computational identification and modeling of crosstalk between phosphorylation, o-β-glycosylation and methylation of foxo3 and implications for cancer therapeutics计算识别和建模磷酸化之间的串扰,o-β-glycosylation foxo3的甲基化和对癌症治疗的影响.pdfVIP
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computational identification and modeling of crosstalk between phosphorylation, o-β-glycosylation and methylation of foxo3 and implications for cancer therapeutics计算识别和建模磷酸化之间的串扰,o-β-glycosylation foxo3的甲基化和对癌症治疗的影响
Int. J. Mol. Sci. 2012, 13, 2918-2938; doi:10.3390/ijm OPEN ACCESS International Journal of Molecular Sciences ISSN 1422-0067 /journal/ijms Article Computational Identification and Modeling of Crosstalk between Phosphorylation, O-β-glycosylation and Methylation of FoxO3 and Implications for Cancer Therapeutics Azeem Mehmood Butt 1,2,†, Dandan Feng 2,†, Muhammad Idrees 1, Yigang Tong 3 and Jun Lu 2,* 1 Division of Molecular Virology, National Centre of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore 53700, Pakistan; E-Mails: azeem@.pk (A.M.B.); idreeskhan@.pk (M.I.) 2 Cancer Biotherapy Ward, Beijing YouAn Hospital, Capital Medical University, FengTai District, Beijing 100069, China; E-Mail: fengdandan83@ 3 State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China; E-Mail: tong62035@ † These authors contributed equally to this work. * Author to whom correspondence should be addressed; E-Mail: lujun98@; Tel./Fax: +86-10-6329-1028. Received: 30 January 2012; in revised form: 23 February 2012 / Accepted: 28 February 2012 / Published: 5 March 2012 Abstract: FoxO3 is a member of the forkhead class of transcription factors and plays a major role in the regulation of diverse cellular processes, including cell cycle arrest, DNA repair, and protection from stress stimuli by detoxification of reactive oxygen species. In addition, FoxO3 is a
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