Andrea Bertarello, Ladislav Benda, Kevin J. Sanders, Andrew J. Pell, Michael J. Knight, Vladimir Pelmenschikov, Leonardo Gonnelli, Isabella C. Felli, Martin Kaupp, Lyndon Emsley, Roberta Pierattelli, and Guido Pintacuda
Journal of the American Chemical Society
DOI: 10.1021/jacs.0c07339
[ASAP] Structure and Catalytic Characterization of a Second Framework Al(IV) Site in Zeolite Catalysts Revealed by NMR at 35.2 T
Structure and Catalytic Characterization of a Second Framework Al(IV) Site in Zeolite Catalysts Revealed by NMR at 35.2 T
Kuizhi Chen*†, Sarah Horstmeier‡, Vy. T. Nguyen?, Bin Wang?, Steven P. Crossley?, Tram Pham?, Zhehong Gan†, Ivan Hung†, and Jeffery L. White*§
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.0c00590/20200413/images/medium/ja0c00590_0007.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.0c00590
http://feeds.feedburner.com/~r/acs/jacsat/~4/t3FuVeVyDZo
nmrlearner
Journal club
0
04-20-2020 05:10 PM
[ASAP] Skp1 Dimerization Conceals Its F-Box Protein Binding Site
Skp1 Dimerization Conceals Its F-Box Protein Binding Site
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.0c00094/20200413/images/medium/bi0c00094_0005.gif
Biochemistry
DOI: 10.1021/acs.biochem.0c00094
http://feeds.feedburner.com/~r/acs/bichaw/~4/e-R9Z1H_9Zs
More...
nmrlearner
Journal club
0
04-20-2020 05:10 PM
[ASAP] Cyanylated Cysteine Reports Site-Specific Changes at Protein–Protein-Binding Interfaces Without Perturbation
Cyanylated Cysteine Reports Site-Specific Changes at Protein–Protein-Binding Interfaces Without Perturbation
https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.8b00283/20180605/images/medium/bi-2018-00283c_0004.gif
Biochemistry
DOI: 10.1021/acs.biochem.8b00283
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/bichaw/~4/gdWE1PdRzx4
More...
nmrlearner
Journal club
0
06-11-2018 07:38 PM
[NMR paper] Long-range paramagnetic NMR data can provide a closer look on metal coordination in metalloproteins.
Long-range paramagnetic NMR data can provide a closer look on metal coordination in metalloproteins.
Related Articles Long-range paramagnetic NMR data can provide a closer look on metal coordination in metalloproteins.
J Biol Inorg Chem. 2017 Dec 07;:
Authors: Cerofolini L, Staderini T, Giuntini S, Ravera E, Fragai M, Parigi G, Pierattelli R, Luchinat C
Abstract
Paramagnetic NMR data can be profitably incorporated in structural refinement protocols of metalloproteins or metal-substituted proteins, mostly as distance or angle...
nmrlearner
Journal club
0
12-10-2017 01:21 AM
Heavy metal binding domain in a cysteine-rich protein may be sea snail adaptation to metal stress - Phys.Org
Heavy metal binding domain in a cysteine-rich protein may be sea snail adaptation to metal stress - Phys.Org
<img alt="" height="1" width="1">
Heavy metal binding domain in a cysteine-rich protein may be sea snail adaptation to metal stress
Phys.Org
Structural Adaptation of a Protein to Increased Metal Stress: NMR Structure of a Marine Snail Metallothionein with an Additional Domain. Credit: Wiley. A special type of small sulfur-rich protein, metallothioneins, have an extraordinary capability for ...
Read here
nmrlearner
Online News
0
03-24-2017 10:00 AM
[NMR paper] Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR.
Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR.
Related Articles Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR.
J Vis Exp. 2013;(82)
Authors: Shoshan MS, Tshuva EY, Shalev DE
Abstract
Copper (I) binding by metallochaperone transport proteins prevents copper oxidation and release of the toxic ions that may participate in harmful redox reactions. The Cu (I) complex of the peptide model of a Cu (I) binding metallochaperone protein, which includes the...
nmrlearner
Journal club
0
01-01-2014 03:05 PM
[NMR paper] The Involvement of Amino Acid Side Chains in Shielding the Nickel Coordination Site: An NMR Study.
The Involvement of Amino Acid Side Chains in Shielding the Nickel Coordination Site: An NMR Study.
The Involvement of Amino Acid Side Chains in Shielding the Nickel Coordination Site: An NMR Study.
Molecules. 2013;18(10):12396-12414
Authors: Medici S, Peana M, Nurchi VM, Zoroddu MA
Abstract
Coordination of proteins and peptides to metal ions is known to affect their properties, often by a change in their structural organization. Side chains of the residues directly involved in metal binding or very close to the coordination centre...
nmrlearner
Journal club
0
10-11-2013 10:43 AM
[NMR paper] NMR evidence for perturbation of the copper coordination sphere upon chemical modific
NMR evidence for perturbation of the copper coordination sphere upon chemical modification of arginine 141 in bovine Cu,Zn superoxide dismutase.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles NMR evidence for perturbation of the copper coordination sphere upon chemical modification of arginine 141 in bovine Cu,Zn superoxide dismutase.
Arch Biochem Biophys. 1991 Apr;286(1):222-5
Authors: Paci M, Desideri A, Sette M, Rotilio G
The reaction of the Cu,Co derivative of...