Structural Biology of sulfotransferase and glycosyltransferase
Structural Biology of sulfotransferase and glycosyltransferase
批准号:
7593958
负责人:
MASAHIKO NEGISHI
金额:
$38.81万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AffectAffinityAromataseBindingBinding ProteinsBiologicalBiological ProcessBlood coagulationCancer PatientChondroitinChondroitin SulfatesClinicalCommunicationCrystallographyDiseaseDrug Metabolic DetoxicationEnzymesEstrogensGenesGoalsGolgi ApparatusHIVHomeostasisInfectionInorganic SulfatesMembraneMethodsMolecularPharmaceutical PreparationsPlayPolysaccharidesProtein-Carbohydrate InteractionProteinsReactionRecombinant ProteinsResearchRoentgen RaysRoleSignaling MoleculeSiteSolutionsSpecificityStructureSulfatasesSystemTitrationsUnspecified or Sulfate Ion Sulfatesbasecell growthfrontierglycosyltransferasemalignant breast neoplasmmicrobialoutcome forecaststeroid hormonestructural biologysugarsulfotransferasesynthetic enzymethree dimensional structure
中文摘要
细胞溶质ST硫酸化异种化学物质用于解毒和分泌,并且还硫酸化生物信号分子如类固醇激素和生物胺用于灭活和/或储存。某些硫酸盐产品会致癌。高尔基体膜ST对多糖的硫酸化位点具有高度特异性。各种糖基转移酶合成多糖并为ST提供底物。我们的研究目标是阐明这些酶的结构和功能。为此,我们利用细菌表达系统生产了大量的重组蛋白,并将其结晶,并解决了它们的三维结构。等温滴定量热法也可用于研究溶液中各种分子间的相互作用。
英文摘要
Cytosolic STs sulfate xenochemicals for detoxification and secretion and also sulfate biological signal molecules such as steroid hormones and bioamines for inactivation and/or storage. Certain sulfated products become carcinogenic. Golgi-membrane STs display high specificity to sulfate distinct sites of polysaccharides. Various glycosyltransferases synthesize polysaccharides and provide STs with substrates. Our research objectives are to eluciadte structure and function of these enzymes. For this, we have used bacterial expression system to produce a large amount of recombinant proteins, have crystallized them, and have solved their 3-dimensional structures. Also Isothermal titration carlimetry is used to investigate various molecular interactactions in solution.
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Two-step mechanism that determines the donor binding specificity of human UDP-N-acetylhexosaminyltransferase.
确定人 UDP-N-乙酰己糖胺转移酶供体结合特异性的两步机制。
DOI:
10.1074/jbc.m413379200
发表时间:
2005
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Sobhany,Mack, Dong,Jian, Negishi,Masahiko]
通讯作者:
Negishi,Masahiko
Phenobarbital and Insulin Reciprocate Activation of the Nuclear Receptor Constitutive Androstane Receptor through the Insulin Receptor.
苯巴比妥和胰岛素通过胰岛素受体相互激活核受体组成型雄甾烷受体。
DOI:
10.1124/jpet.116.232140
发表时间:
2016
期刊:
The Journal of pharmacology and experimental therapeutics
影响因子:
--
作者:
[Yasujima,Tomoya, Saito,Kosuke, Moore,Rick, Negishi,Masahiko]
通讯作者:
Negishi,Masahiko
DOI:
10.1038/srep14076
发表时间:
2015-09-22
期刊:
Scientific reports
影响因子:
4.6
作者:
[Gotoh S, Negishi M]
通讯作者:
Negishi M
DOI:
10.1021/jm010171u
发表时间:
2001-07
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Dawn E. Verdugo;M. Cancilla;Xue Ge;Nathanael S. Gray;Young-Tae Chang;Peter G. Schultz;Masahiko Negishi-Masahi]
通讯作者:
Dawn E. Verdugo;M. Cancilla;Xue Ge;Nathanael S. Gray;Young-Tae Chang;Peter G. Schultz;Masahiko Negishi-Masahi
A phosphorylation-deficient mutant of retinoid X receptor α at Thr 167 alters fasting response and energy metabolism in mice.
类维生素A X 受体α 在Thr 167 处的磷酸化缺陷突变体改变了小鼠的禁食反应和能量代谢。
DOI:
10.1038/s41374-019-0266-1
发表时间:
2019
期刊:
Laboratory investigation; a journal of technical methods and pathology
影响因子:
--
作者:
[Sueyoshi,Tatsuya, Sakuma,Tsutomu, Shindo,Sawako, Fashe,Muluneh, Kanayama,Tomohiko, Ray,Manas, Moore,Rick, Negishi,Masahiko]
通讯作者:
Negishi,Masahiko
共 6 条
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:8336594
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项目类别:
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资助金额:$334.72万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:10004464
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项目类别:
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资助金额:$262.09万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:9352118
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项目类别:
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资助金额:$235.45万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanism and biological consequences of the nuclear rec
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批准号:7169993
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Pharmacogenetics Of Microsomal Steroid Hydroxylases
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批准号:6508872
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项目类别:
-
资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:8929756
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项目类别:
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资助金额:$269.66万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Structural Study of Sulfotransferases
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批准号:6227948
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Structural Biology of sulfotransferase and glycosyltrans
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批准号:7328841
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:8149056
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项目类别:
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资助金额:$384.44万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:8734114
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项目类别:
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资助金额:$235.22万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Activation Mechanism of the nuclear receptor CAR
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批准号:7007473
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Structural Biology of sulfotransferase and glycosyltrans
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批准号:6838567
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项目类别:
-
资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
DEVELOPMENTAL PHARMACOGENETICS OF MICROSOMAL STEROID HYDROXYLASES
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批准号:6432408
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项目类别:
-
资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
DEVELOPMENTAL PHARMACOGENETICS OF MICROSOMAL STEROID HYDROXYLASES
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批准号:6290069
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Structural Study Of Sulfotransferases
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批准号:6508870
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanisms and biological consequences of the nuclear receptor CAR activation
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批准号:10253780
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项目类别:
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资助金额:$259.87万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Structural Study of Sulfotransferases
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批准号:6432404
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Developmental Pharmacogenetics Of Microsomal Steroid Hyd
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批准号:6681992
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Mechanism and biological consequences of the nuclear rec
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批准号:7328859
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
Structural Biology of sulfotransferase and glycosyltrans
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批准号:7007467
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:MASAHIKO NEGISHI
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依托单位:
海外基金