نتایج جستجو برای: ناحیه pdz

تعداد نتایج: 27011  

2016
Claire D. James Sally Roberts

Many of the human viruses with oncogenic capabilities, either in their natural host or in experimental systems (hepatitis B and C, human T cell leukaemia virus type 1, Kaposi sarcoma herpesvirus, human immunodeficiency virus, high-risk human papillomaviruses and adenovirus type 9), encode in their limited genome the ability to target cellular proteins containing PSD95/ DLG/ZO-1 (PDZ) interactio...

Journal: :Biochemical and biophysical research communications 2011
Jun Hyuck Lee Hajeung Park Soo Jeong Park Hak Jun Kim Soo Hyun Eom

The PDZ domain of the shank protein interacts with numerous cell membrane receptors and cytosolic proteins via the loosely defined binding motif X-(Ser/Thr)-X-Φ-COOH (Φ represents hydrophobic residues) at the carboxyl terminus of its target protein. This enables shank to serve as a membrane-associated scaffold for the assembly of signaling complexes. As the list of proteins that bind to the sha...

2014
Carola Bauch Judith Koliwer Friedrich Buck Hans-Hinrich Hönck Hans-Jürgen Kreienkamp

PSD-95/discs large/ZO-1 (PDZ) domain proteins integrate many G-protein coupled receptors (GPCRs) into membrane associated signalling complexes. Additional PDZ proteins are involved in intracellular receptor trafficking. We show that three PDZ proteins (SNX27, PIST and NHERF1/3) regulate the mouse somatostatin receptor subtype 5 (SSTR5). Whereas the PDZ ligand motif of SSTR5 is not necessary for...

Journal: :Biochemistry 2007
Matthew S Kelker Barbara Dancheck Tingting Ju Rene P Kessler Jebecka Hudak Angus C Nairn Wolfgang Peti

Neurabin and spinophilin are neuronal scaffolding proteins that play important roles in the regulation of synaptic transmission through their ability to target protein phosphatase 1 (PP1) to dendritic spines where PP1 dephosphorylates and inactivates glutamate receptors. However, thus far, it is still unknown how neurabin and spinophilin themselves are targeted to these membrane receptors. Spin...

Journal: :Biochemistry 2002
Georg Lamprecht Andreas Heil Susannah Baisch Elena Lin-Wu C Chris Yun Hubert Kalbacher Michael Gregor Ursula Seidler

Intestinal electroneutral NaCl absorption is mediated by parallel operation of Na(+)/H(+) and Cl(-)/HCO(3)(-) exchange in the enterocyte apical membrane. The ion transporters involved are Na(+)/H(+) exchanger 3 (NHE3) and the down regulated in adenoma (dra) gene product. cAMP-mediated inhibition of NHE3 requires the transporter to bind to the second PDZ (PSD95, disk large, ZO1) domain of the ad...

Journal: :The journal of physical chemistry. B 2007
Fabio Cecconi Paolo De Los Rios Francesco Piazza

PDZ domains are typical examples of binding motifs mediating the formation of protein-protein assemblies in many different cells. A quantitative characterization of the mechanisms intertwining structure, chemistry, and dynamics with the PDZ function represent a challenge in molecular biology. Here, we investigated the influence of native state topology on the thermodynamics and dissociation kin...

2016
Kenneth R. Maksimchuk Katherine A. Alser Rui Mou Raphael H. Valdivia Dewey G. McCafferty David M. Ojcius

The need for more effective anti-chlamydial therapeutics has sparked research efforts geared toward further understanding chlamydial pathogenesis mechanisms. Recent studies have implicated the secreted chlamydial serine protease, chlamydial protease-like activity factor (CPAF) as potentially important for chlamydial pathogenesis. By mechanisms that remain to be elucidated, CPAF is directed to a...

Journal: :Neuron 2005
Kate Prybylowski Kai Chang Nathalie Sans Lilly Kan Stefano Vicini Robert J. Wenthold

The NMDA receptor (NMDAR) is a component of excitatory synapses and a key participant in synaptic plasticity. We investigated the role of two domains in the C terminus of the NR2B subunit--the PDZ binding domain and the clathrin adaptor protein (AP-2) binding motif--in the synaptic localization of NMDA receptors. NR2B subunits lacking functional PDZ binding are excluded from the synapse. Mutati...

2016
Antonio Luis Egea-Jimenez Rodrigo Gallardo Abel Garcia-Pino Ylva Ivarsson Anna Maria Wawrzyniak Rudra Kashyap Remy Loris Joost Schymkowitz Frederic Rousseau Pascale Zimmermann

PDZ domain-containing proteins work as intracellular scaffolds to control spatio-temporal aspects of cell signalling. This function is supported by the ability of their PDZ domains to bind other proteins such as receptors, but also phosphoinositide lipids important for membrane trafficking. Here we report a crystal structure of the syntenin PDZ tandem in complex with the carboxy-terminal fragme...

Journal: :Science 1999
B J Hillier K S Christopherson K E Prehoda D S Bredt W A Lim

The PDZ protein interaction domain of neuronal nitric oxide synthase (nNOS) can heterodimerize with the PDZ domains of postsynaptic density protein 95 and syntrophin through interactions that are not mediated by recognition of a typical carboxyl-terminal motif. The nNOS-syntrophin PDZ complex structure revealed that the domains interact in an unusual linear head-to-tail arrangement. The nNOS PD...

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