117e

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Image:117e.gif

117e, resolution 2.15Å

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THE R78K AND D117E ACTIVE SITE VARIANTS OF SACCHAROMYCES CEREVISIAE SOLUBLE INORGANIC PYROPHOSPHATASE: STRUCTURAL STUDIES AND MECHANISTIC IMPLICATIONS

Overview

We have solved the structure of two active-site variants of soluble, inorganic pyrophosphatases (PPase), R78K and D117K, at resolutions of 1.85, and 2.15 A and R-factors of 19.5% and 18.3%, respectively.In the R78K, variant structure, the high-affinity phosphate group (P1) is missing, consistent with the wild-type structure showing a bidentate interaction, between P1 and Arg78, and solution data showing a decrease in P1 affinity, in the variant. The structure explains why the mutation affects ... [(full description)]

About this Structure

117E is a [Protein single] structure of sequence from [SACCHAROMYCES CEREVISIAE] with MN and PO4 as [ligands].

Reference

The R78K and D117E active-site variants of Saccharomyces cerevisiae soluble inorganic pyrophosphatase: structural studies and mechanistic implications., Tuominen V, Heikinheimo P, Kajander T, Torkkel T, Hyytia T, Kapyla J, Lahti R, Cooperman BS, Goldman A, J Mol Biol. 1998 Dec 18;284(5):1565-80. PMID:9878371

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