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1H48

The structure of 2C-Methyl-D-erythritol 2,4-cyclodiphosphate synthase in complex with CMP and product

Summary for 1H48
Entry DOI10.2210/pdb1h48/pdb
Related1GX1 1H47 1JY8 1KNJ 1KNK
Descriptor2C-METHYL-D-ERYTHRITOL-2,4-CYCLODIPHOSPHATE SYNTHASE, 2C-METHYL-D-ERYTHRITOL 2,4-CYCLODIPHOSPHATE, ZINC ION, ... (7 entities in total)
Functional Keywordssynthase, isoprenoid, lyase, isoprene biosynthesis
Biological sourceESCHERICHIA COLI
Total number of polymer chains6
Total formula weight107715.31
Authors
Kemp, L.E.,Alphey, M.S.,Bond, C.S.,Hunter, W.N. (deposition date: 2003-02-24, release date: 2004-12-22, Last modification date: 2023-12-13)
Primary citationKemp, L.E.,Alphey, M.S.,Bond, C.S.,Ferguson, M.,Hecht, S.,Bacher, A.,Eisenreich, W.,Rohdich, F.,Hunter, W.N.
The Identification of Isoprenoids that Bind in the Intersubunit Cavity of Escherichia Coli 2C-Methyl-D-Erythritol-2,4-Cyclodiphosphate Synthase by Complementary Biophysical Methods
Acta Crystallogr.,Sect.D, 61:45-, 2005
Cited by
PubMed Abstract: The discovery of a distinct metabolic pathway, the non-mevalonate or 1-deoxy-D-xylulose-5-phosphate (DOXP) pathway for isoprenoid precursor biosynthesis, in eubacteria and apicomplexan parasites has revealed a new set of potential drug targets. The emphasis of research on this pathway has been on delineating the intermediates and the biochemical and structural characterization of component enzymes. Two new monoclinic crystal forms of recombinant Escherichia coli 2C-methyl-D-erythritol-2,4-cyclodiphosphate (MECP) synthase cocrystallized with (i) CMP and (ii) CMP and MECP show well defined electron density at the subunit interface suggestive of an isoprenoid-like ligand. 31P NMR analysis of the recombinant protein sample indicates the presence of bound diphosphate species and electrospray mass spectrometry identifies a mixture of isopentenyl diphosphate (and/or dimethylallyl diphosphate), geranyl diphosphate and farnesyl diphosphate in an approximate ratio of 1:4:2. The most prevalent species, geranyl diphosphate, was successfully modelled into the electron density, revealing the important protein-ligand interactions that stabilize binding of the isoprenoid. The observation that MECP synthase binds three metabolites that are produced by enzymes two, three and four stages downstream in isoprenoid biosynthesis suggests that feedback regulation of the non-mevalonate pathway is possible.
PubMed: 15608374
DOI: 10.1107/S0907444904025971
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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