The conformation of end-groups is one determinant of carotenoid topology suitable for high fidelity molecular recognition: A study of beta- and epsilon-end-groups Article

Landrum, John T, Chatfield, David C, Mebel, Alex M et al. (2010). The conformation of end-groups is one determinant of carotenoid topology suitable for high fidelity molecular recognition: A study of beta- and epsilon-end-groups . ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 493(2), 169-174. 10.1016/j.abb.2009.10.007

cited authors

  • Landrum, John T; Chatfield, David C; Mebel, Alex M; Alvarez-Calderon, Francesca; Fernandez, Melissa V

sustainable development goals

authors

publication date

  • January 15, 2010

webpage

published in

keywords

  • BACTERIORHODOPSIN
  • BINDING
  • Biochemistry & Molecular Biology
  • Biophysics
  • CHROMOPHORE
  • CYCLOHEXENE RING
  • Carotenoids
  • Conformation
  • DEUTERIUM NMR
  • LIGHT-HARVESTING COMPLEX
  • LUTEIN
  • Life Sciences & Biomedicine
  • Lutein
  • PROTEIN
  • RHODOPSIN
  • Rotational barrier
  • Science & Technology
  • Selective binding
  • XANTHOPHYLLS
  • Zeaxanthin
  • beta-lonone ring
  • epsilon-lonone ring

Digital Object Identifier (DOI)

publisher

  • ELSEVIER SCIENCE INC

start page

  • 169

end page

  • 174

volume

  • 493

issue

  • 2