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. 2004 May 7;304(5672):867-70.
doi: 10.1126/science.1095109.

Side-on copper-nitrosyl coordination by nitrite reductase

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Side-on copper-nitrosyl coordination by nitrite reductase

Elitza I Tocheva et al. Science. .

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.

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Comment in

  • Biophysics. Catching copper in the act.
    Aboelella NW, Reynolds AM, Tolman WB. Aboelella NW, et al. Science. 2004 May 7;304(5672):836-7. doi: 10.1126/science.1098301. Science. 2004. PMID: 15131298 No abstract available.

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