2016-06-30
关键词:
Amino Acid SequenceAreaBase SequenceBindingBioinformaticsBiologicalBiological SciencesBiologyBiomedical ResearchCancer BiologyCellsCerealsChemicalsCollaborationsCommunitiesComplementComplexComputer softwareComputing MethodologiesConsensusCouplingCrystallizationDataDatabasesDepositionDevelopmental BiologyDiseaseDisulfidesEducationEducational workshopEngineeringEscherichia coliFamilyFundingGenomicsGerm CellsGoalsGrantHealthHomology ModelingHumanHybridsInformation DisseminationInsect ProteinsInstitutesLigandsLightLiteratureMalignant NeoplasmsMethodsMissionModelingMolecular ChaperonesNIH Program AnnouncementsNational Institute of General Medical SciencesNatureNuclearOntarioPeptide Sequence DeterminationPhasePrincipal InvestigatorProcessProductionProtein Structure InitiativeProteinsProteomeProtocols documentationPublicationsReagentRelaxationResearchResearch InfrastructureResearch Project GrantsResidual stateResourcesRoentgen RaysSamplingScientistSequence AnalysisSolubilitySourceStructureSynchrotronsSystemTechnologyTertiary Protein StructureTrainingUnited States National Institutes of HealthUniversitiesWheatX-Ray Crystallographybasebiological researchcomputerized data processingdesign and constructionexpression vectorimprovedinstrumentknowledge basemeetingsmethod developmentmonomernew technologynext generationnovelprogramsprotein complexprotein expressionprotein structurerepositorystructural biologystructural genomicssuccesstechnology developmentthree dimensional structuretoolweb site
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The Northeast Structural Genomics Consortium (NESG) is one of four Large-Scale Centers (LSCs) for structure production funded by the NIH NIGMS Protein Structure Initiative (PSI). The goals of the PSI LSCs are to (i) generate three-dimensional (3D) structures for large numbers of proteins selected using broad biological, genomic, and bioinformatics criteria, together with targets selected from specific biological theme projects, so as to provide significant structural coverage of a large number of protein sequences In nature, (ii) develop and disseminate novel and/or improved technologies for structural biology and bioinformatics, and (iii) make these structures, structure production data, and the associated reagents and technologies publicly available to the worldwide scientific community. In PSI:Biology, the next phase of the PSI program, the NESG will expand Its mission by carrying our collaborative structural genomics projects together with several PSI Consortia for High-Through-Put (HTP) Enabled Structural Biology Partnerships (Biology Partnerships) and associated Program Announcements (PARs). The primary goal of the NESG In PSI:Biology is to provide > 1,100 new 3D protein structures to the Protein Data Bank (PDB) over 5 years, together with extensive raw and processed data, protocols for sample production, structure/function annotations, and thousands of homology models derived from these structures. This will complement the ~ 900 structures deposited by NESG in PSI Phases 1 and 2. In particular, NESG will provide novel 3D structural information useful in modeling large numbers of eukaryotic and human proteins. Our efforts will span five classes of target types: (i) proteins nominated In collaborations to be established with PSI Biology Partnerships, (ii) domain families (referred to as BIG, MEGA, and META families) defined by the central PSI:Biology Target Selection Subcommittee to provide course-grained coverage of large protein domain families; (iii) proteins defined by the NESG Biomedical Theme of 'Networks of Proteins Associated with Human Cancer and Developmental Biology'; (iv) proteins nominated by the general biomedical research community, and (v) proteins selected for specific technology-development goals. Protein targets in the first two of these classes, representing ~ 80% of the overall NESG effort, will be selected in a coordinated process together with the other LSCs and Biology Partnerships so as to maximize biological impact and minimize redundant efforts. The many methods and technologies for structural genomics research developed in this project will provide the next- generation tools for traditional hypothesis-driven biological research, and will thus have powerful and broad impact on the infrastructure for biological science and engineering.
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DOI:
10.1007/s10969-014-9185-y
发表时间:
2014-12
期刊:
Journal of structural and functional genomics
影响因子:
--
作者:
[Pulavarti SV, Huang YJ, Pederson K, Acton TB, Xiao R, Everett JK, Prestegard JH, Montelione GT, Szyperski T]
通讯作者:
Szyperski T
DOI:
10.1038/nature11600
发表时间:
2012-11-08
期刊:
Nature
影响因子:
64.8
作者:
[]
通讯作者:
DOI:
10.1038/nature16509
发表时间:
2016-01-21
期刊:
NATURE
影响因子:
64.8
作者:
[Boel, Gregory, Letso, Reka, Neely, Helen, Price, W. Nicholson, Wong, Kam-Ho, Su, Min, Luff, Jon D., Valecha, Mayank, Everett, John K., Acton, Thomas B., Xiao, Rong, Montelione, Gaetano T., Aalberts, Daniel P., Hunt, John F.]
通讯作者:
Hunt, John F.
DOI:
10.1007/s10969-013-9164-8
发表时间:
2013-12
期刊:
Journal of structural and functional genomics
影响因子:
--
作者:
[Pulavarti, Surya V S R K, Eletsky, Alexander, Lee, Hsiau-Wei, Acton, Thomas B, Xiao, Rong, Everett, John K, Prestegard, James H, Montelione, Gaetano T, Szyperski, Thomas]
通讯作者:
Szyperski, Thomas
DOI:
10.1016/j.bbrc.2014.03.068
发表时间:
2014-04-25
期刊:
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
影响因子:
3.1
作者:
[Helander, Sara, Montecchio, Meri, Lemak, Alexander, Fares, Christophe, Almof, Jonas, Li, Yanjun, Yee, Adelinda, Arrowsmith, Cheryl H., Dhe-Paganon, Sirano, Sunnerhagen, Maria]
通讯作者:
Sunnerhagen, Maria
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