نتایج جستجو برای: sumo

تعداد نتایج: 3544  

Journal: :The Journal of biological chemistry 2011
Eric Escobar-Cabrera Mark Okon Desmond K W Lau Christopher F Dart Alexandre M J J Bonvin Lawrence P McIntosh

DAXX is a scaffold protein with diverse roles that often depend upon binding SUMO via its N- and/or C-terminal SUMO-interacting motifs (SIM-N and SIM-C). Using NMR spectroscopy, we characterized the in vitro binding properties of peptide models of SIM-N and SIM-C to SUMO-1 and SUMO-2. In each case, binding was mediated by hydrophobic and electrostatic interactions and weakened with increasing i...

Journal: :Genes & development 2010
Yang Xie Eric M Rubenstein Tanja Matt Mark Hochstrasser

Many proteins are regulated by ubiquitin-dependent proteolysis. Substrate ubiquitylation can be stimulated by additional post-translational modifications, including small ubiquitin-like modifier (SUMO) conjugation. The recently discovered SUMO-targeted ubiquitin ligases (STUbLs) mediate the latter effect; however, no endogenous substrates of STUbLs that are degraded under normal conditions are ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Mark D Benson Qiu-Ju Li Katherine Kieckhafer David Dudek Matthew R Whorton Roger K Sunahara Jorge A Iñiguez-Lluhí Jeffrey R Martens

The voltage-gated potassium (Kv) channel Kv1.5 mediates the I(Kur) repolarizing current in human atrial myocytes and regulates vascular tone in multiple peripheral vascular beds. Understanding the complex regulation of Kv1.5 function is of substantial interest because it represents a promising pharmacological target for the treatment of atrial fibrillation and hypoxic pulmonary hypertension. He...

2017
Magdalena J. Mazur Benjamin J. Spears André Djajasaputra Michelle van der Gragt Georgios Vlachakis Bas Beerens Walter Gassmann Harrold A. van den Burg

In Arabidopsis more than 400 proteins have been identified as SUMO targets, both in vivo and in vitro. Among others, transcription factors (TFs) are common targets for SUMO conjugation. Here we aimed to exhaustively screen for TFs that interact with the SUMO machinery using an arrayed yeast two-hybrid library containing more than 1,100 TFs. We identified 76 interactors that foremost interact wi...

Journal: :Molecular cell 2009
Taras Makhnevych Yaroslav Sydorskyy Xiaofeng Xin Tharan Srikumar Franco J Vizeacoumar Stanley M Jeram Zhijian Li Sondra Bahr Brenda J Andrews Charles Boone Brian Raught

Systematic functional genomics approaches were used to map a network centered on the small ubiquitin-related modifier (SUMO) system. Over 250 physical interactions were identified using the SUMO protein as bait in affinity purification-mass spectrometry and yeast two-hybrid screens. More than 500 genes and 1400 synthetic genetic interactions were mapped by synthetic genetic array (SGA) analysis...

2013
Roland Steinacher Fekret Osman Alexander Lorenz Claire Bryer Matthew C. Whitby

The SUMO-dependent ubiquitin ligase Slx8 plays key roles in promoting genome stability, including the processing of trapped Topoisomerase I (Top1) cleavage complexes and removal of toxic SUMO conjugates. We show that it is the latter function that constitutes Slx8's primary role in fission yeast. The SUMO conjugates in question are formed by the SUMO ligase Pli1, which is necessary for limiting...

2015
Ivo A. Hendriks Rochelle C. D'Souza Jer-Gung Chang Matthias Mann Alfred C. O. Vertegaal

SUMOylation is a reversible post-translational modification (PTM) regulating all nuclear processes. Identification of SUMOylation sites by mass spectrometry (MS) has been hampered by bulky tryptic fragments, which thus far necessitated the use of mutated SUMO. Here we present a SUMO-specific protease-based methodology which circumvents this problem, dubbed Protease-Reliant Identification of SUM...

2012
Matthew Smith Wiam Turki-Judeh Albert J. Courey

Small ubiquitin-related modifier (SUMO), an ~90 amino acid ubiquitin-like protein, is highly conserved throughout the eukaryotic domain. Like ubiquitin, SUMO is covalently attached to lysine side chains in a large number of target proteins. In contrast to ubiquitin, SUMO does not have a direct role in targeting proteins for proteasomal degradation. However, like ubiquitin, SUMO does modulate pr...

2007
F. Z. Watts A. Skilton J. C. - Y. Ho L. K. Boyd M. A. M. Trickey L. Gardner F. - X. Ogi E. A. Outwin

SUMOylation is a post-translational modification that affects a large number of proteins, many of which are nuclear. While the role of SUMOylation is beginning to be elucidated, it is clear that understanding the mechanisms that regulate the process is likely to be important. Control of the levels of SUMOylation is brought about through a balance of conjugating and deconjugating activities, i.e...

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