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2JFB

3D Structure of Lumazine Synthase from Candida albicans

Summary for 2JFB
Entry DOI10.2210/pdb2jfb/pdb
Descriptor6,7-DIMETHYL-8-RIBITYLLUMAZINE SYNTHASE, PHOSPHATE ION, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (4 entities in total)
Functional Keywordstransferase, candida albicans, lumazine synthase, riboflavin biosynthesis
Biological sourceCANDIDA ALBICANS
Total number of polymer chains15
Total formula weight274181.14
Authors
Morgunova, E.,Fischer, M.,Cushman, M.,Bacher, A.,Ladenstein, R. (deposition date: 2007-01-30, release date: 2007-05-01, Last modification date: 2023-12-13)
Primary citationMorgunova, E.,Saller, S.,Haase, I.,Cushman, M.,Bacher, A.,Fischer, M.,Ladenstein, R.
Lumazine Synthase from Candida Albicans as an Anti- Fungal Target Enzyme: Structural and Biochemical Basis for Drug Design.
J.Biol.Chem., 282:17231-, 2007
Cited by
PubMed Abstract: Lumazine synthase is an enzyme involved in riboflavin biosynthesis in many plants and microorganisms, including numerous human pathogens. The fact that the enzymes of the riboflavin biosynthesis pathway are not present in the human or animal host makes them potential targets for anti-infective agents. The crystal structure of lumazine synthase from Candida albicans was solved by molecular replacement and refined at 2.5-Angstrom resolution. The results of crystallographic investigations and sedimentation equilibrium experiments clearly indicated the presence of pentameric assemblies of the enzyme either in crystals or in solution. Isothermal titration calorimetry measurements of the binding reactions of four different inhibitors revealed high affinity for all four compounds with binding constants in the micromolar range. Structural comparison with previously determined structures of the enzyme.ligand complexes of other orthologue allowed modeling of the binding of four different inhibitors into the active site of lumazine synthase from Candida albicans.
PubMed: 17446177
DOI: 10.1074/JBC.M701724200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

237735

数据于2025-06-18公开中

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