Title of article :
Domain Swing Upon His to Ala Mutation in Nitrite Reductase of Pseudomonas aeruginosa
Author/Authors :
Kieron Brown، نويسنده , , Veronique Roig-Zamboni، نويسنده , , Francesca Cutruzzolà، نويسنده , , Marzia Arese، نويسنده , , Wenliang Sun، نويسنده , , Maurizio Brunori، نويسنده , , Dominique Bourgeois and Christian Cambillau، نويسنده , , Mariella Tegoni، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
14
From page :
541
To page :
554
Abstract :
The nitrite reductase (NIR) from Pseudomonas aeruginosa (NIR-Pa) is a soluble enzyme catalysing the reduction of nitrite (NO2−) to nitric oxide (NO). The enzyme is a 120 kDa homodimer, in which the monomers carry a c-heme domain and a d1-heme domain. The structures of the enzyme in both the oxidised and reduced state were solved previously and indicate His327 and His369 as putative catalytic residues. The kinetic characterisation of site-directed mutants has shown that the substitution of either one of these two His with Ala dramatically reduces the physiologically relevant reactivity towards nitrite, leaving the reactivity towards oxygen unaffected.
Keywords :
Pseudomonas aeruginosa , nitrite reductase , Heme , X-ray structure analysis , site-directed mutants
Journal title :
Journal of Molecular Biology
Serial Year :
2001
Journal title :
Journal of Molecular Biology
Record number :
1241090
Link To Document :
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