期刊文献+

Prediction of functional phosphorylation sites by incorporating evolutionary information

原文传递
导出
摘要 Protein phosphorylation is a ubiquitous protein post-translational modification,which plays an important role in cellular signaling systems underlying various physiological and pathological processes.Current in silico methods mainly focused on the prediction of phosphorylation sites,but rare methods considered whether a phosphorylation site is functional or not.Since functional phosphorylation sites are more valuable for further experimental research and a proportion of phosphorylation sites have no direct functional effects,the prediction of functional phosphorylation sites is quite necessary for this research area.Previous studies have shown that functional phosphorylation sites are more conserved than non-functional phosphorylation sites in evolution.Thus,in our method,we developed a web server by integrating existing phosphorylation site prediction methods,as well as both absolute and relative evolutionary conservation scores to predict the most likely functional phosphorylation sites.Using our method,we predicted the most likely functional sites of the human,rat and mouse proteomes and built a database for the predicted sites.By the analysis of overall prediction results,we demonstrated that protein phosphorylation plays an important role in all the enriched KEGG pathways.By the analysis of protein-specific prediction results,we demonstrated the usefulness of our method for individual protein studies.Our method would help to characterize the most likely functional phosphorylation sites for further studies in this research area.
出处 《Protein & Cell》 SCIE CSCD 2012年第9期675-690,共16页 蛋白质与细胞(英文版)
基金 supported by the National Basic Research Program(973 Program)(Nos.2011CB910204,2010CB529206 and 2010CB912702) Research Program of Chinese Academy of Sciences(Nos.KSCX2-EW-R-04,KSCX2-YW-R-190 and 2011KIP204) National Natural Science Foundation of China(Grant Nos.30900272 and 31070752) Chinese Ministry for Science and Technology Grant(No.2008BAI64B01) the National High Technology Research and Development Program(863 Program)(No.2009AA02Z304).
  • 相关文献

参考文献2

二级参考文献34

  • 1LI Manyu,FAN Hengyu,TONG Chao,CHEN Dayuan,XIA Guoliang,SUN Qingyuan.MAPK regulates cell cycle progression in pig oocytes and fertilized eggs[J].Chinese Science Bulletin,2002,47(10):843-847. 被引量:1
  • 2Brauer KM, Werth D, von Schwarzenberg K, Bringmann A, Kanz L, Grunebach F, et al. BCR-ABL activity is critical for the immunogenicity of chronic myelogenous leukemia cells. Cancer Res 2007; 67: 5489-97.
  • 3Goldman JM, Melo N. Chronic myeloid leukemia - advances in biology and new approaches to treatment. N Engl J Med 2003; 349: 1451-64.
  • 4Goldman JM, Melo N. Targeting the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med 2001; 344: 1084-6.
  • 5Yoshida C, Yoshida F, Sears DE, Hart SM, Ikebe D, Muto A, et al. BcrAbl signaling through the PI-3jS6 kinase pathway inhibits nuclear translocation of the transcription factor Bach2, which represses the antiapoptotic factor heme oxygenase-l. Blood 2007; 109: 1211-9.
  • 6Strout MP, Schatz DG. Imatinib resistance and progression of CML to blast crisis: somatic hypermutation AIDing the way. Cancer Cell 2009; 16: 174-6.
  • 7lu Z, Jin Y, Chen C, Li J, Cao Q, Pan J. Pristimerin induces apoptosis in imatinib-resistant chronic myelogenous leukemia cells harboring T3151 mutation by blocking NF-kappaB signaling and depleting BcrAbl. Mol Cancer 2010; 9: 112.
  • 8Deguchi Y, Kimura S, Ashihara E, Niwa T, Hodohara K, Fujiyama Y, et al. Comparison of imatinib, dasatinib, nilotinib and INNO-406 in imatinib-resistant cell lines. Leuk Res 2008; 32: 980-3.
  • 9Rogakou EP, Pilch DR, Orr AH, Ivanova VS, Bonner WM. DNA doublestranded breaks induce histone H2AX phosphorylation on serine 139. J Biol Chem 1998; 273: 5858-68.
  • 10Lu C, Zhu F, Cho YY, Tang F, Zykova T, Ma WY, et al. Cell apoptosis: requirement of H2AX in DNA ladder formation, but not for the activation of caspase-3. Mol Cell 2006; 23: 121-32.

共引文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部