| Literature DB >> 15131305 |
Elitza I Tocheva1, Federico I Rosell, A Grant Mauk, Michael E P Murphy.
Abstract
A copper-nitrosyl intermediate forms during the catalytic cycle of nitrite reductase, the enzyme that mediates the committed step in bacterial denitrification. The crystal structure of a type 2 copper-nitrosyl complex of nitrite reductase reveals an unprecedented side-on binding mode in which the nitrogen and oxygen atoms are nearly equidistant from the copper cofactor. Comparison of this structure with a refined nitrite-bound crystal structure explains how coordination can change between copper-oxygen and copper-nitrogen during catalysis. The side-on copper-nitrosyl in nitrite reductase expands the possibilities for nitric oxide interactions in copper proteins such as superoxide dismutase and prions.Entities:
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Year: 2004 PMID: 15131305 DOI: 10.1126/science.1095109
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728