Jiafei Mao, Nhu-Nguyen Do, Frank Scholz, Lenica Reggie, Michaela Mehler, Andrea Lakatos, Yean-Sin Ong, Sandra J. Ullrich, Lynda J. Brown, Richard C. D. Brown, Johanna Becker-Baldus, Josef Wachtveitl and Clemens Glaubitz
Journal of the American Chemical Society
DOI: 10.1021/ja5097946
[NMR paper] The Structural Basis of the Green-Blue Color Switching in Proteorhodopsin determined by NMR Spectroscopy.
The Structural Basis of the Green-Blue Color Switching in Proteorhodopsin determined by NMR Spectroscopy.
The Structural Basis of the Green-Blue Color Switching in Proteorhodopsin determined by NMR Spectroscopy.
J Am Chem Soc. 2014 Nov 21;
Authors: Mao J, Do NN, Scholz F, Reggie L, Mehler M, Lakatos A, Ong YS, Ullrich SJ, Brown LJ, Brown RC, Becker-Baldus J, Wachtveitl J, Glaubitz C
Abstract
Proteorhodopsins (PRs) found in marine microbes are the most abundant retinal-based photoreceptors on this planet. PR variants show a high...
The EF Loop in Green Proteorhodopsin Affects Conformation and*Photocycle dynamics
From The DNP-NMR Blog:
The EF Loop in Green Proteorhodopsin Affects Conformation and*Photocycle dynamics
Mehler, M., et al., The EF Loop in Green Proteorhodopsin Affects Conformation and Photocycle dynamics. Biophysical Journal, 2013. 105(2): p. 385-397.
http://dx.doi.org/10.1016/j.bpj.2013.06.014
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08-16-2013 08:36 PM
Characterization of the ground state dynamics of proteorhodopsin by NMR and optical spectroscopies
Characterization of the ground state dynamics of proteorhodopsin by NMR and optical spectroscopies
Abstract We characterized the dynamics of proteorhodopsin (PR), solubilized in diC7PC, a detergent micelle, by liquid-state NMR spectroscopy at T = 323 K. Insights into the dynamics of PR at different time scales could be obtained and dynamic hot spots could be identified at distinct, functionally relevant regions of the protein, including the BC loop, the EF loop, the N-terminal part of helix F and the C-terminal part of helix G. We further characterize the dependence of the photocycle...
[NMR paper] Metal-ligand interplay in blue copper proteins studied by 1H NMR spectroscopy: Cu(II)
Metal-ligand interplay in blue copper proteins studied by 1H NMR spectroscopy: Cu(II)-pseudoazurin and Cu(II)-rusticyanin.
Related Articles Metal-ligand interplay in blue copper proteins studied by 1H NMR spectroscopy: Cu(II)-pseudoazurin and Cu(II)-rusticyanin.
J Am Chem Soc. 2002 Nov 20;124(46):13698-708
Authors: Donaire A, Jiménez B, Fernández CO, Pierattelli R, Niizeki T, Moratal JM, Hall JF, Kohzuma T, Hasnain SS, Vila AJ
The blue copper proteins (BCPs), pseudoazurin from Achromobacter cycloclastes and rusticyanin from Thiobacillus...
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11-24-2010 08:58 PM
[NMR paper] The solution NMR structure of a blue-green algae hepatotoxin, microcystin-RR--a compa
The solution NMR structure of a blue-green algae hepatotoxin, microcystin-RR--a comparison with the structure of microcystin-LR.
Related Articles The solution NMR structure of a blue-green algae hepatotoxin, microcystin-RR--a comparison with the structure of microcystin-LR.
Eur J Biochem. 1998 Dec 1;258(2):301-12
Authors: Trogen GB, Edlund U, Larsson G, Sethson I
The microcystin-RR structures are compared with the structures of microcystin-LR in solution as well as in the crystal structure of the complex with protein phosphatase. The gross...
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11-17-2010 11:15 PM
[NMR paper] NMR structures of a mitochondrial transit peptide from the green alga Chlamydomonas r
NMR structures of a mitochondrial transit peptide from the green alga Chlamydomonas reinhardtii.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles NMR structures of a mitochondrial transit peptide from the green alga Chlamydomonas reinhardtii.
FEBS Lett. 1996 Aug 5;391(1-2):203-8
Authors: Lancelin JM, Gans P, Bouchayer E, Bally I, Arlaud GJ, Jacquot JP
The 26-amino-acid pre-sequence of the ATP synthase beta subunit that directs the protein from the cytosol to...