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3UWM

Ec_IspH in complex with 4-oxobutyl diphosphate (1302)

Summary for 3UWM
Entry DOI10.2210/pdb3uwm/pdb
Related3DNF 3KE8
Descriptor4-hydroxy-3-methylbut-2-enyl diphosphate reductase, IRON/SULFUR CLUSTER, 4-oxobutyl trihydrogen diphosphate, ... (5 entities in total)
Functional Keywordscytosol, iron-sulfur protein, reductase, oxidoreductase
Biological sourceEscherichia coli
Total number of polymer chains2
Total formula weight73276.56
Authors
Span, I.,Wang, K.,Wang, W.,Zhang, Y.,Bacher, A.,Eisenreich, W.,Schulz, C.,Oldfield, E.,Groll, M. (deposition date: 2011-12-02, release date: 2012-09-05, Last modification date: 2023-09-13)
Primary citationSpan, I.,Wang, K.,Wang, W.,Zhang, Y.,Bacher, A.,Eisenreich, W.,Li, K.,Schulz, C.,Oldfield, E.,Groll, M.
Discovery of acetylene hydratase activity of the iron-sulphur protein IspH.
Nat Commun, 3:1042-1042, 2012
Cited by
PubMed Abstract: The final step of the methylerythritol phosphate isoprenoid biosynthesis pathway is catalysed by the iron-sulphur enzyme IspH, producing the universal precursors of terpenes: isopentenyl diphosphate and dimethylallyl diphosphate. Here we report an unforeseen reaction discovered during the investigation of the interaction of IspH with acetylene inhibitors by X-ray crystallography, Mößbauer, and nuclear magnetic resonance spectroscopy. In addition to its role as a 2H(+)/2e(-) reductase, IspH can hydrate acetylenes to aldehydes and ketones via anti-Markovnikov/Markovnikov addition. The reactions only occur with the oxidised protein and proceed via η(1)-O-enolate intermediates. One of these is characterized crystallographically and contains a C4 ligand oxygen bound to the unique, fourth iron in the 4Fe-4S cluster: this intermediate subsequently hydrolyzes to produce an aldehyde product. This unexpected side to IspH reactivity is of interest in the context of the mechanism of action of other acetylene hydratases, as well as in the design of antiinfectives targeting IspH.
PubMed: 22948824
DOI: 10.1038/ncomms2052
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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