NE-CAT: A Resource for Advanced Macromolecular Crystallography
NE-CAT: A Resource for Advanced Macromolecular Crystallography
批准号:
10505648
负责人:
Nozomi Ando
金额:
$379.29万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
未结题
起止时间:
2018-04-01 至 2028-03-31
关键词:
20 year oldAdvisory CommitteesAgingAreaAutomatic Data ProcessingBiologicalBiological ProcessBiomedical ResearchCharacteristicsCommunitiesComputer softwareCrystallographyData AnalysesData CollectionDedicationsDevelopmentEducation and OutreachEducational workshopEnsureFundingGoalsGroupingHealthcareIndividualInfrastructureInstitutionLogisticsMainstreamingMaintenanceManuscriptsModificationOpticsPaperPersonsPharmacologic SubstancePhotonsProductivityProfessional OrganizationsPublicationsPublishingRecruitment ActivityResearchResearch PersonnelResearch Project GrantsResourcesRoboticsRoentgen RaysRunningSamplingScheduleSiteSourceStructureSynchrotronsSystemTechniquesTechnologyTimeTrainingTraining ActivityTraining ProgramsUnited States National Institutes of HealthUniversitiesWorkbeamlinebiological systemscomputerized data processingdata structuredesigndetectorexperienceimprovedmacromoleculemeetingsmemberoperationoutreachoutreach programprogramsrepairedthree dimensional structurethree-dimensional visualizationweb based interfaceweb site
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The main goal of NE-CAT is to provide user access to state-of-the-art synchrotron beamlines for
macromolecular crystallography. NE-CAT began planning and design for two beamlines in 2001. Beamline
24-ID-C became available to Advanced Photon Source users in 2006 and beamline 24-ID-E became
available in 2007. During the ensuing years, beamline improvements have resulted in stable, small X-ray
beams ideally suited for challenging problems in macromolecular crystallography. Each beamline is
equipped with a high capacity sample automounter and a microdiffractometer. Beamline 24-ID-C features
an EIGER2 X 16M pixel array detector, and 24-ID-E features an EIGER X 16M. NE-CAT provides
automated software for data collection and analysis (RAPD) and a web-based interface for remote data
collection. We will continue to provide routine maintenance to ensure efficient and reliable data collection,
and we propose an upgrade program to maintain state-of-the-art capabilities over the five years covered by
this application. This period includes 12 months without X-rays required for the APS upgrade project. We
will use this superb opportunity to rebuild a nearly 20-year-old system to be leaders in the field for another
20 years. NE-CAT has an experienced and dedicated scientific staff who enable access to the beamlines.
The staff is available or on call 24/7 to assist users with data collection and processing needs. This highly
regarded staff is a major strength of NE-CAT. NE-CAT has an outstanding record of reliability with technical
problems rarely interfering with user access. NE-CAT is directed by Dr. Steven Ealick, who has more that
30 years of experience overseeing the operation of synchrotron facilities for macromolecular
crystallography. The technical group, led by Deputy Director Dr. Malcolm Capel, and the operations group,
led by Associate Director Dr. Frank Murphy work closely together to ensure that the needs of the user
community are met. Together, these three individuals make up the NE-CAT management team. NE-CAT
beam time is in high demand, and each run all available beam time is allocated to users. NE-CAT typically
hosts more than 1500 users per year from about 160 unique user groups, either on site or remotely. NE-
CAT users published about 200 papers during the last year and are projected to publish more than 190 in
2021. NE-CAT’s record of productivity places it among the top of worldwide facilities for macromolecular
crystallography. NE-CAT operates an extensive user training program adaptable to first time users,
advanced users with technically challenging problems, and everyone in between. A website is available to
provide all information needed by new or current users. NE-CAT participates in many training and outreach
activities including organization of an annual workshop and participation in professional society meetings.
The staff works closely with user groups and are often invited to coauthor manuscripts resulting from user
support and training.
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Correction to "A Fluorescence Polarization Assay for Macrodomains Facilitates the Identification of Potent Inhibitors of the SARS-CoV-2 Macrodomain".
对“宏结构域的荧光偏振测定有利于识别 SARS-CoV-2 宏结构域的有效抑制剂”的更正。
DOI:
10.1021/acschembio.4c00159
发表时间:
2024
期刊:
ACS chemical biology
影响因子:
4
作者:
[Anmangandla,Ananya, Jana,Sadhan, Peng,Kewen, Wallace,ShamarD, Bagde,SaketR, Drown,BryonS, Xu,Jiashu, Hergenrother,PaulJ, Fromme,JChristopher, Lin,Hening]
通讯作者:
Lin,Hening
Structural basis for Tpt1-catalyzed 2'-PO4 transfer from RNA and NADP(H) to NAD.
