نتایج جستجو برای: ubd

تعداد نتایج: 191  

Journal: :Cell 2013
Yifat Merbl Phillipe Refour Hevan Patel Michael Springer Marc W. Kirschner

Ubiquitin and ubiquitin-like (Ubl) protein modifications affect protein stability, activity, and localization, but we still lack broad understanding of the functions of Ubl modifications. We have profiled the protein targets of ubiquitin and six additional Ubls in mitosis using a functional assay that utilizes active mammalian cell extracts and protein microarrays and identified 1,500 potential...

2016
Yong Xu Yin Yao Shugart Guoqiang Wang Zaohuo Cheng Chunhui Jin Kai Zhang Jun Wang Hao Yu Weihua Yue Fuquan Zhang Dai Zhang

To identify gene expression abnormalities in schizophrenia (SZ), we generated whole-genome gene expression profiles using microarrays on peripheral blood mononuclear cells (PBMCs) from 18 early-onset SZ cases and 12 controls. We detected 84 transcripts differentially expressed by diagnostic status, with 82 genes being upregulated and 2 downregulated. We identified two SZ associated gene coexpre...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
N Agell U Bond M J Schlesinger

Ubiquitin, a highly conserved protein of 76 amino acids found in all eukaryotes, is translated from mRNAs that contain either multiple, contiguous coding sequences of the protein or a single ubiquitin coding sequence fused to sequences coding for 52 or 76 amino acids. We describe here formation of monoubiquitin from in vitro translation of mRNAs containing either two complete sequences or one c...

2015
Yosua Adi Kristariyanto Soo-Youn Choi Syed Arif Abdul Rehman Maria Stella Ritorto David G Campbell Nicholas A Morrice Rachel Toth Yogesh Kulathu

Ubiquitylation regulates a multitude of biological processes and this versatility stems from the ability of ubiquitin (Ub) to form topologically different polymers of eight different linkage types. Whereas some linkages have been studied in detail, other linkage types including Lys33-linked polyUb are poorly understood. In the present study, we identify an enzymatic system for the large-scale a...

2012
Samuel Buchsbaum Beatrice Bercovich Aaron Ciechanover

FAT10 is a ubiquitin-like protein modifier that is induced in vertebrates following certain inflammatory stimuli. Its functions and the repertoire of its target substrates have remained elusive. In contrast to ubiquitin, its cellular abundance is tightly controlled by both transcriptional and posttranslational regulation, and it was reported to be rapidly degraded by the proteasome. Here we pro...

2014
Ai-Xin Song Hui Yang Yong-Guang Gao Chen-Jie Zhou Yu-Hang Zhang Hong-Yu Hu

The ubiquitination levels of protein substrates in eukaryotic cells are delicately orchestrated by various protein cofactors and enzymes. Dendritic cell-derived ubiquitin (Ub)-like protein (DC-UbP), also named as Ub domain-containing protein 2 (UBTD2), is a potential Ub shuttle protein comprised of a Ub-like (UbL) domain and a Ub-binding domain (UBD), but its biological function remains largely...

Journal: :FEBS letters 2009
Gunter Schmidtke Birte Kalveram Marcus Groettrup

The ubiquitin-like modifier FAT10 targets proteins for degradation by the proteasome, a process accelerated by the UBL-UBA domain protein NEDD8 ultimate buster 1-long. Here, we show that FAT10-mediated degradation occurs independently of poly-ubiquitylation as purified 26S proteasome readily degraded FAT10-dihydrofolate reductase (DHFR) but not ubiquitin-DHFR in vitro. Interestingly, the 26S pr...

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