教授
性别：男
在职信息：在职
所在单位：基础医学院
入职时间：2012-07-16
访问量：
最后更新时间：..
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[21]
刘琪.
DeSiphering receptor core-induced and ligand-dependent conformational changes in arrestin via genetic encoded trimethylsilyl H-1-NMR probe.
Nature Communications,
11,
2020.
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[22]
卢志远.
Identification of HN252 as a potent inhibitor of protein phosphatase PPM1B.
journal of cellular and molecular medicine,
24,
13463,
2020.
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[23]
黄申明.
Structural basis of signaling of cannabinoids receptors: paving a way for rational drug design in controling mutiple neurological and immune diseases.
SIGNAL TRANSDUCTION AND TARGETED THERAPY,
2020.
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[24]
黄深明.
Structural basis of signaling of cannabinoids receptors: paving a way for rational drug design in controling mutiple neurological and immune diseases.
SIGNAL TRANSDUCTION AND TARGETED THERAPY,
5,
2020.
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[25]
杨帆.
Structural basis of GPBAR activation and bile acid recognition.
Nature,
587,
499,
2020.
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[26]
杨帆.
Structural basis of GPBAR activation and bile acid recognition.
Nature,
2020.
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[27]
梁啸.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one derivatives as lymphoid-specific tyrosine phosphatase inhibitors.
BIOORGANIC CHEMISTRY,
103,
2020.
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[28]
方浩 and 侯旭奔.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one derivatives as lymphoid-specific tyrosine phosphatase inhibitors.
Bioorg Chem.,
2020.
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[29]
Dolatabad, Meisam Rostaminasab.
Crystal structure and catalytic activity of the PPM1K N94K mutant.
Journal of Neurochemistry,
148,
550,
2019.
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[30]
李康帅.
Identification and structure-function analyses of an allosteric inhibitor of the tyrosine phosphatase PTPN22.
294,
8653,
2019.
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[31]
肖鹏 , 孙金鹏 and 龚秋雨.
Internal standard fluorogenic probe based on vibration-induced emission for visualizing PTP1B in living cells..
Chemical communications,
56,
58,
2019.
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[32]
张鹏举 , 孙金鹏 , 肖鹏 , 沈月毛 , 于晓 and ROSTAMINASAB DOLATABAD MEISAM.
Crystal structure and catalytic activity of the PPM1K N94K mutant..
Journal of Neurochemistry,
148,
550,
2019.
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[33]
于晓 , 方浩 , 孙金鹏 , 肖鹏 and 李康帅.
Identification of para-Substituted Benzoic Acid Derivatives as Potent Inhibitors of the Protein Phosphatase Slingshot.
CHEMMEDCHEM,
10,
1980,
2015.
-
[34]
肖鹏 , 崔福爱 , 于晓 , 毕文祥 and 孙金鹏.
The second-sphere residue T263 is important for the function and catalytic activity of PTP1B via interaction with the WPD-loop.
The International Journal of Biochemistry& Cell Biology,
57,
84,
2014.
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[35]
杨照 , 肖鹏 , 于晓 and 孙金鹏.
G蛋白偶联受体的信号通路多样性及药物开发.
中国科学:生命科学,
2018.
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[36]
于晓 , 孙金鹏 , 方浩 , 沈月毛 , 徐志刚 , 肖鹏 , 何东方 , 杨笃晓
Allosteric modulation of the catalytic VYD loop in Slingshot by its N-terminal domain underlies both Slingshot auto-inhibition and activation.
Journal of biological chemistry,
293,
16226,
2018.
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[37]
易凡 , 于晓 , 沈月毛 , 孙金鹏 , 何东方 , 肖鹏 and 杨帆.
Allosteric mechanisms underlie GPCR signaling to SH3-domain proteins through arrestin.
NATURE CHEMICAL BIOLOGY,
14,
876,
2018.
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[38]
徐志刚 , 于晓 , 孙金鹏 , 张鹏举 , 肖鹏 , 李慧
Switching of the substrate specificity of protein tyrosine phosphatase N12 by cyclin-dependent kinase 2 phosphorylation orchestrating 2 oncogenic pathways.
FASEB Journal,
32,
73,
2018.
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[39]
孙金鹏 , 肖鹏 and 张华堂.
Construction of an alkaline phosphatase-specific two-photon probe and its imaging application in living cells and tissues.
Biomaterials,
140,
220,
2017.
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[40]
杨照 , 孙金鹏 , 杨帆 , 肖鹏 and 于晓.
Phosphorylation of G Protein-Coupled Receptors: From the Barcode Hypothesis to the Flute Model.
Molecular Pharmacology,
92,
201,
2017.
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