[ASAP] Structure and Functionality of an Alkylated LixSiyOz Interphase for High-Energy Cathodes from DNP-ssNMR Spectroscopy
Structure and Functionality of an Alkylated LixSiyOz Interphase for High-Energy Cathodes from DNP-ssNMR Spectroscopy
Shira Haber, Rosy, Arka Saha, Olga Brontvein, Raanan Carmieli, Arava Zohar, Malachi Noked, and Michal Leskes
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.1c00215/20210322/images/medium/ja1c00215_0010.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.1c00215
http://feeds.feedburner.com/~r/acs/jacsat/~4/0X313-ywRB8
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03-23-2021 07:56 PM
[ASAP] Substrate Activation of the Low-Molecular Weight Protein Tyrosine Phosphatase from Mycobacterium tuberculosis
Substrate Activation of the Low-Molecular Weight Protein Tyrosine Phosphatase from Mycobacterium tuberculosis
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.0c00059/20200312/images/medium/bi0c00059_0009.gif
Biochemistry
DOI: 10.1021/acs.biochem.0c00059
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03-16-2020 04:59 PM
Characterization of Protein Tyrosine Phosphatase 1BInhibition by Chlorogenic Acid and Cichoric Acid
Characterization of Protein Tyrosine Phosphatase 1BInhibition by Chlorogenic Acid and Cichoric Acid
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.6b01025/20161227/images/medium/bi-2016-01025j_0008.gif
Biochemistry
DOI: 10.1021/acs.biochem.6b01025
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/bichaw/~4/pzC-PLk80yY
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12-27-2016 11:04 PM
Trichoketides A and B, two new protein tyrosine phosphatase 1B inhibitors from ... - Nature.com
Trichoketides A and B, two new protein tyrosine phosphatase 1B inhibitors from ... - Nature.com
<img alt="" height="1" width="1">
Trichoketides A and B, two new protein tyrosine phosphatase 1B inhibitors from ...
Nature.com
The 1H and 13C NMR spectra (in acetone-d6) showed 23 proton and 16 carbon signals (Table 1) that were classified into one methyl, eight sp3 methylene, two sp3 oxygenated methine, two sp2 methine, two sp2 quaternary and one carbonyl carbons through ...
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04-22-2015 03:33 PM
A 1H NMR metabolic profiling to the assessment of protein tyrosine phosphatase 1B role in liver regeneration after partial hepatectomy
A 1H NMR metabolic profiling to the assessment of protein tyrosine phosphatase 1B role in liver regeneration after partial hepatectomy
Available online 12 December 2012
Publication year: 2012
Source:Biochimie</br>
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Protein tyrosine phosphatase 1B (PTP1B) is a negative regulator of the tyrosine kinase growth factor signaling pathway, which is involved in major physiological mechanisms such as liver regeneration. We investigate early hepatic metabolic events produced by partial hepatectomy (PHx) for PTP1B deficient (PTP1B KO) and wild type (WT) mice using proton...
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02-03-2013 10:13 AM
Design and NMR Studies of Cyclic Peptides Targeting the N-Terminal Domain of the Protein Tyrosine Phosphatase YopH.
Design and NMR Studies of Cyclic Peptides Targeting the N-Terminal Domain of the Protein Tyrosine Phosphatase YopH.
Design and NMR Studies of Cyclic Peptides Targeting the N-Terminal Domain of the Protein Tyrosine Phosphatase YopH.
Chem Biol Drug Des. 2010 Nov 30;
Authors: Leone M, Barile E, Dahl R, Pellecchia M
We report on the design and evaluation of novel cyclic peptides targeting the N-terminal domain of the protein tyrosine phosphatase YopH from Yersinia. Cyclic peptides have been designed based on a short sequence from the protein SKAP-HOM...
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12-02-2010 02:54 PM
[NMR paper] NMR assignments of a low molecular weight protein tyrosine phosphatase (PTPase) from
NMR assignments of a low molecular weight protein tyrosine phosphatase (PTPase) from Bacillus subtilis.
Related Articles NMR assignments of a low molecular weight protein tyrosine phosphatase (PTPase) from Bacillus subtilis.
J Biomol NMR. 2005 Apr;31(4):363
Authors: Xu H, Zhang P, Jin C
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[NMR paper] Intramolecular dynamics of low molecular weight protein tyrosine phosphatase in monom
Intramolecular dynamics of low molecular weight protein tyrosine phosphatase in monomer-dimer equilibrium studied by NMR: a model for changes in dynamics upon target binding.
Related Articles Intramolecular dynamics of low molecular weight protein tyrosine phosphatase in monomer-dimer equilibrium studied by NMR: a model for changes in dynamics upon target binding.
J Mol Biol. 2002 Sep 6;322(1):137-52
Authors: Akerud T, Thulin E, Van Etten RL, Akke M
Low molecular weight protein tyrosine phosphatase (LMW-PTP) dimerizes in the phosphate-bound...