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Monotopic Membrane Proteins Join the Fold.
Allen, Karen N; Entova, Sonya; Ray, Leah C; Imperiali, Barbara.
Afiliación
  • Allen KN; Department of Chemistry, Boston University, Boston, MA 02215, USA; Program in Biomolecular Pharmacology, Boston University School of Medicine, Boston, MA 02118, USA. Electronic address: drkallen@bu.edu.
  • Entova S; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Ray LC; Program in Biomolecular Pharmacology, Boston University School of Medicine, Boston, MA 02118, USA.
  • Imperiali B; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. Electronic address: imper@mit.edu.
Trends Biochem Sci ; 44(1): 7-20, 2019 01.
Article en En | MEDLINE | ID: mdl-30337134
ABSTRACT
Monotopic membrane proteins, classified by topology, are proteins that embed into a single face of the membrane. These proteins are generally underrepresented in the Protein Data Bank (PDB), but the past decade of research has revealed new examples that allow the description of generalizable features. This Opinion article summarizes shared characteristics including oligomerization states, modes of membrane association, mechanisms of interaction with hydrophobic or amphiphilic substrates, and homology to soluble folds. We also discuss how associations of monotopic enzymes in pathways can be used to promote substrate specificity and product composition. These examples highlight the challenges in structure determination specific to this class of proteins, but also the promise of new understanding from future study of these proteins that reside at the interface.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas de la Membrana Límite: Animals / Humans Idioma: En Revista: Trends Biochem Sci Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas de la Membrana Límite: Animals / Humans Idioma: En Revista: Trends Biochem Sci Año: 2019 Tipo del documento: Article