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Conformational proteomics of macromolecular architecture : approaching the structure of large molecular assemblies and their mechanisms of action /

Biological processes involving large macromolecular assemblies arethought to be a dynamic consequence of cooperativity andmetastability. The folding of a peptide chain creates localenvironments from which "activity" can emerge. In the same way, theassembly of large molecular complexes crea...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Cheng, R. Holland, Hammar, Lena
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Singapore ; River Edge, NJ : World Scientific Pub., ©2004.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Conformational proteomics of macromolecular architecture :  |b approaching the structure of large molecular assemblies and their mechanisms of action /  |c R. Holland Cheng & Lena Hammar, editors. 
260 |a Singapore ;  |a River Edge, NJ :  |b World Scientific Pub.,  |c ©2004. 
300 |a 1 online resource (xi, 420 pages) :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
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504 |a Includes bibliographical references and index. 
588 0 |a Print version record. 
505 0 |a Conformational Proteomics of Macromolecular Architecture: Approaching the Structure of Large Molecular Assemblies and Their Mechanisms of Action; PREFACE; Dynamic Architectures; The Theory of Quasi-equivalence; Approaching Large Assemblies in Membranes; Protein Shuttle; Molecular Machines; Conformational Proteomics; Acknowledgements; CONTENTS; Chapter 1. Early Theories of Virus Structure; Chapter 2. Quasi-Equivalence and Adaptability in Living Molecular Assemblies; Chapter 3. The Role of Disordered Segments in Viral Coat Proteins. 
520 |a Biological processes involving large macromolecular assemblies arethought to be a dynamic consequence of cooperativity andmetastability. The folding of a peptide chain creates localenvironments from which "activity" can emerge. In the same way, theassembly of large molecular complexes creates dynamic features thatwould only be feasible in a large construct. The biologicalimplications of such adaptation will be explored as it applies to thestatic quasisymmetry situations, as well as to the dynamics ofstructural transitions. The current wealth of solved high-resolutioncomplex structures makes th 
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650 0 |a Macromolecules  |x Structure. 
650 0 |a Biological systems. 
650 0 |a Proteomics. 
650 0 |a Structure-activity relationships (Biochemistry) 
650 1 2 |a Macromolecular Substances 
650 1 2 |a Molecular Conformation 
650 2 |a Proteomics 
650 2 2 |a Proteomics  |x methods 
650 2 2 |a Structure-Activity Relationship 
650 6 |a Systèmes biologiques. 
650 6 |a Protéomique. 
650 6 |a Relations structure-activité (Biochimie) 
650 7 |a SCIENCE  |x Chemistry  |x Organic.  |2 bisacsh 
650 7 |a Structure-activity relationships (Biochemistry)  |2 fast 
650 7 |a Biological systems  |2 fast 
650 7 |a Macromolecules  |x Structure  |2 fast 
650 7 |a Proteomics  |2 fast 
700 1 |a Cheng, R. Holland. 
700 1 |a Hammar, Lena. 
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