نتایج جستجو برای: oligomerization

تعداد نتایج: 7072  

2016
Camille Sayou Max H. Nanao Marc Jamin David Posé Emmanuel Thévenon Laura Grégoire Gabrielle Tichtinsky Grégoire Denay Felix Ott Marta Peirats Llobet Markus Schmid Renaud Dumas François Parcy

Deciphering the mechanisms directing transcription factors (TFs) to specific genome regions is essential to understand and predict transcriptional regulation. TFs recognize short DNA motifs primarily through their DNA-binding domain. Some TFs also possess an oligomerization domain suspected to potentiate DNA binding but for which the genome-wide influence remains poorly understood. Here we focu...

Journal: :Journal of virology 2001
R Sundararajan E White

Tumor necrosis factor alpha (TNF-alpha)-mediated death signaling causes the recruitment of monomeric pro- apoptotic Bax into a 500-kDa protein complex. The adenovirus Bcl-2 homologue, E1B 19K, inhibits TNF-alpha-mediated apoptosis, interacts with Bax, and blocked the formation of the 500-kDa Bax complex. TNF-alpha and truncated Bid induced Bax-Bax cross-linking, indicative of oligomerization, a...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Diana Pendin Jessica Tosetto Tyler J Moss Camilla Andreazza Stefano Moro James A McNew Andrea Daga

The mechanisms governing atlastin-mediated membrane fusion are unknown. Here we demonstrate that a three-helix bundle (3HB) within the middle domain is required for oligomerization. Mutation of core hydrophobic residues within these helices inactivates atlastin function by preventing membrane tethering and the subsequent fusion. GTP binding induces a conformational change that reorients the GTP...

Journal: :The Journal of Cell Biology 2004
Simona Paladino Daniela Sarnataro Rudolf Pillich Simona Tivodar Lucio Nitsch Chiara Zurzolo

An essential but insufficient step for apical sorting of glycosylphosphatidylinositol (GPI)-anchored proteins (GPI-APs) in epithelial cells is their association with detergent-resistant microdomains (DRMs) or rafts. In this paper, we show that in MDCK cells both apical and basolateral GPI-APs associate with DRMs during their biosynthesis. However, only apical and not basolateral GPI-APs are abl...

Journal: :The Journal of biological chemistry 1999
I Biswas C Ban K G Fleming J Qin J W Lary D A Yphantis W Yang P Hsieh

The MutS DNA mismatch protein recognizes heteroduplex DNAs containing mispaired or unpaired bases. We have examined the oligomerization of a MutS protein from Thermus aquaticus that binds to heteroduplex DNAs at elevated temperatures. Analytical gel filtration, cross-linking of MutS protein with disuccinimidyl suberate, light scattering, and matrix-assisted laser desorption/ionization time-of-f...

Journal: :FEBS letters 2009
Mayuko Okabe Tohru Minamino Katsumi Imada Keiichi Namba May Kihara

FliI, the ATPase involved in bacterial flagellar protein export, forms a complex with its regulator FliH in the cytoplasm and hexamerizes upon docking to the export gate composed of integral membrane proteins. The extreme N-terminal region of FliI is involved not only in its interaction with FliH but also in its oligomerization, but the regulatory mechanism of oligomerization remains unclear. U...

Journal: :The Journal of biological chemistry 2004
Koh Takeuchi Hideo Takahashi Mariko Sugai Hideo Iwai Toshiyuki Kohno Kazuhisa Sekimizu Shunji Natori Ichio Shimada

The action mechanism of sapecin, an antibacterial peptide with membrane permeabilization activity, was investigated. The dose dependence of the membrane permeabilization caused by sapecin was sigmoidal, suggesting that sapecin oligomerization leads to the membrane permeabilization. Solution nuclear magnetic resonance analysis of the sapecin-phospholipid vesicle complex revealed the surface buri...

2013
Sayan Mondal Jennifer M. Johnston Hao Wang George Khelashvili Marta Filizola Harel Weinstein

Spatial organization of G-protein coupled receptors (GPCRs) into dimers and higher order oligomers has been demonstrated in vitro and in vivo. The pharmacological readout was shown to depend on the specific interfaces, but why particular regions of the GPCR structure are involved, and how ligand-determined states change them remains unknown. Here we show why protein-membrane hydrophobic matchin...

Journal: :The EMBO journal 2009
Qian Cheng Lihong Chen Zhenyu Li William S Lane Jiandong Chen

Rapid activation of p53 by ionizing irradiation is a classic DNA damage response mediated by the ATM kinase. However, the major signalling target and mechanism that lead to p53 stabilization are unknown. We show in this report that ATM induces p53 accumulation by phosphorylating the ubiquitin E3 ligase MDM2. Multiple ATM target sites near the MDM2 RING domain function in a redundant manner to p...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Tina Perica Cyrus Chothia Sarah A Teichmann

Oligomerization plays an important role in the function of many proteins. Thus, understanding, predicting, and, ultimately, engineering oligomerization presents a long-standing interest. From the perspective of structural biology, protein-protein interactions have mainly been analyzed in terms of the biophysical nature and evolution of protein interfaces. Here, our aim is to quantify the import...

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