The FEBS journal · 2015
Crystal structures of apo-DszC and FMN-bound DszC from Rhodococcus erythropolis D-1.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Guan Li-Jun, Lee Woo Cheol, Wang Shipeng, Ohshiro Takashi, Izumi Yoshikazu, Ohtsuka Jun, Tanokura Masaru
Аннотация
UNLABELLED: The release of SO2 from petroleum products derived from crude oil, which contains sulfur compounds such as dibenzothiophene (DBT), leads to air pollution. The '4S' metabolic pathway catalyzes the sequential conversion of DBT to 2-hydroxybiphenyl via three enzymes encoded by the dsz operon in several bacterial species. DszC (DBT monooxygenase), from Rhodococcus erythropolis D-1 is involved in the first two steps of the '4S' pathway. Here, we determined the first crystal structure of FMN-bound DszC, and found that two distinct conformations occur in the loop region (residues 131-142) adjacent to the active site. On the basis of the DszC-FMN structure and the previously reported apo structures of DszC homologs, the binding site for DBT and DBT sulfoxide is proposed.
DATABASE: The atomic coordinates and structure factors for apo-DszC (PDB code: 3X0X) and DszC-FMN (PDB code: 3X0Y) have been deposited in the Protein Data Bank (http://www.rcsb.org).
DATABASE: The atomic coordinates and structure factors for apo-DszC (PDB code: 3X0X) and DszC-FMN (PDB code: 3X0Y) have been deposited in the Protein Data Bank (http://www.rcsb.org).
Предметные рубрики MeSH
Air PollutantsApoenzymesBacterial ProteinsBiodegradation, EnvironmentalCatalytic DomainCrystallography, X-RayFlavin MononucleotideGenes, BacterialMetabolic Networks and PathwaysModels, MolecularOxidoreductasesPetroleumProtein ConformationRhodococcusStatic ElectricitySubstrate SpecificitySulfur DioxideThiophenes