The DEAD-Box Protein CYT-19 Uses Arginine Residuesin Its C-Tail To Tether RNA Substrates
The DEAD-Box Protein CYT-19 Uses Arginine Residuesin Its C-Tail To Tether RNA Substrates
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.7b00362/20170707/images/medium/bi-2017-00362h_0007.gif
Biochemistry
DOI: 10.1021/acs.biochem.7b00362
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[NMR paper] Unambiguous Determination of Protein Arginine Ionization States in Solution by NMR Spectroscopy.
Unambiguous Determination of Protein Arginine Ionization States in Solution by NMR Spectroscopy.
Unambiguous Determination of Protein Arginine Ionization States in Solution by NMR Spectroscopy.
Angew Chem Int Ed Engl. 2016 Nov 29;:
Authors: Yoshimura Y, Oktaviani NA, Yonezawa K, Kamikubo H, Mulder FA
Abstract
Because arginine residues in proteins are expected to be in their protonated form almost without exception, reports demonstrating that a protein arginine residue is charge-neutral are rare and potentially controversial....
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[NMR paper] Arginine-, D-arginine-vasopressin, and their inverso analogues in micellar and liposomic models of cell membrane: CD, NMR, and molecular dynamics studies.
Arginine-, D-arginine-vasopressin, and their inverso analogues in micellar and liposomic models of cell membrane: CD, NMR, and molecular dynamics studies.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--production.springer.de-OnlineResources-Logos-springerlink.gif http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/https:--www.ncbi.nlm.nih.gov-corehtml-pmc-pmcgifs-pubmed-pmc.gif Related Articles Arginine-, D-arginine-vasopressin, and their inverso analogues in micellar and liposomic models of cell membrane: CD, NMR, and molecular dynamics...
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Protein Arginine Methyltransferase 8: Tetrameric Structure and Protein Substrate Specificity
Protein Arginine Methyltransferase 8: Tetrameric Structure and Protein Substrate Specificity
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.5b00995/20151215/images/medium/bi-2015-00995k_0008.gif
Biochemistry
DOI: 10.1021/acs.biochem.5b00995
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pUL69 of Human Cytomegalovirus Recruits the Cellular Protein Arginine ... - Journal of Virology
pUL69 of Human Cytomegalovirus Recruits the Cellular Protein Arginine ... - Journal of Virology
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pUL69 of Human Cytomegalovirus Recruits the Cellular Protein Arginine ...
Journal of Virology
Remarkably, nuclear magnetic resonance (NMR) analyses revealed the same α-helical structures for pUL69 sequences encoding either the wild type R1/R2 boxes or a UAP56/PRMT6 binding-deficient derivative, thereby excluding the possibility that R/A ...
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Solution NMR Structure of the TatA Component of the Twin-Arginine Protein Transport S
Solution NMR Structure of the TatA Component of the Twin-Arginine Protein Transport System from Gram-Positive Bacterium Bacillus subtilis.
Related Articles Solution NMR Structure of the TatA Component of the Twin-Arginine Protein Transport System from Gram-Positive Bacterium Bacillus subtilis.
J Am Chem Soc. 2010 Aug 20;
Authors: Hu Y, Zhao E, Li H, Xia B, Jin C
The twin-arginine transport (Tat) system translocates folded proteins across the bacterial cytoplasmic or chloroplast thylakoid membrane of plants. The Tat system in most Gram-positive...
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08-25-2010 02:04 PM
[NMR paper] Purification of cloned trypanosomal calmodulin and preliminary NMR studies.
Purification of cloned trypanosomal calmodulin and preliminary NMR studies.
Related Articles Purification of cloned trypanosomal calmodulin and preliminary NMR studies.
J Chromatogr. 1991 Feb 22;539(2):501-5
Authors: Sweeney PJ, Walker JM, Reid DG, Elshourbagy N
Cloned trypanosomal calmodulin was expressed in Escherichia coli and purified to homogeneity using hydrophobic interaction chromatography on phenyl-Sepharose. The purified protein was subjected to NMR analysis which allows detailed changes to be observed when, firstly, calcium, and...
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Solution NMR Structure of the TatA Component of the Twin-Arginine Protein Transport S
Solution NMR Structure of the TatA Component of the Twin-Arginine Protein Transport System from Gram-Positive Bacterium Bacillus subtilis
Yunfei Hu et al
http://pubs.acs.org//appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja1053785/aop/images/medium/ja-2010-053785_0001.gifJournal of the American Chemical Society, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable).
Source: Journal of the American Chemical Society