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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[41]
刘春华 , 刘传勇 , 易凡 , 于晓 , 孙金鹏 , 肖鹏 , 崔福爱 and 何东方.
Arrestin-biased AT1R agonism induces acute catecholamine secretion through TRPC3 coupling.
NATURE COMMUNICATIONS,
8,
2017.
-
[42]
孙金鹏 , 于晓 , 肖鹏 , 任桂杰 and 方浩.
Identification of a benzo imidazole thiazole derivative as the specific irreversible inhibitor of protein tyrosine phosphatase..
Bioorg Med Chem Lett.,
2016 Oct 1;26(19):4795-8.,
4795,
2016.
-
[43]
于晓 , 肖鹏 , 崔福爱 , 易凡 , 徐志刚 and 孙金鹏.
Crystal Structure and Substrate Specificity of PTPN12..
Cell Reports.,
15,
1345,
2016.
-
[44]
孙金鹏 , 肖鹏 and 于晓.
The catalytic role of the M2 metal ion in PP2Cα..
scientific reports,
5,
8560,
2015.
-
[45]
肖鹏 and 孙金鹏.
Discovery of GPCR superfamily and elucidation its working mechanisms and structures, to decode 2012 Nobel Prize in Chemistry.
Progress in Biochemistry and Biophysics,
39,
1050,
2012.
-
[46]
侯旭奔 , 孙金鹏 , 方浩 and 肖鹏.
Computational Strategy for Bound State Structure Prediction in Structure-Based Virtual Screening: A Case Study of Protein Tyrosine Phosphatase Receptor Type O Inhibitors.
Journal of Chemical Information and Modeling,
58,
2331,
2018.
-
[47]
何东方 and 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.
-
[48]
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.
-
[49]
于晓 , 肖鹏 , 方浩 and 孙金鹏.
Identification of a benzo imidazole thiazole derivative as the specific irreversible inhibitor of protein tyrosine phosphatase..
Bioorg Med Chem Lett.,
2016 Oct 1;26(19):4795-8.,
4795,
2016.
-
[50]
肖鹏 , 孙金鹏 and 于晓.
Crystal Structure and Substrate Specificity of PTPN12..
Cell Reports.,
15,
1345,
2016.
-
[51]
肖鹏 , 于晓 and 孙金鹏.
The catalytic role of the M2 metal ion in PP2Cα..
scientific reports,
5,
8560,
2015.
-
[52]
沈月毛 , 于晓 , 张鹏举 , 肖鹏 and 孙金鹏.
Crystal structure and catalytic activity of the PPM1K N94K mutant..
Journal of Neurochemistry,
148,
550,
2019.
-
[53]
孙金鹏 , 方浩 , 肖鹏 and 侯旭奔.
Computational Strategy for Bound State Structure Prediction in Structure-Based Virtual Screening: A Case Study of Protein Tyrosine Phosphatase Receptor Type O Inhibitors.
Journal of Chemical Information and Modeling,
58,
2331,
2018.
-
[54]
杨帆 , 肖鹏 , 于晓 , 孙金鹏 and 杨照.
Phosphorylation of G Protein-Coupled Receptors: From the Barcode Hypothesis to the Flute Model.
Molecular Pharmacology,
92,
201,
2017.
-
[55]
崔福爱 , 徐志刚 , 易凡 , 孙金鹏 , 肖鹏 and 于晓.
Crystal Structure and Substrate Specificity of PTPN12..
Cell Reports.,
15,
1345,
2016.
-
[56]
任桂杰 , 方浩 , 肖鹏 , 于晓 and 孙金鹏.
Identification of a benzo imidazole thiazole derivative as the specific irreversible inhibitor of protein tyrosine phosphatase..
Bioorg Med Chem Lett.,
2016 Oct 1;26(19):4795-8.,
4795,
2016.
-
[57]
于晓 , 肖鹏 and 孙金鹏.
The catalytic role of the M2 metal ion in PP2Cα..
scientific reports,
5,
8560,
2015.
-
[58]
何东方 , 易凡 , 沈月毛 , 于晓 , 孙金鹏 , 肖鹏 and 杨帆.
Allosteric mechanisms underlie GPCR signaling to SH3-domain proteins through arrestin.
NATURE CHEMICAL BIOLOGY,
14,
876,
2018.
-
[59]
何东方 and 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.
-
[60]
肖鹏 , 于晓 , 孙金鹏 and 杨照.
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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