NMR Characterization of Information Flow and Allosteric Communities in the MAP Kinase p38?.
Sci Rep. 2016;6:28655
Authors: Aoto PC, Martin BT, Wright PE
Abstract
The intramolecular network structure of a protein provides valuable insights into allosteric sites and communication pathways. However, a straightforward method to comprehensively map and characterize these pathways is not currently available. Here we present an approach to characterize intramolecular network structure using NMR chemical shift perturbations. We apply the method to the mitogen activated protein kinase (MAPK) p38?. p38? contains allosteric sites that are conserved among eukaryotic kinases as well as unique to the MAPK family. How these regulatory sites communicate with catalytic residues is not well understood. Using our method, we observe and characterize for the first time information flux between regulatory sites through a conserved kinase infrastructure. This network is accessed, reinforced, and broken in various states of p38?, reflecting the functional state of the protein. We demonstrate that the approach detects critical junctions in the network corresponding to biologically significant allosteric sites and pathways.
NMR Structural/Functional Characterization of an Oncogenic Mutant of cAMP-Dependent Protein Kinase A: PRKACA-DNAJB1
NMR Structural/Functional Characterization of an Oncogenic Mutant of cAMP-Dependent Protein Kinase A: PRKACA-DNAJB1
Publication date: 16 February 2016
Source:Biophysical Journal, Volume 110, Issue 3, Supplement 1</br>
Author(s): Adak N. Karamafrooz, Jonggul Kim, Geoffrey Li, Sanford M. Simon, Susan S. Taylor, Gianluigi Veglia</br>
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Implementation and characterization of flow injection in dissolution dynamic nuclear polarization NMR spectroscopy
From The DNP-NMR Blog:
Implementation and characterization of flow injection in dissolution dynamic nuclear polarization NMR spectroscopy
Chen, H.Y. and C. Hilty, Implementation and characterization of flow injection in dissolution dynamic nuclear polarization NMR spectroscopy. ChemPhysChem, 2015. 16(12): p. 2646-52.
http://www.ncbi.nlm.nih.gov/pubmed/26139513
[NMR paper] Information content of long-range NMR data for the characterization of conformational heterogeneity.
Information content of long-range NMR data for the characterization of conformational heterogeneity.
Related Articles Information content of long-range NMR data for the characterization of conformational heterogeneity.
J Biomol NMR. 2015 Jun 5;
Authors: Andra?oj? W, Berlin K, Fushman D, Luchinat C, Parigi G, Ravera E, Sgheri L
Abstract
Long-range NMR data, namely residual dipolar couplings (RDCs) from external alignment and paramagnetic data, are becoming increasingly popular for the characterization of conformational...
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Information content of long-range NMR data for the characterization of conformational heterogeneity
Information content of long-range NMR data for the characterization of conformational heterogeneity
Abstract
Long-range NMR data, namely residual dipolar couplings (RDCs) from external alignment and paramagnetic data, are becoming increasingly popular for the characterization of conformational heterogeneity of multidomain biomacromolecules and protein complexes. The question addressed here is how much information is contained in these averaged data. We have analyzed and compared the information content of conformationally averaged RDCs caused by...
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06-05-2015 01:10 AM
[NMR paper] NMR spectroscopic characterization of new nonsymmetrical bispyridinium choline kinase inhibitors.
NMR spectroscopic characterization of new nonsymmetrical bispyridinium choline kinase inhibitors.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--media.wiley.com-assets-2250-98-WileyOnlineLibrary_FullTextOnline_120x27.gif Related Articles NMR spectroscopic characterization of new nonsymmetrical bispyridinium choline kinase inhibitors.
Magn Reson Chem. 2014 Aug;52(8):470-3
Authors: Rubio-Ruiz B, Espinosa A, Entrena Guadix A, Conejo-García A
PMID: 24916016
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[NMR paper] NMR reveals the allosteric opening and closing of Abelson tyrosine kinase by ATP-site and myristoyl pocket inhibitors.
NMR reveals the allosteric opening and closing of Abelson tyrosine kinase by ATP-site and myristoyl pocket inhibitors.
Related Articles NMR reveals the allosteric opening and closing of Abelson tyrosine kinase by ATP-site and myristoyl pocket inhibitors.
Proc Natl Acad Sci U S A. 2013 Nov 4;
Authors: Skora L, Mestan J, Fabbro D, Jahnke W, Grzesiek S
Abstract
Successful treatment of chronic myelogenous leukemia is based on inhibitors binding to the ATP site of the deregulated breakpoint cluster region (Bcr)-Abelson tyrosine kinase (Abl)...
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[NMR paper] Strategies for the NMR-based identification and optimization of allosteric protein kinase inhibitors.
Strategies for the NMR-based identification and optimization of allosteric protein kinase inhibitors.
Related Articles Strategies for the NMR-based identification and optimization of allosteric protein kinase inhibitors.
Chembiochem. 2005 Sep;6(9):1607-10
Authors: Jahnke W, Blommers MJ, Fernández C, Zwingelstein C, Amstutz R