Methods in protein design

Salvato in:
Dettagli Bibliografici
Autore principale: Keating, Amy E.
Natura: Livre numérique
Lingua:Anglais
Pubblicazione: Amsterdam : Elsevier B. V. 2013.
Serie:Methods in enzymology 523
Accesso online:Accès Université d'Orléans et IFPM
Accès INSA CVL
Nota: Description d'après la consultation du 2013-10-17
Titre provenant de la page de titre du document numérique
Version électronique de l'édition de : San Diego, CA : Academic Press, 2013
La pagination de l'édition imprimée correspondante est de 538 p.
Cyberlibris (ScholarVox) corpus Sciences de l'ingénieur
Cyberlibris (ScholarVox) corpus Sciences de l'ingénieur
Type of computer file: 26 fichiers au format HTML et au format PDF
Autres localisations: Voir dans le Sudoc
Edition sous un autre format:• Methods in protein design, edited by Amy E. Keating, San Diego (Calif.), Academic Press/Elsevier, 2013, 1 vol. (liv-464 p.), Methods in enzymology, 978-0-12-394292-0
Sommario:
  • Computational design of novel protein binders and experimental affinity maturation
  • Mining tertiary structural motifs for assessment of designability
  • Computational methods for controlling binding specificity
  • Flexible backbone sampling methods to model and design protein alternative conformations
  • Osprey: protein design with ensembles, flexibility, and provable algorithms
  • Scientific benchmarks for guiding macromolecular energy function improvement
  • Molecular dynamics simulations for the ranking, evaluation, and refinement of computationally designed proteins
  • Multistate protein design using CLEVER and CLASSY
  • Using analyses of amino acid coevolution to understand protein structure and function
  • Evolution-based design of proteins
  • Protein engineering and stabilization from sequence statistics: variation and covariation analysis
  • Enzyme engineering by targeted libraries
  • Generation of high-performance binding proteins for pepetide motifs by affinity clamping
  • Engineering fibronectin-based binding proteins by yeast surface display
  • Engineering and analysis of peptide-recognition domain specificities by phage display and deep sequencing
  • Efficient sampling of SCHEMA chimera families to identify useful sequence elements
  • Protein switch engineering by domain insertion
  • Design of chimeric proteins by combination of subdomain-sized fragments
  • [alpha]-helix mimicry with [alpha/beta]-peptides
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