Crystal structures of FolM alternative dihydrofolate reductase 1 from Brucella suis and Brucella canis

Author:

Porter Imani,Neal TrinityORCID,Walker ZionORCID,Hayes Dylan,Fowler Kayla,Billups Nyah,Rhoades Anais,Smith Christian,Smith Kaelyn,Staker Bart L.,Dranow David M.,Mayclin Stephen J.,Subramanian Sandhya,Edwards Thomas E.ORCID,Myler Peter J.,Asojo Oluwatoyin A.ORCID

Abstract

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.

Funder

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

Publisher

International Union of Crystallography (IUCr)

Subject

Condensed Matter Physics,Genetics,Biochemistry,Structural Biology,Biophysics

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Using protein crystallography to engage HBCU students in biochemistry;Acta Crystallographica Section A Foundations and Advances;2022-07-29

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