[ASAP] Can Protein Expression Be Regulated by Modulation of tRNA Modification Profiles?
Can Protein Expression Be Regulated by Modulation of tRNA Modification Profiles?
https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.8b01035/20181218/images/medium/bi-2018-01035u_0003.gif
Biochemistry
DOI: 10.1021/acs.biochem.8b01035
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nmrlearner
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01-07-2019 05:49 AM
[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
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nmrlearner
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06-11-2018 07:38 PM
[NMR paper] Rational tuning of fluorobenzene probes for cysteine-selective protein modification
Rational tuning of fluorobenzene probes for cysteine-selective protein modification
Fluorobenzene probes for protein profiling through selective cysteine labeling have been developed by rational reactivity tuning. Tuning was achieved by selecting an electron-withdrawing para-substituent combined with variation of the number of fluorine substituents. Optimized probes chemo-selectively arylated cysteine residues in proteins under aqueous conditions. Probes linked to azide, biotin or a fluorophore were applicable to labeling of eGFP and albumin. Selective inhibition of cysteine proteases...
nmrlearner
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02-22-2018 02:48 PM
Selective Modulation of Protein Kinase C ? overProtein Kinase C ? by Curcumin and Its Derivatives in CHO-K1Cells
Selective Modulation of Protein Kinase C ? overProtein Kinase C ? by Curcumin and Its Derivatives in CHO-K1Cells
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.6b00057/20160325/images/medium/bi-2016-000572_0010.gif
Biochemistry
DOI: 10.1021/acs.biochem.6b00057
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nmrlearner
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03-26-2016 12:14 PM
[NMR paper] Rearrangement of charge-charge interactions in variant ubiquitins as detected by doub
Rearrangement of charge-charge interactions in variant ubiquitins as detected by double-mutant cycles and NMR.
Related Articles Rearrangement of charge-charge interactions in variant ubiquitins as detected by double-mutant cycles and NMR.
J Mol Biol. 2003 Sep 26;332(4):927-36
Authors: Sundd M, Robertson AD
Previous studies of ubiquitin disclosed numerous charge-charge interactions on the protein's surface. To investigate how neighboring residues influence the strength of these interactions, double-mutant cycles are combined with pK(a)...
nmrlearner
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11-24-2010 09:16 PM
[NMR paper] Oxygen as a paramagnetic probe of membrane protein structure by cysteine mutagenesis
Oxygen as a paramagnetic probe of membrane protein structure by cysteine mutagenesis and (19)F NMR spectroscopy.
Related Articles Oxygen as a paramagnetic probe of membrane protein structure by cysteine mutagenesis and (19)F NMR spectroscopy.
J Am Chem Soc. 2002 Feb 27;124(8):1778-81
Authors: Luchette PA, Prosser RS, Sanders CR
Oxygen solubility increases toward the hydrophobic interior of membranes. Using NMR, this O(2) solubility gradient gives rise to an exquisite range of position-dependent paramagnetic effects at partial pressures of 100...
nmrlearner
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11-24-2010 08:49 PM
[NMR paper] Mutational analysis and NMR spectroscopy of quail cysteine and glycine-rich protein C
Mutational analysis and NMR spectroscopy of quail cysteine and glycine-rich protein CRP2 reveal an intrinsic segmental flexibility of LIM domains.
Related Articles Mutational analysis and NMR spectroscopy of quail cysteine and glycine-rich protein CRP2 reveal an intrinsic segmental flexibility of LIM domains.
J Mol Biol. 1999 Oct 1;292(4):893-908
Authors: Kloiber K, Weiskirchen R, Kräutler B, Bister K, Konrat R
The LIM domain is a conserved cysteine and histidine-containing structural module of two tandemly arranged zinc fingers. It has been...
nmrlearner
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11-18-2010 08:31 PM
[NMR paper] Orientation and mobility of the heme vinyl groups in myoglobins with the aid of NOE a
Orientation and mobility of the heme vinyl groups in myoglobins with the aid of NOE and MATDUHM NMR.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles Orientation and mobility of the heme vinyl groups in myoglobins with the aid of NOE and MATDUHM NMR.
Biochim Biophys Acta. 1992 Apr 8;1120(2):173-82
Authors: Yamamoto Y, Iwafune K, Nanai N, Chûjô R, Inoue Y, Suzuki T
The heme vinyl substituents in a shark (Galeorhinus japonicus) myoglobin in its met-cyano form (MbCN)...