1w19
From Proteopedia
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LUMAZINE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS BOUND TO 3-(1,3,7-TRIHYDRO-9-D-RIBITYL-2,6,8-PURINETRIONE-7-YL) PROPANE 1-PHOSPHATE
Overview
The enzymes involved in the biosynthesis of riboflavin represent, attractive targets for the development of drugs against bacterial, pathogens, because the inhibitors of these enzymes are not likely to, interfere with enzymes of the mammalian metabolism. Lumazine synthase, catalyzes the penultimate step in the riboflavin biosynthesis pathway. A, number of substituted purinetrione compounds represent a new class of, highly specific inhibitors of lumazine synthase from Mycobacterium, tuberculosis. To develop potent antibiotics for the treatment of, tuberculosis, we have determined the structure of lumazine synthase from, M. tuberculosis in complex with two purinetrione inhibitors and have, studied binding via isothermal titration calorimetry. The structures were, determined by molecular ... [(full description)]
About this Structure
1W19 is a [Single protein] structure of sequence from [Mycobacterium tuberculosis] with K, DTU, T1P, T2P, DTV, T5P, T4P, D1D and ACY as [ligands]. Active as [[1]], with EC number [2.5.1.9]. Full crystallographic information is available from [OCA].
Reference
Crystal structure of lumazine synthase from Mycobacterium tuberculosis as a target for rational drug design: binding mode of a new class of purinetrione inhibitors., Morgunova E, Meining W, Illarionov B, Haase I, Jin G, Bacher A, Cushman M, Fischer M, Ladenstein R, Biochemistry. 2005 Mar 1;44(8):2746-58. PMID:15723519
Page seeded by OCA on Mon Oct 29 19:55:47 2007
Categories: Mycobacterium tuberculosis | Single protein | Bacher, A. | Cushman, M. | Fischer, M. | Haase, I. | Illarionov, B. | Ladenstein, R. | Meining, W. | Morgunova, E. | ACY | D1D | DTU | DTV | K | T1P | T2P | T4P | T5P | Crystal structure | Inhibitor binding | Lumazine synthase | Riboflavin biosynthesis | Transferase | X-ray diffraction