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Monomeric sarcosine oxidase: structure of a covalently flavinylated amine oxidizing enzyme
Journal article   Open access   Peer reviewed

Monomeric sarcosine oxidase: structure of a covalently flavinylated amine oxidizing enzyme

Peter Trickey, Mary Ann Wagner, Marilyn Schuman Jorns and F Scott Mathews
Structure (London), v 7(3), pp 331-345
1999
PMID: 10368302
url
https://doi.org/10.1016/S0969-2126(99)80043-4View
Published, Version of Record (VoR) Open

Abstract

X-ray crystallography flavoprotein oxidase covalent flavinylation amine oxidation enzyme mechanism
Background: Monomeric sarcosine oxidases (MSOXs) are among the simplest members of a recently recognized family of eukaryotic and prokaryotic enzymes that catalyze similar oxidative reactions with various secondary or tertiary amino acids and contain covalently bound flavins. Other members of this family include heterotetrameric sarcosine oxidase, N-methyltryptophan oxidase and pipecolate oxidase. Mammalian sarcosine dehydrogenase and dimethylglycine dehydrogenase may be more distantly related family members. Results: The X-ray crystal structure of MSOX from Bacillus sp. B-0618, expressed in Escherichia coli, has been solved at 2.0 Å resolution by multiwavelength anomalous dispersion (MAD) from crystals of the selenomethionine-substituted enzyme. Fourteen selenium sites, belonging to two MSOX molecules in the asymmetric unit, were used for MAD phasing and to define the local twofold symmetry axis for electron-density averaging. The structures of the native enzyme and of two enzyme–inhibitor complexes were also determined. Conclusions: MSOX is a two-domain protein with an overall topology most similar to that of D-amino acid oxidase, with which it shares 14% sequence identity. The flavin ring is located in a very basic environment, making contact with sidechains of arginine, lysine, histidine and the N-terminal end of a helix dipole. The flavin is covalently attached through an 8 α–S-cysteinyl linkage to Cys315 of the catalytic domain. Covalent attachment is probably self-catalyzed through interactions with the positive sidechains and the helix dipole. Substrate binding is probably stabilized by hydrogen bonds between the substrate carboxylate and two basic sidechains, Arg52 and Lys348, located above the re face of the flavin ring.

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Collaboration types
Domestic collaboration
Web of Science research areas
Biochemistry & Molecular Biology
Biophysics
Cell Biology
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