NMR chemical shift assignments of a complex between SUMO-1 and SIM peptide derived from the C-terminus of Daxx

Mandar T. Naik, Che Chang Chang, Nandita M. Naik, Camy C.H. Kung, Hsiu Ming Shih, Tai Huang Huang*

*此作品的通信作者

研究成果: 雜誌貢獻期刊論文同行評審

3 引文 斯高帕斯(Scopus)

摘要

Small Ubiquitin-like MOdifiers (SUMOs) are ubiquitin-like proteins known to covalently modify large number of cellular proteins. The mammalian SUMO family includes four paralogues, SUMO-1 through SUMO-4. Death-associated protein-6, Daxx, is a 740 residue important transcription corepressor known to represses transcriptional potential of several sumolyted transcription factors. Daxx also plays important role in apoptosis. Both terminals of Daxx harbor separate SUMO Interaction Motifs (SIM), which mediate its interaction with SUMO and hence the sumolyted transcription factors. The C-terminal SIM of Daxx preferentially binds SUMO-1. Practically complete 1H, 13C and 15N resonance assignments for the complex between SUMO-1 and 20 residue Daxx C-terminal SIM peptide are reported here.

原文英語
頁(從 - 到)75-77
頁數3
期刊Biomolecular NMR Assignments
5
發行號1
DOIs
出版狀態已發佈 - 2011 4月
對外發佈

ASJC Scopus subject areas

  • 結構生物學
  • 生物化學

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