Molecular Recognition of Long Dicarboxylate/Dicarboxylic Species via Supramolecular/Coordinative Interactions with Ditopic Receptors. Crystal Structure of {[Cu2L(H2O)2]⊃Pimelate}(ClO4)2

1999 ◽  
Vol 38 (4) ◽  
pp. 620-621 ◽  
Author(s):  
Carla Bazzicalupi ◽  
Andrea Bencini ◽  
Antonio Bianchi ◽  
Vieri Fusi ◽  
Enrique Garcia-España ◽  
...  
2018 ◽  
Vol 74 (7) ◽  
pp. 690-694 ◽  
Author(s):  
Ian W. Windsor ◽  
Ronald T. Raines

Crystal structures of inactive variants of HIV-1 protease bound to peptides have revealed how the enzyme recognizes its endogenous substrates. The best of the known substrates is, however, a nonnatural substrate that was identified by directed evolution. The crystal structure of the complex between this substrate and the D25N variant of the protease is reported at a resolution of 1.1 Å. The structure has several unprecedented features, especially the formation of additional hydrogen bonds between the enzyme and the substrate. This work expands the understanding of molecular recognition by HIV-1 protease and informs the design of new substrates and inhibitors.


2013 ◽  
Vol 1038 ◽  
pp. 188-193 ◽  
Author(s):  
Ikuhide Fujisawa ◽  
Yuji Kitamura ◽  
Rumi Okamoto ◽  
Kazutaka Murayama ◽  
Ryo Kato ◽  
...  

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