2g8h
From Proteopedia
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B. halodurans RNase H catalytic domain D192N mutant in complex with Mg2+ and RNA/DNA hybrid (non-P nick at the active site)
Overview
In two-metal catalysis, metal ion A has been proposed to activate the, nucleophile and metal ion B to stabilize the transition state. We recently, reported crystal structures of RNase H-RNA/DNA substrate complexes, obtained at 1.5-2.2 Angstroms. We have now determined and report here, structures of reaction intermediate and product complexes of RNase H at, 1.65-1.85 Angstroms. The movement of the two metal ions suggests how they, may facilitate RNA hydrolysis during the catalytic process. Firstly, metal, ion A may assist nucleophilic attack by moving towards metal ion B and, bringing the nucleophile close to the scissile phosphate. Secondly, metal, ion B transforms from an irregular coordination in the substrate complex, to a more regular geometry in the product complex. The exquisite, sensitivity of Mg(2+) to the coordination environment likely destabilizes, the enzyme-substrate complex and reduces the energy barrier to form, product. Lastly, product release probably requires dissociation of metal, ion A, which is inhibited by either high concentrations of divalent, cations or mutation of an assisting protein residue.
About this Structure
2G8H is a Single protein structure of sequence from Bacillus halodurans with MG and VO4 as ligands. Active as Ribonuclease H, with EC number 3.1.26.4 Full crystallographic information is available from OCA.
Reference
Stepwise analyses of metal ions in RNase H catalysis from substrate destabilization to product release., Nowotny M, Yang W, EMBO J. 2006 May 3;25(9):1924-33. Epub 2006 Apr 6. PMID:16601679
Page seeded by OCA on Wed Nov 21 11:01:51 2007
Categories: Bacillus halodurans | Ribonuclease H | Single protein | Nowotny, M. | Yang, W. | MG | VO4 | Ribonuclease h | Rna/dna hybrid | Rnase h
