Probing the Role of the Heme Distal and Proximal Environmentin Ligand Dynamics in the Signal Transducer Protein HemAT by Time-ResolvedStep-Scan FTIR and Resonance Raman Spectroscopy
Probing the Role of the Heme Distal and Proximal Environmentin Ligand Dynamics in the Signal Transducer Protein HemAT by Time-ResolvedStep-Scan FTIR and Resonance Raman Spectroscopy
Posttranslational Modification of Heme b in a Bacterial Peroxidase: The Role of Heme to Protein Ester Bondsin Ligand Binding and Catalysis
Posttranslational Modification of Heme b in a Bacterial Peroxidase: The Role of Heme to Protein Ester Bondsin Ligand Binding and Catalysis
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.7b00632/20170815/images/medium/bi-2017-00632n_0009.gif
Biochemistry
DOI: 10.1021/acs.biochem.7b00632
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/bichaw/~4/HAn5BdAvWAg
More...
nmrlearner
Journal club
0
08-17-2017 12:56 AM
Dynamics of Lysine as a Heme Axial Ligand: NMR Analysisof the Chlamydomonas reinhardtii Hemoglobin THB1
Dynamics of Lysine as a Heme Axial Ligand: NMR Analysisof the Chlamydomonas reinhardtii Hemoglobin THB1
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.6b00926/20170118/images/medium/bi-2016-00926m_0015.gif
Biochemistry
DOI: 10.1021/acs.biochem.6b00926
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/bichaw/~4/Aypv4xjT108
More...
nmrlearner
Journal club
0
01-19-2017 08:56 AM
[NMR paper] Probing Conformational Exchange Dynamics in a Short-Lived Protein Folding Intermediate by Real-Time Relaxation-Dispersion NMR.
Probing Conformational Exchange Dynamics in a Short-Lived Protein Folding Intermediate by Real-Time Relaxation-Dispersion NMR.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-pubmed-acspubs.jpg Related Articles Probing Conformational Exchange Dynamics in a Short-Lived Protein Folding Intermediate by Real-Time Relaxation-Dispersion NMR.
J Am Chem Soc. 2017 Jan 11;:
Authors: Franco R, Gil-Caballero S, Ayala I, Favier A, Brutscher B
Abstract
NMR spectroscopy is a powerful tool for studying...
nmrlearner
Journal club
0
01-12-2017 03:48 AM
[NMR paper] The dynamics of lysine as a heme axial ligand: NMR analysis of the Chlamydomonas reinhardtii hemoglobin THB1.
The dynamics of lysine as a heme axial ligand: NMR analysis of the Chlamydomonas reinhardtii hemoglobin THB1.
Related Articles The dynamics of lysine as a heme axial ligand: NMR analysis of the Chlamydomonas reinhardtii hemoglobin THB1.
Biochemistry. 2016 Dec 29;:
Authors: Preimesberger MR, Majumdar A, Lecomte JT
Abstract
Nitrate metabolism in Chlamydomonas reinhardtii involves THB1, a monomeric hemoglobin thought to function as a nitric oxide dioxygenase (NOD). NOD activity requires dioxygen and nitric oxide binding followed by...
[NMR paper] The role of water in protein's behavior: The two dynamical crossovers studied by NMR and FTIR techniques.
The role of water in protein's behavior: The two dynamical crossovers studied by NMR and FTIR techniques.
Related Articles The role of water in protein's behavior: The two dynamical crossovers studied by NMR and FTIR techniques.
Comput Struct Biotechnol J. 2015;13:33-7
Authors: Mallamace F, Corsaro C, Mallamace D, Vasi S, Vasi C, Dugo G
Abstract
nmrlearner
Journal club
0
03-10-2015 07:22 PM
[NMR paper] Enzyme Active Site Interactions by Raman/FTIR, NMR, and Ab Initio Calculations.
Enzyme Active Site Interactions by Raman/FTIR, NMR, and Ab Initio Calculations.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles Enzyme Active Site Interactions by Raman/FTIR, NMR, and Ab Initio Calculations.
Adv Protein Chem Struct Biol. 2013;93:153-82
Authors: Deng H
Abstract
Characterization of enzyme active site structure and interactions at high resolution is important for the understanding of the enzyme catalysis. Vibrational frequency and...
nmrlearner
Journal club
0
09-11-2013 09:15 PM
[NMR paper] 1H NMR study of the role of heme carboxylate side chains in modulating heme pocket st
1H NMR study of the role of heme carboxylate side chains in modulating heme pocket structure and the mechanism of reconstitution of cytochrome b5.
Related Articles 1H NMR study of the role of heme carboxylate side chains in modulating heme pocket structure and the mechanism of reconstitution of cytochrome b5.
Biochemistry. 1991 Feb 19;30(7):1878-87
Authors: Lee KB, La Mar GN, Pandey RK, Rezzano IN, Mansfield KE, Smith KM
1H nuclear magnetic resonance spectroscopy was used to assign the hyperfine-shifted resonances and determine the position of...