Repairing oxidized proteins in the bacterial envelope using respiratory chain ... Nature.com
Consistently, MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation, including the primary periplasmic chaperone SurA ...
Repairing oxidized proteins in the bacterial envelope using respiratory chain ... - Nature.com
Repairing oxidized proteins in the bacterial envelope using respiratory chain ... - Nature.com
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Repairing oxidized proteins in the bacterial envelope using respiratory chain ...
Nature.com
The reactive species of oxygen and chlorine damage cellular components, potentially leading to cell death. In proteins, the sulfur-containing amino acid methionine is converted to methionine sulfoxide, which can cause a loss...
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Protein–protein interaction in Rhodothermus marinus respiratory chain studied by NMR spectroscopy
Protein–protein interaction in Rhodothermus marinus respiratory chain studied by NMR spectroscopy
Publication date: July 2014
Source:Biochimica et Biophysica Acta (BBA) - Bioenergetics, Volume 1837, Supplement</br>
Author(s): Filipa Calisto , Patricia N. Refojo , Miguel Teixeira , Ricardo O. Louro , Manuela M. Pereira</br>
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06-26-2014 08:53 AM
Newly Discovered Molecule Cuts Bacterial Proteins Short - The Biological SCENE
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Newly Discovered Molecule Cuts Bacterial Proteins Short
The Biological SCENE
With additional separations, they isolated the active compound and determined the structure using nuclear magnetic resonance spectroscopy. The compound included a collage of functional groups, but its unique feature was an orthoformate moietyâ??a trio ...
Newly Discovered Molecule Cuts Bacterial Proteins Short - The Biological SCENE
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08-09-2013 04:40 AM
[NMR paper] Study of ion translocation by respiratory complex I. A new insight using (23)Na NMR spectroscopy.
Study of ion translocation by respiratory complex I. A new insight using (23)Na NMR spectroscopy.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles Study of ion translocation by respiratory complex I. A new insight using (23)Na NMR spectroscopy.
Biochim Biophys Acta. 2012 Oct;1817(10):1810-6
Authors: Batista AP, Marreiros BC, Louro RO, Pereira MM
Abstract
The research on complex I has gained recently a new enthusiasm, especially after the resolution...
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05-04-2013 09:18 PM
‘q-titration’ of long-chain and short-chain lipids differentiates between structured and mobile residues of membrane proteins studied in bicelles by solution NMR spectroscopy
‘q-titration’ of long-chain and short-chain lipids differentiates between structured and mobile residues of membrane proteins studied in bicelles by solution NMR spectroscopy
Publication year: 2011
Source: Journal of Magnetic Resonance, Available online 25 October 2011</br>
Woo Sung*Son, Sang Ho*Park, Henry J.*Nothnagel, George J.*Lu, Yan*Wang, ...</br>
‘q-titration’ refers to the systematic comparison of signal intensities in solution NMR spectra of uniformlyN labeled membrane proteins solubilized in micelles and isotropic bicelles as a function of the molar ratios (q) of the...
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[NMR paper] Conformational study of fragments of envelope proteins (gp120: 254-274 and gp41: 519-
Conformational study of fragments of envelope proteins (gp120: 254-274 and gp41: 519-541) of HIV-1 by NMR and MD simulations.
Related Articles Conformational study of fragments of envelope proteins (gp120: 254-274 and gp41: 519-541) of HIV-1 by NMR and MD simulations.
J Pept Sci. 2004 Jun;10(6):363-80
Authors: Kanyalkar M, Srivastava S, Saran A, Coutinho E
The envelope proteins, gp 120 and gp41 of HIV-1, play a crucial role in receptor (CD4+ lymphocytes) binding and membrane fusion. The fragment 254-274 of gp120 is conserved in all strains of...
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[NMR paper] Comparison of backbone and tryptophan side-chain dynamics of reduced and oxidized Esc
Comparison of backbone and tryptophan side-chain dynamics of reduced and oxidized Escherichia coli thioredoxin using 15N NMR relaxation measurements.
Related Articles Comparison of backbone and tryptophan side-chain dynamics of reduced and oxidized Escherichia coli thioredoxin using 15N NMR relaxation measurements.
Biochemistry. 1993 Jan 19;32(2):426-35
Authors: Stone MJ, Chandrasekhar K, Holmgren A, Wright PE, Dyson HJ
The backbone and tryptophan side-chain dynamics of both the reduced and oxidized forms of uniformly 15N-labeled Escherichia...