نتایج جستجو برای: ligases

تعداد نتایج: 3608  

Journal: :The Plant cell 2004
Suhua Feng Yunping Shen James A Sullivan Vicente Rubio Yue Xiong Tai-ping Sun Xing Wang Deng

Ubiquitin/proteasome-mediated protein degradation controls various developmental pathways in eukaryotes. Cullin-containing complexes are both versatile and abundant groups of RING family ubiquitin E3 ligases, whose activities are subject to control by RUB/Nedd8 (for related to ubiquitin/neural precursor cell-expressed developmentally downregulated 8) modification of their cullin subunits. Here,...

2018
Youngeun Kim Eek-hoon Jho

The Hippo signaling pathway plays an essential role in adult tissue homeostasis and organ size control. Abnormal regulation of Hippo signaling can be a cause for multiple types of human cancers. Since the awareness of the importance of the Hippo signaling in a wide range of biological fields has been continually grown, it is also understood that a thorough and well-rounded comprehension of the ...

Journal: :Current Biology 2010
Swati Suryavanshi Bernard Eddé Laura A. Fox Stella Guerrero Robert Hard Todd Hennessey Amrita Kabi David Malison David Pennock Winfield S. Sale Dorota Wloga Jacek Gaertig

How microtubule-associated motor proteins are regulated is not well understood. A potential mechanism for spatial regulation of motor proteins is provided by posttranslational modifications of tubulin subunits that form patterns on microtubules. Glutamylation is a conserved tubulin modification [1] that is enriched in axonemes. The enzymes responsible for this posttranslational modification, gl...

Journal: :Journal of cell science 2006
Alison Reindle Irina Belichenko Gwendolyn R Bylebyl Xiaole L Chen Nishant Gandhi Erica S Johnson

Saccharomyces cerevisiae contains two Siz/PIAS SUMO E3 ligases, Siz1 and Siz2/Nfi1, and one other known ligase, Mms21. Although ubiquitin ligases are highly substrate-specific, the degree to which SUMO ligases target distinct sets of substrates is unknown. Here we show that although Siz1 and Siz2 each have unique substrates in vivo, sumoylation of many substrates can be stimulated by either pro...

2012
Jennifer R. Kowalski Peter Juo

Posttranslational modification of proteins by ubiquitin has emerged as a critical regulator of synapse development and function. Ubiquitination is a reversible modification mediated by the concerted action of a large number of specific ubiquitin ligases and ubiquitin proteases, called deubiquitinating enzymes (DUBs). The balance of activity of these enzymes determines the localization, function...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Michelle Harreman Michael Taschner Stefan Sigurdsson Roy Anindya James Reid Baggavalli Somesh Stephanie E Kong Charles A S Banks Ronald C Conaway Joan W Conaway Jesper Q Svejstrup

The proteasome degrades proteins modified by polyubiquitylation, so correctly controlled ubiquitylation is crucial to avoid unscheduled proteolysis of essential proteins. The mechanism regulating proteolysis of RNAPII has been controversial since two distinct ubiquitin ligases (E3s), Rsp5 (and its human homologue NEDD4) and Elongin-Cullin complex, have both been shown to be required for its DNA...

2014
Peter Canning Alex N. Bullock

E3 ubiquitin ligases that direct substrate proteins to the ubiquitin-proteasome system are promising, though largely unexplored drug targets both because of their function and their remarkable specificity. CRLs [Cullin-RING (really interesting new gene) ligases] are the largest group of E3 ligases and function as modular multisubunit complexes constructed around a Cullin-family scaffold protein...

2014
Barbara Mojsa Iréna Lassot Solange Desagher

Mcl-1 is an anti-apoptotic protein of the Bcl-2 family that is essential for the survival of multiple cell lineages and that is highly amplified in human cancer. Under physiological conditions, Mcl-1 expression is tightly regulated at multiple levels, involving transcriptional, post-transcriptional and post-translational processes. Ubiquitination of Mcl-1, that targets it for proteasomal degrad...

2017
Masaaki Okamoto Takahisa Kouwaki Yoshimi Fukushima Hiroyuki Oshiumi

RIG-I is a pattern recognition receptor and recognizes cytoplasmic viral double-stranded RNA (dsRNA). Influenza A virus, hepatitis C virus, and several other pathogenic viruses are mainly recognized by RIG-I, resulting in the activation of the innate immune responses. The protein comprises N-terminal two caspase activation and recruitment domains (2CARDs), an RNA helicase domain, and the C-term...

Journal: :Molecular Systems Biology 2009
Avinash Persaud Philipp Alberts Eva M Amsen Xuejian Xiong James Wasmuth Zachary Saadon Chris Fladd John Parkinson Daniela Rotin

Target recognition by the ubiquitin system is mediated by E3 ubiquitin ligases. Nedd4 family members are E3 ligases comprised of a C2 domain, 2-4 WW domains that bind PY motifs (L/PPxY) and a ubiquitin ligase HECT domain. The nine Nedd4 family proteins in mammals include two close relatives: Nedd4 (Nedd4-1) and Nedd4L (Nedd4-2), but their global substrate recognition or differences in substrate...

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