[NMR paper] STD NMR Epitope Perturbation by Mutation Unveils the Mechanism of YM155 as an Arginine-Glycosyltransferases Inhibitor Effective in Treating Enteropathogenic Diseases
STD NMR Epitope Perturbation by Mutation Unveils the Mechanism of YM155 as an Arginine-Glycosyltransferases Inhibitor Effective in Treating Enteropathogenic Diseases
Enteropathogenic arginine-glycosyltransferases (Arg-GTs) alter higher eukaryotic proteins by attaching a GlcNAc residue to arginine acceptor sites, disrupting essential pathways such as NF-?B signaling, which promotes bacterial survival. These enzymes are potential drug targets for treating related diseases. In this study, we present a novel STD NMR Epitope Perturbation by Mutation spectroscopic approach that, in combination with hydrogen-deuterium exchange mass spectrometry (HDX-MS), and...
[NMR paper] NMR structure of emfourin, a novel protein metalloprotease inhibitor: insights into the mechanism of action
NMR structure of emfourin, a novel protein metalloprotease inhibitor: insights into the mechanism of action
Emfourin (M4in) is a protein metalloprotease inhibitor recently discovered in the bacterium Serratia proteamaculans and the prototype of a new family of protein protease inhibitors with an unknown mechanism of action. Protealysin-like proteases (PLPs) of the thermolysin family are natural targets of emfourin-like inhibitors (ELIs) widespread in bacteria and known in archaea. The available data indicate the involvement of PLPs in interbacterial interaction as well as bacterial...
[ASAP] Characterization of the Kinetic Mechanism of Human Protein Arginine Methyltransferase 5
Characterization of the Kinetic Mechanism of Human Protein Arginine Methyltransferase 5
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.0c00554/20201204-01/images/medium/bi0c00554_0006.gif
Biochemistry
DOI: 10.1021/acs.biochem.0c00554
http://feeds.feedburner.com/~r/acs/bichaw/~4/CVBS2o_PcdY
More...
nmrlearner
Journal club
0
12-05-2020 07:44 AM
Researchers discover potential mechanism to combat haemorrhagic diseases - News-Medical.net
http://www.bionmr.com//t3.gstatic.com/images?q=tbn:ANd9GcTyM1uXTIaIw5q1INc3zkifPECmN3ZbTF8KFbDsA_fbY3BMFAuOMi8jvzcjz3gft3z24W0TdB4a
News-Medical.net
<img alt="" height="1" width="1">
Researchers discover potential mechanism to combat haemorrhagic diseases
News-Medical.net
"Our group used Nuclear Magnetic Resonance (NMR) spectroscopy studies to investigate the structural properties of an important viral protein required for virulence of the Rift Valley fever virus, a virus that causes infections in both humans and ...
and more »
Researchers discover potential mechanism to...
nmrlearner
Online News
0
05-11-2015 08:17 AM
Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation.
Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation.
Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation.
J Mol Biol. 2011 Aug 4;
Authors: Biljan I, Ilc G, Giachin G, Raspadori A, Zhukov I, Plavec J, Legname G
The development of transmissible spongiform encephalopathies (TSEs) is associated with the conversion of the cellular prion protein (PrP(C)) into a misfolded, pathogenic isoform (PrP(Sc)). Spontaneous generation...
nmrlearner
Journal club
0
08-16-2011 01:19 PM
Arginine interactions with anatase TiO(2) (100) surface and the perturbation of (49)T
Arginine interactions with anatase TiO(2) (100) surface and the perturbation of (49)Ti NMR chemical shifts - a DFT investigation: relevance to Renu-Seeram bio solar cell.
Related Articles Arginine interactions with anatase TiO(2) (100) surface and the perturbation of (49)Ti NMR chemical shifts - a DFT investigation: relevance to Renu-Seeram bio solar cell.
J Mol Model. 2010 Sep 21;
Authors: Koch R, Lipton AS, Filipek S, Renugopalakrishnan V
Density functional theoretical calculations have been utilized to investigate the interaction of the amino...