QSY® 35 iodoacetamide - Citations

QSY® 35 iodoacetamide - Citations

View additional product information for QSY® 35 iodoacetamide - Citations (Q20348)

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Citations & References
Abstract
Spatial relationship between heads of dimeric Ncd in the presence of nucleotides and microtubules.
AuthorsHajdo L, Skowronek K, Kasprzak AA
JournalArch Biochem Biophys
PubMed ID14984201
'Kinesins are molecular motors that produce mechanical work at the expense of ATP hydrolysis. Here, we studied Ncd (non-claret disjunctional), a (-)-end-directed member of this superfamily. To gain insight into the mechanism by which Ncd generates force and movement, we measured distances between the heads in dimeric Ncd-250-700 using fluorescence ... More
Conformation coupled enzyme catalysis: single-molecule and transient kinetics investigation of dihydrofolate reductase.
AuthorsAntikainen NM, Smiley RD, Benkovic SJ, Hammes GG
JournalBiochemistry
PubMed ID16363797
'Ensemble kinetics and single-molecule fluorescence microscopy were used to study conformational transitions associated with enzyme catalysis by dihydrofolate reductase (DHFR). The active site loop of DHFR was labeled with a fluorescence quencher, QSY35, at amino acid position 17, and the fluorescent probe, Alexa555, at amino acid 37, by introducing cysteines ... More
Anthrax lethal factor inhibition.
AuthorsShoop WL, Xiong Y, Wiltsie J, Woods A, Guo J, Pivnichny JV, Felcetto T, Michael BF, Bansal A, Cummings RT, Cunningham BR, Friedlander AM, Douglas CM, Patel SB, Wisniewski D, Scapin G, Salowe SP, Zaller DM, Chapman KT, Scolnick EM, Schmatz DM, Bartizal K, MacCoss M, Hermes JD,
JournalProc Natl Acad Sci U S A
PubMed ID15911756
The primary virulence factor of Bacillus anthracis is a secreted zinc-dependent metalloprotease toxin known as lethal factor (LF) that is lethal to the host through disruption of signaling pathways, cell destruction, and circulatory shock. Inhibition of this proteolytic-based LF toxemia could be expected to provide therapeutic value in combination with ... More