7ZZX
Crystal structure of Candida auris DHFR in apo form
Summary for 7ZZX
Entry DOI | 10.2210/pdb7zzx/pdb |
Descriptor | Dihydrofolate reductase (2 entities in total) |
Functional Keywords | dihydrofolate reductase candida auris, hydrolase |
Biological source | [Candida] auris |
Total number of polymer chains | 1 |
Total formula weight | 23634.14 |
Authors | Kirkman, T.J.,Dias, M.V.B. (deposition date: 2022-05-26, release date: 2023-06-14, Last modification date: 2024-02-07) |
Primary citation | Kirkman, T.,Sketcher, A.,de Morais Barroso, V.,Ishida, K.,Tosin, M.,Dias, M.V.B. Crystal structure of dihydrofolate reductase from the emerging pathogenic fungus Candida auris. Acta Crystallogr D Struct Biol, 79:735-745, 2023 Cited by PubMed Abstract: Candida auris has emerged as a global health problem with a dramatic spread by nosocomial transmission and a high mortality rate. Antifungal therapy for C. auris infections is currently limited due to widespread resistance to fluconazole and amphotericin B and increasing resistance to the front-line drug echinocandin. Therefore, new treatments are urgently required to combat this pathogen. Dihydrofolate reductase (DHFR) has been validated as a potential drug target for Candida species, although no structure of the C. auris enzyme (CauDHFR) has been reported. Here, crystal structures of CauDHFR are reported as an apoenzyme, as a holoenzyme and in two ternary complexes with pyrimethamine and cycloguanil, which are common antifolates, at near-atomic resolution. Preliminary biochemical and biophysical assays and antifungal susceptibility testing with a variety of classical antifolates were also performed, highlighting the enzyme-inhibition rates and the inhibition of yeast growth. These structural and functional data might provide the basis for a novel drug-discovery campaign against this global threat. PubMed: 37428844DOI: 10.1107/S2059798323004709 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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