Literature DB >> 9169026

Selenophosphate synthetase: enzyme labeling studies with [gamma-32P]ATP, [beta-32P]ATP, [8-14C]ATP, and [75Se]selenide.

S Y Liu1, T C Stadtman.   

Abstract

Selenophosphate synthetase catalyzes a reaction in which ATP and selenide are converted to H3SeP03, H3P04, and AMP in a 1:1:1 ratio. Selenophosphate is derived from the gamma phosphoryl group and orthophosphate from the beta phosphoryl group of ATP. In the absence of selenide, a slow reaction in which ATP is converted quantitatively to 2 H3P04 and AMP occurs. Labeling experiments carried out to detect a putative enzyme-bound pyrophosphate intermediate in the overall reaction showed that up to 0.6 equivalent of the 32P label from [gamma-32P]ATP was bound to protein under enzyme turnover conditions, but only a negligible amount of 32P from [beta-32P]ATP was present. Thus, no Enz-PP intermediate was present in a detectable amount under the experimental conditions used. Isolated enzyme samples contained 75Se from 75Se-labeled selenide and [14C]AMP from [8-14C]ATP in amounts similar to the bound 32P from [gamma-32P]ATP, suggesting that two of the final products, selenophosphate and AMP, were the radioactive compounds detected in these experiments.

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Year:  1997        PMID: 9169026     DOI: 10.1006/abbi.1997.9990

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  3 in total

1.  Isotope exchange studies on the Escherichia coli selenophosphate synthetase mechanism.

Authors:  H Walker; J A Ferretti; T C Stadtman
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-03       Impact factor: 11.205

2.  Structure of an N-terminally truncated selenophosphate synthetase from Aquifex aeolicus.

Authors:  Eiko Matsumoto; Shun Ichi Sekine; Ryogo Akasaka; Yumi Otta; Kazushige Katsura; Mio Inoue; Tatsuya Kaminishi; Takaho Terada; Mikako Shirouzu; Shigeyuki Yokoyama
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2008-05-16

3.  Biochemical discrimination between selenium and sulfur 1: a single residue provides selenium specificity to human selenocysteine lyase.

Authors:  Ruairi Collins; Ann-Louise Johansson; Tobias Karlberg; Natalia Markova; Susanne van den Berg; Kenneth Olesen; Martin Hammarström; Alex Flores; Herwig Schüler; Lovisa Holmberg Schiavone; Peter Brzezinski; Elias S J Arnér; Martin Högbom
Journal:  PLoS One       Date:  2012-01-25       Impact factor: 3.240

  3 in total

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