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Prokaryotic genes related to the oxygenase domain of mammalian nitric oxide synthases (NOSs) have recently been identified. Although they catalyze the same reaction as the eukaryotic NOS oxygenase domain, their biological function(s) are unknown. In order to explore rationally the biochemistry and evolution of the prokaryotic NOS family, we have determined the crystal structure of SANOS, from methicillin-resistant Staphylococcus aureus (MRSA), to 2.4 A. Haem and S-ethylisothiourea (SEITU) are bound at the SANOS active site, while the intersubunit site, occupied by the redox cofactor tetrahydrobiopterin (H(4)B) in mammalian NOSs, has NAD(+) bound in SANOS. In common with all bacterial NOSs, SANOS lacks the N-terminal extension responsible for stable dimerization in mammalian isoforms, but has alternative interactions to promote dimer formation.

Type

Journal article

Journal

Structure

Publication Date

12/2002

Volume

10

Pages

1687 - 1696

Keywords

Amino Acid Sequence, Animals, Base Sequence, Binding Sites, Catalysis, Cattle, Crystallography, X-Ray, DNA Primers, Dimerization, Heme, Mice, Molecular Sequence Data, Nitric Oxide Synthase, Protein Conformation, Sequence Homology, Amino Acid, Staphylococcus aureus