Metal Ion Substitution in the Catalytic Site Greatly Affects the Binding of Sulfhydryl-Containing Compounds to Leucyl Aminopeptidase†,‡

Biochemistry ◽  
2006 ◽  
Vol 45 (10) ◽  
pp. 3226-3234 ◽  
Author(s):  
Mario Cappiello ◽  
Vincenzo Alterio ◽  
Pietro Amodeo ◽  
Antonella Del Corso ◽  
Andrea Scaloni ◽  
...  
The Analyst ◽  
2010 ◽  
Vol 135 (1) ◽  
pp. 140-148 ◽  
Author(s):  
Wei Zhang ◽  
Jian-Feng Chen ◽  
Liu-Yin Fan ◽  
Cheng-Xi Cao ◽  
Ji-Cun Ren ◽  
...  

2012 ◽  
Vol 48 (47) ◽  
pp. 5826 ◽  
Author(s):  
David A. Leigh ◽  
Paul J. Lusby ◽  
Alexandra M. Z. Slawin ◽  
D. Barney Walker

1988 ◽  
Vol 110 (20) ◽  
pp. 6716-6720 ◽  
Author(s):  
Ruth. Jones ◽  
Peter P. Edwards ◽  
Martin R. Harrison ◽  
Thitinant. Thanyasiri ◽  
Ekkehard. Sinn

1988 ◽  
Vol 41 (6) ◽  
pp. 957 ◽  
Author(s):  
NF Curtis

Reaction of nickel(II) with 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene diperchlorate in the presence of ammonia yields a lilac- coloured complex of nickel(II) with 13-imino-4,4,6,11,11-pentamethyl-3,7,10-triazatetradec-6-en-1-amine, a pentadentate ligand with one primary and two secondary amino, plus one primary and one secondary imino , donor groups. The copper(II) complex of the ligand was formed from the nickel(II) compound by metal-ion substitution. The cations have d-d spectra indicative of five-coordination. The complex cations undergo a reversible protonation reaction with a change from five-coordinate to square planar, with a colour change for nickel(II) from lilac (triplet ground state) to yellow (singlet ground state), and for copper(II) from blue to violet. The compounds of the homologous ligand 4,6,11-triethyl-13-imino-4,11- dimethyl-3,7,10-triazapentadec-6-en-1-amine were similarly prepared, and have similar properties.


2008 ◽  
Vol 47 (23) ◽  
pp. 9240-9247 ◽  
Author(s):  
Sounak Roy ◽  
A. Marimuthu ◽  
Parag A. Deshpande ◽  
M. S. Hegde ◽  
Giridhar Madras

1995 ◽  
Vol 199 (4) ◽  
pp. 317-324
Author(s):  
Ecaterina Princz ◽  
Ana Nimara ◽  
Livia Martony
Keyword(s):  

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