Tpt1 催化 2-PO4 从 RNA 和 NADP(H) 转移到 NAD 的结构基础。
DOI:
10.1073/pnas.2312999120
发表时间:
2023
期刊:
Proceedings of the National Academy of Sciences of the United States of America
影响因子:
11.1
作者:
[Jacewicz,Agata, Dantuluri,Swathi, Shuman,Stewart]
通讯作者:
Shuman,Stewart
Racemic Peptides from Amyloid β and Amylin Form Rippled β-Sheets Rather Than Pleated β-Sheets.
来自β淀粉样蛋白和胰淀素的外消旋肽形成波纹状β-片而不是褶状β-片。
DOI:
10.1021/jacs.3c11712
发表时间:
2023
期刊:
Journal of the American Chemical Society
影响因子:
15
作者:
[Hazari,Amaruka, Sawaya,MichaelR, Sajimon,Maria, Vlahakis,Niko, Rodriguez,Jose, Eisenberg,David, Raskatov,JevgenijA]
通讯作者:
Raskatov,JevgenijA
An ensemble of lipoxygenase structures reveals novel conformations of the Fe coordination sphere.
脂氧合酶结构的集合揭示了 Fe 配位球的新构象。
DOI:
10.1002/pro.3602
发表时间:
2019
期刊:
Protein science : a publication of the Protein Society
影响因子:
--
作者:
[Pakhomova,Svetlana, Boeglin,WilliamE, Neau,DavidB, Bartlett,SueG, Brash,AlanR, Newcomer,MarciaE]
通讯作者:
Newcomer,MarciaE
DOI:
10.3390/v13040663
发表时间:
2021-04-12
期刊:
Viruses
影响因子:
--
作者:
[Tang H, Demir Ö, Kurniawan F, Brown WL, Shi K, Moeller NH, Carpenter MA, Belica C, Orellana K, Du G, LeBeau AM, Amaro RE, Harris RS, Aihara H]
通讯作者:
Aihara H
共 179 条
Protein Allostery and Catalysis Beyond Bragg Diffraction
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批准号:10677766
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项目类别:
-
资助金额:$41.5万
-
财政年份:2017
-
负责人:Nozomi Ando
-
依托单位:
Protein Allostery and Catalysis Beyond Bragg Diffraction
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批准号:10406516
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项目类别:
-
资助金额:$41.56万
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财政年份:2017
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负责人:Nozomi Ando
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依托单位:
Protein Allostery and Catalysis Beyond Bragg Diffraction
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批准号:10806507
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项目类别:
-
资助金额:$1.31万
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财政年份:2017
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负责人:Nozomi Ando
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依托单位:
Protein Allostery and Catalysis Beyond Bragg Diffraction
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批准号:10250499
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项目类别:
-
资助金额:$38.66万
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财政年份:2017
-
负责人:Nozomi Ando
-
依托单位:
Protein Allostery and Catalysis Beyond Bragg Diffraction
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批准号:10798624
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项目类别:
-
资助金额:$5.89万
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财政年份:2017
-
负责人:Nozomi Ando
-
依托单位:
Structural Characterizations of Transient and Heterogeneous Protein Complexes
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批准号:8895472
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项目类别:
-
资助金额:$24.9万
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财政年份:2012
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负责人:Nozomi Ando
-
依托单位:
Structural Characterizations of Transient and Heterogeneous Protein Complexes
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批准号:8417652
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项目类别:
-
资助金额:$8.55万
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财政年份:2012
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负责人:Nozomi Ando
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依托单位:
Structural Characterizations of Transient and Heterogeneous Protein Complexes
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批准号:8225883
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项目类别:
-
资助金额:$9.0万
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财政年份:2012
-
负责人:Nozomi Ando
-
依托单位:
Structural Studies of Ribonucleotide Reductase Complexes
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批准号:8013604
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项目类别:
-
资助金额:$5.13万
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财政年份:2010
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负责人:Nozomi Ando
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依托单位:
Structural Studies of Ribonucleotide Reductase Complexes
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批准号:7806713
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项目类别:
-
资助金额:$4.76万
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财政年份:2010
-
负责人:Nozomi Ando
-
依托单位:
海外基金