Department of Chemistry and Biochemistry, Hampton University, 100 William R. Harvey Way, Hampton, VA 23668, USA.
Seattle Structural Genomics Center for Infectious Disease (SSGCID), Seattle, Washington, USA.
Acta Crystallogr F Struct Biol Commun. 2022 Jan 1;78(Pt 1):31-38. doi: 10.1107/S2053230X21013078.
Members of the bacterial genus Brucella cause brucellosis, a zoonotic disease that affects both livestock and wildlife. Brucella are category B infectious agents that can be aerosolized for biological warfare. As part of the structural genomics studies at the Seattle Structural Genomics Center for Infectious Disease (SSGCID), FolM alternative dihydrofolate reductases 1 from Brucella suis and Brucella canis were produced and their structures are reported. The enzymes share ∼95% sequence identity but have less than 33% sequence identity to other homologues with known structure. The structures are prototypical NADPH-dependent short-chain reductases that share their highest tertiary-structural similarity with protozoan pteridine reductases, which are being investigated for rational therapeutic development.
布鲁氏菌属的细菌成员引起布鲁氏菌病,一种影响牲畜和野生动物的人畜共患病。布鲁氏菌是可气溶胶化用于生物战的 B 类传染性病原体。作为西雅图传染病结构基因组学中心(SSGCID)结构基因组学研究的一部分,从猪布鲁氏菌和犬布鲁氏菌中产生了 FolM 替代二氢叶酸还原酶 1,并报告了它们的结构。这些酶具有约 95%的序列同一性,但与其他具有已知结构的同源物的序列同一性小于 33%。这些结构是典型的 NADPH 依赖性短链还原酶,与正在进行合理治疗开发研究的原生动物蝶呤还原酶具有最高的三级结构相似性。