Insights into metal ion binding in phospholipases A2: ultra high-resolution crystal structures of an acidic phospholipase A2 in the Ca2+ free and bound states

Biochimie ◽  
2006 ◽  
Vol 88 (5) ◽  
pp. 543-549 ◽  
Author(s):  
M.T. Murakami ◽  
A. Gabdoulkhakov ◽  
N. Genov ◽  
A.C.O. Cintra ◽  
C. Betzel ◽  
...  
2003 ◽  
Vol 59 (11) ◽  
pp. o629-o633 ◽  
Author(s):  
Paul V. Bernhardt ◽  
Lorraine M. Caldwell ◽  
David B. Lovejoy ◽  
Des R. Richardson

The X-ray crystal structures are reported of four novel and potentially O,N,S-tridentate donor ligands that demonstrate antitumour activity. These ligands are 1-[(4-methylthiosemicarbazono)methyl]-2-naphthol, C13H13N3OS, (III), 1-[(4-ethylthiosemicarbazono)methyl]-2-naphthol, C14H15N3OS, (IV), 1-[(4-phenylthiosemicarbazono)methyl]-2-naphthol, C18H15N3OS, (V), and 1-[(4,4-dimethylthiosemicarbazono)methyl]-2-naphthol dimethyl sulfoxide solvate, C14H15N3OS·C2H6OS, (VI). These chelators are N4-substituted thiosemicarbazones, each based on the same parent aldehyde, namely 2-zhydroxynaphthalene-1-carboxaldehyde isonicotinoylhydrazone. Conformational variations within this series are discussed in relation to the optimum conformation for metal-ion binding.


1989 ◽  
Vol 122 (8) ◽  
pp. 1433-1438 ◽  
Author(s):  
Hubert Schmidbaur ◽  
Ina Bach ◽  
Dallas L. Wilkinson ◽  
Gerhard Müller

1989 ◽  
Vol 122 (8) ◽  
pp. 1439-1444 ◽  
Author(s):  
Hubert Schmidbaur ◽  
Ina Bach ◽  
Dallas L. Wilkinson ◽  
Gerhard Müller

2004 ◽  
Vol 69 (4) ◽  
pp. 885-896 ◽  
Author(s):  
Luisa Stella Dolci ◽  
Péter Huszthy ◽  
Erika Samu ◽  
Marco Montalti ◽  
Luca Prodi ◽  
...  

Enantiomerically pure dimethyl- and diisobutyl-substituted phenazino-18-crown-6 ligands bind metal and ammonium ions and also primary aralkylammonium perchlorates in acetonitrile with high affinity, causing pronounced changes in their luminescence properties. In addition, they show enantioselectivity towards chiral primary aralkylammonium perchlorates. The possibility to monitor the binding process by photoluminescence spectroscopy can gain ground for the design of very efficient enantioselective chemosensors for chiral species. The observed changes in the photophysical properties are also an important tool for understanding the interactions present in the adduct.


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