1HX3
CRYSTAL STRUCTURE OF E.COLI ISOPENTENYL DIPHOSPHATE:DIMETHYLALLYL DIPHOSPHATE ISOMERASE
Summary for 1HX3
Entry DOI | 10.2210/pdb1hx3/pdb |
Related | 1HZT |
Descriptor | ISOPENTENYL DIPHOSPHATE DELTA-ISOMERASE, SULFATE ION, MANGANESE (II) ION, ... (5 entities in total) |
Functional Keywords | isopentenyl, dimethylallyl, isomerase, isoprenoids |
Biological source | Escherichia coli |
Cellular location | Cytoplasm: Q46822 |
Total number of polymer chains | 2 |
Total formula weight | 43580.81 |
Authors | Durbecq, V.,Sainz, G.,Oudjama, Y.,Clantin, B.,Bompard-Gilles, C.,Tricot, C.,Caillet, J.,Stalon, V.,Droogmans, L.,Villeret, V. (deposition date: 2001-01-11, release date: 2001-07-11, Last modification date: 2024-05-29) |
Primary citation | Durbecq, V.,Sainz, G.,Oudjama, Y.,Clantin, B.,Bompard-Gilles, C.,Tricot, C.,Caillet, J.,Stalon, V.,Droogmans, L.,Villeret, V. Crystal structure of isopentenyl diphosphate:dimethylallyl diphosphate isomerase. Embo J., 20:1530-1537, 2001 Cited by PubMed Abstract: Isopentenyl diphosphate:dimethylallyl diphosphate (IPP:DMAPP) isomerase catalyses a crucial activation step in the isoprenoid biosynthesis pathway. This enzyme is responsible for the isomerization of the carbon-carbon double bond of IPP to create the potent electrophile DMAPP. DMAPP then alkylates other molecules, including IPP, to initiate the extraordinary variety of isoprenoid compounds found in nature. The crystal structures of free and metal-bound Escherichia coli IPP isomerase reveal critical active site features underlying its catalytic mechanism. The enzyme requires one Mn(2+) or Mg(2+) ion to fold in its active conformation, forming a distorted octahedral metal coordination site composed of three histidines and two glutamates and located in the active site. Two critical residues, C67 and E116, face each other within the active site, close to the metal-binding site. The structures are compatible with a mechanism in which the cysteine initiates the reaction by protonating the carbon-carbon double bond, with the antarafacial rearrangement ultimately achieved by one of the glutamates involved in the metal coordination sphere. W161 may stabilize the highly reactive carbocation generated during the reaction through quadrupole- charge interaction. PubMed: 11285217DOI: 10.1093/emboj/20.7.1530 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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