نتایج جستجو برای: ubiquitin

تعداد نتایج: 28509  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
K G Murti H T Smith V A Fried

Immunofluorescence microscopy was used to study the intracellular localization of ubiquitin. Baby hamster kidney cells (BHK cells) and several other cell lines were probed with a well characterized monoclonal antibody to ubiquitin. The antibody stained a complex cellular structure that we identified as the microtubule network. The anti-ubiquitin antibody bound to the microtubule network at all ...

Journal: :Molecular cell 2016
Maximilian von Delbrück Andreas Kniss Vladimir V Rogov Lukas Pluska Katrin Bagola Frank Löhr Peter Güntert Thomas Sommer Volker Dötsch

Ubiquitin conjugation is an essential process modulating protein function in eukaryotic cells. Surprisingly, little is known about how the progressive assembly of ubiquitin chains is managed by the responsible enzymes. Only recently has ubiquitin binding activity emerged as an important factor in chain formation. The Ubc7 activator Cue1 carries a ubiquitin binding CUE domain that substantially ...

2012
Judith J Smit Davide Monteferrario Sylvie M Noordermeer Willem J van Dijk Bert A van der Reijden Titia K Sixma

Activation of the NF-κB pathway requires the formation of Met1-linked 'linear' ubiquitin chains on NEMO, which is catalysed by the Linear Ubiquitin Chain Assembly Complex (LUBAC) E3 consisting of HOIP, HOIL-1L and Sharpin. Here, we show that both LUBAC catalytic activity and LUBAC specificity for linear ubiquitin chain formation are embedded within the RING-IBR-RING (RBR) ubiquitin ligase subun...

Journal: :Journal of molecular biology 1999
K D Wilkinson E Laleli-Sahin J Urbauer C N Larsen G H Shih A L Haas S T Walsh A J Wand

The ubiquitin fold is a versatile and widely used targeting signal that is added post-translationally to a variety of proteins. Covalent attachment of one or more ubiquitin domains results in localization of the target protein to the proteasome, the nucleus, the cytoskeleton or the endocytotic machinery. Recognition of the ubiquitin domain by a variety of enzymes and receptors is vital to the t...

2015
Aya Toma Tomio S. Takahashi Yusuke Sato Atsushi Yamagata Sakurako Goto-Ito Shinichiro Nakada Atsuhiko Fukuto Yasunori Horikoshi Satoshi Tashiro Shuya Fukai

Several ubiquitin-binding zinc fingers (UBZs) have been reported to preferentially bind K63-linked ubiquitin chains. In particular, the UBZ domain of FAAP20 (FAAP20-UBZ), a member of the Fanconi anemia core complex, seems to recognize K63-linked ubiquitin chains, in order to recruit the complex to DNA interstrand crosslinks and mediate DNA repair. By contrast, it is reported that the attachment...

2017
Shisako Shoji Kazuharu Hanada Noboru Ohsawa Mikako Shirouzu

Really interesting new gene (RING)-finger protein 52 (RNF52), an E3 ubiquitin ligase, is found in eukaryotes from yeast to humans. Human RNF52 is known as breast cancer type 1 susceptibility protein (BRCA1)-associated protein 2 (BRAP or BRAP2). The central catalytic domain of BRAP comprises four subdomains: nucleotide-binding α/β plait (NBP), really interesting new gene (RING) zinc finger, ubiq...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1994
J Callis P Bedinger

Eukaryotic cells typically contain 0.2-1.0% of their total protein as the highly conserved protein ubiquitin, which exists both free and covalently attached to cellular proteins. The attachment of ubiquitin to cellular proteins occurs posttranslationally by a three-enzyme pathway and results in a peptide linkage of the C terminus of ubiquitin either to a lysyl epsilon-amino group of a substrate...

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