Zooming in on protons: Neutron structure of protein kinase A trapped in a product complex - Science Advances
Zooming in on protons: Neutron structure of protein kinase A trapped in a product complex - Science Advances
Zooming in on protons: Neutron structure of protein kinase A trapped in a product complex Science AdvancesThe question vis-à-vis the chemistry of phosphoryl group transfer catalyzed by protein kinases remains a major challenge. The neutron diffraction structure of the ...
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04-12-2019 05:25 PM
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli - Science Advances
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli - Science Advances
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli Science AdvancesWith the increasing resistance of many Gram-negative bacteria to existing classes of antibiotics, identifying new paradigms in antimicrobial discovery is an ...
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04-12-2019 05:25 PM
Zooming in on protons: Neutron structure of protein kinase A trapped in a product complex - Science Advances
Zooming in on protons: Neutron structure of protein kinase A trapped in a product complex - Science Advances
Zooming in on protons: Neutron structure of protein kinase A trapped in a product complex Science AdvancesThe question vis-à-vis the chemistry of phosphoryl group transfer catalyzed by protein kinases remains a major challenge. The neutron diffraction structure of the ...
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03-24-2019 10:41 PM
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli - Science Advances
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli - Science Advances
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli Science AdvancesWith the increasing resistance of many Gram-negative bacteria to existing classes of antibiotics, identifying new paradigms in antimicrobial discovery is an ...
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01-07-2019 05:49 AM
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli - Science Advances
Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli - Science Advances
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Thanatin targets the intermembrane protein complex required for lipopolysaccharide transport in Escherichia coli
Science Advances
The NMR structure of LptA complexed with thanatin, reported here, superimposed upon the crystal structure of the LptA head-to-tail oligomer (PDB 2R1A), reveals that the thanatin binding site overlaps and would therefore block the interaction between ...
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11-25-2018 06:02 AM
[NMR paper] Solution NMR structure of the 48-kDa IIAMannose-HPr complex of the Escherichia coli m
Solution NMR structure of the 48-kDa IIAMannose-HPr complex of the Escherichia coli mannose phosphotransferase system.
Related Articles Solution NMR structure of the 48-kDa IIAMannose-HPr complex of the Escherichia coli mannose phosphotransferase system.
J Biol Chem. 2005 May 27;280(21):20775-84
Authors: Williams DC, Cai M, Suh JY, Peterkofsky A, Clore GM
The solution structure of the 48-kDa IIA(Man)-HPr complex of the mannose branch of the Escherichia coli phosphotransferase system has been solved by NMR using conjoined rigid body/torsion...
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11-24-2010 11:14 PM
[NMR paper] NMR studies of the Escherichia coli Trp repressor.trpRs operator complex.
NMR studies of the Escherichia coli Trp repressor.trpRs operator complex.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www3.interscience.wiley.com-aboutus-images-wiley_interscience_pubmed_logo_FREE_120x27.gif Related Articles NMR studies of the Escherichia coli Trp repressor.trpRs operator complex.
Eur J Biochem. 1996 Dec 15;242(3):567-75
Authors: Evans PD, Jaseja M, Jeeves M, Hyde EI
To understand the specificity of the Escherichia coli Trp repressor for its operators, we have begun to study complexes of the protein with...
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08-22-2010 02:20 PM
[NMR paper] NMR structure of Escherichia coli glutaredoxin 3-glutathione mixed disulfide complex:
NMR structure of Escherichia coli glutaredoxin 3-glutathione mixed disulfide complex: implications for the enzymatic mechanism.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles NMR structure of Escherichia coli glutaredoxin 3-glutathione mixed disulfide complex: implications for the enzymatic mechanism.
J Mol Biol. 1999 Feb 19;286(2):541-52
Authors: Nordstrand K, slund F, Holmgren A, Otting G, Berndt KD
Glutaredoxins (Grxs) catalyze reversible oxidation/reduction of...