1kiz

From Proteopedia

Revision as of 18:49, 30 March 2008 by OCA (Talk | contribs)
Jump to: navigation, search


PDB ID 1kiz

Drag the structure with the mouse to rotate
, resolution 2.60Å
Ligands: , ,
Gene: Tri5 (Fusarium sporotrichioides)
Activity: Trichodiene synthase, with EC number 4.2.3.6
Related: 1JFG, 1KIY, 1JFA


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



D100E trichodiene synthase complexed with pyrophosphate


Overview

The 2.4 A resolution X-ray crystal structure of D100E trichodiene synthase and the 2.6 A resolution structure of its complex with inorganic pyrophosphate are reported. The D100E amino acid substitution in the so-called "aspartate-rich" motif does not result in large changes to the overall structure of the enzyme. In the pyrophosphate complex, however, pyrophosphate coordinates two Mg(2+) ions at the mouth of the active site without causing large changes in the structure of the enzyme. This contrasts with pyrophosphate binding in the wild-type enzyme, where pyrophosphate coordinates three Mg(2+) ions and triggers a significant conformational change that closes the mouth of the active site and optimizes packing density in the enzyme-substrate complex. The attenuation of active site closure in D100E trichodiene synthase compromises enzyme-substrate packing density and confers additional spatial and conformational degrees of freedom on the substrate and carbocation intermediates, which in turn results in the formation of five alternate sesquiterpene products in addition to trichodiene. By extension, then, the diversity of terpene cyclases in biology may have evolved in part by amino acid substitutions that fine-tune structural changes dependent on metal-diphosphate complexation that govern the formation of the active site template and enzyme-substrate packing density.

About this Structure

1KIZ is a Single protein structure of sequence from Fusarium sporotrichioides. Full crystallographic information is available from OCA.

Reference

X-ray crystal structures of D100E trichodiene synthase and its pyrophosphate complex reveal the basis for terpene product diversity., Rynkiewicz MJ, Cane DE, Christianson DW, Biochemistry. 2002 Feb 12;41(6):1732-41. PMID:11827517

Page seeded by OCA on Sun Mar 30 21:49:16 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools