Protein-Protein Interactions as New Drug Targets

Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Klussmann, Enno. (Editor), Scott, John. (Editor)
Format: eBook
Language:English
Published: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2008.
Edition:1st ed. 2008.
Series:Handbook of Experimental Pharmacology, 186
Subjects:
Online Access:https://doi.org/10.1007/978-3-540-72843-6
Table of Contents:
  • Organization of Scaffolds
  • A-Kinase Anchoring Proteins as the Basis for cAMP Signaling
  • Arrestins as Multi-Functional Signaling Adaptors
  • Role of Ena/VASP Proteins in Homeostasis and Disease
  • Scaffold/Matrix Attachment Regions (S/MARs): Relevance for Disease and Therapy
  • Clathrin/AP-2-Dependent Endocytosis: A Novel Playground for the Pharmacological Toolbox?
  • Scaffolding Proteins and Cellular Signalling
  • PDE4 Associates with Different Scaffolding Proteins: Modulating Interactions as Treatment for Certain Diseases
  • G-Protein-Coupled Receptor-Signaling Components in Membrane Raft and Caveolae Microdomains
  • Protein Scaffolds, Lipid Domains and Substrate Recognition in Protein Kinase C Function: Implications for Rational Drug Design
  • Compartmentalised MAPK Pathways
  • Dynamic Protein Complexes Regulate NF-?B Signaling
  • An Oncogenic Hub: ?-Catenin as a Molecular Target for Cancer Therapeutics
  • A Toolkit for Real-Time Detection of cAMP: Insights into Compartmentalized Signaling
  • Cell Type-Specific Anchoring
  • Scaffolding Proteins in Cardiac Myocytes
  • Molecular Architecture of Signal Complexes Regulating Immune Cell Function
  • Scaffolding Proteins at the Postsynaptic Density: Shank as the Architectural Framework
  • Interference with Protein-Protein Interaction Sites as a New Pharmacological Concept
  • Domains Mediate Protein-Protein Interactions and Nucleate Protein Assemblies
  • Proline-Rich Sequence Recognition Domains (PRD): Ligands, Function and Inhibition
  • Chemical Inhibition Through Conformational Stabilization of Rho GTPase Effectors
  • Pharmacological Interference with Protein-Protein Interactions Mediated by Coiled-Coil Motifs
  • Direct AKAP-Mediated Protein-Protein Interactions as Potential Drug Targets.