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3UTD

Ec_IspH in complex with 4-oxopentyl diphosphate

Summary for 3UTD
Entry DOI10.2210/pdb3utd/pdb
Related3DNF 3KE8 3UTC 3UV3 3UV6 3UV7 3UV8 3UWM 3urk
Descriptor4-hydroxy-3-methylbut-2-enyl diphosphate reductase, FE3-S4 CLUSTER, 4-oxopentyl trihydrogen diphosphate, ... (4 entities in total)
Functional Keywordsiron-sulfur protein, isph, lytb, isoprenoid biosynthesis, non-mevalonate pathway, oxidoreductase
Biological sourceEscherichia coli
Total number of polymer chains2
Total formula weight72696.80
Authors
Span, I.,Wang, K.,Wang, W.,Zhang, Y.,Bacher, A.,Eisenreich, W.,Schulz, C.,Oldfield, E.,Groll, M. (deposition date: 2011-11-25, 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 (1.7 Å)
Structure validation

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