نتایج جستجو برای: ناحیه pdz

تعداد نتایج: 27011  

Journal: :Assay and drug development technologies 2007
Xuesong Chen Jamie C Longgood Carolyn Michnoff Shuguang Wei Doug E Frantz Llya Bezprozvanny

Several hundred PDZ (postsynaptic density-95, Drosophila disks-large, ZO-1) domain-containing proteins have been identified in the human genome. PDZ domains play a critical role in organization and function of cellular signaling pathways. Thus, small molecule inhibitors of PDZ domain association with their targets have wide potential applications as research and therapeutic agents. PDZ domains ...

2016
Ward G Walkup Tara L Mastro Leslie T Schenker Jost Vielmetter Rebecca Hu Ariella Iancu Meera Reghunathan Barry Dylan Bannon Mary B Kennedy

SynGAP is a Ras/Rap GTPase-activating protein (GAP) that is a major constituent of postsynaptic densities (PSDs) from mammalian forebrain. Its α1 isoform binds to all three PDZ (PSD-95, Discs-large, ZO-1) domains of PSD-95, the principal PSD scaffold, and can occupy as many as 15% of these PDZ domains. We present evidence that synGAP-α1 regulates the composition of the PSD by restricting bindin...

Journal: :Acta biochimica Polonica 2003
Filip Jeleń Arkadiusz Oleksy Katarzyna Smietana Jacek Otlewski

PDZ domains are ubiquitous protein interaction modules that play a key role in cellular signaling. Their binding specificity involves recognition of the carboxyl-terminus of various proteins, often belonging to receptor and ion channel families. PDZ domains also mediate more complicated molecular networks through PDZ-PDZ interactions, recognition of internal protein sequences or phosphatidylino...

2006
Christine Alewine Olav Olsen James B. Wade Paul A. Welling Keith Mostov

PDZ proteins usually contain multiple protein–protein interaction domains and act as molecular scaffolds that are important for the generation and maintenance of cell polarity and cell signaling. Here, we identify and characterize TIP-1 as an atypical PDZ protein that is composed almost entirely of a single PDZ domain and functions as a negative regulator of PDZ-based scaffolding. We found that...

2016
Javier Murciano-Calles Jofre Güell-Bosch Sandra Villegas Jose C. Martinez

PDZ domains are protein-protein interaction modules sharing the same structural arrangement. To discern whether they display common features in their unfolding/misfolding behaviour we have analyzed in this work the unfolding thermodynamics, together with the misfolding kinetics, of the PDZ fold using three archetypical examples: the second and third PDZ domains of the PSD95 protein and the Erbi...

Journal: :The Journal of biological chemistry 2003
Young Jun Im Jun Hyuck Lee Seong Ho Park Soo Jeong Park Seong-Hwan Rho Gil Bu Kang Eunjoon Kim Soo Hyun Eom

The Shank/proline-rich synapse-associated protein family of multidomain proteins is known to play an important role in the organization of synaptic multiprotein complexes. For instance, the Shank PDZ domain binds to the C termini of guanylate kinase-associated proteins, which in turn interact with the guanylate kinase domain of postsynaptic density-95 scaffolding proteins. Here we describe the ...

2017
Majus Misiak Mateusz Heldt Marlena Szeligowska Stefania Mazzini Leonardo Scaglioni Grzegorz J. Grabe Marcin Serocki Jan Lica Marta Switalska Joanna Wietrzyk Giovanni L. Beretta Paola Perego Dominik Zietkowski Maciej Baginski Edward Borowski Andrzej Skladanowski

Anthrapyridazones, imino analogues of anthraquinone, constitute a family of compounds with remarkable anti-cancer activity. To date, over 20 derivatives were studied, of which most displayed nanomolar cytotoxicity towards broad spectrum of cancer cells, including breast, prostate and leukemic ones. BS-154, the most potent derivative, had IC50 values close to 1 nM, however, it was toxic in anima...

2014
Yi Mu Pengfei Cai Siqi Hu Sucan Ma Youhe Gao

Protein-protein interactions (PPIs) are essential events to play important roles in a series of biological processes. There are probably more ways of PPIs than we currently realized. Structural and functional investigations of weak PPIs have lagged behind those of strong PPIs due to technical difficulties. Weak PPIs are often short-lived, which may result in more dynamic signals with important ...

2015
Tatyana Mamonova Qiangmin Zhang Jahan Ali Khajeh Zimei Bu Alessandro Bisello Peter A. Friedman Peter Schuck

Na+/H+ Exchanger Regulatory Factor-1 (NHERF1) is a scaffolding protein containing 2 PDZ domains that coordinates the assembly and trafficking of transmembrane receptors and ion channels. Most target proteins harboring a C-terminus recognition motif bind more-or-less equivalently to the either PDZ domain, which contain identical core-binding motifs. However some substrates such as the type II so...

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