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PMID: 10889041 Published · ppublish English Journal Article

MDP-1: A novel eukaryotic magnesium-dependent phosphatase.

Biochemistry ·Vol. 39 ·No. 28 ·2000-07-18 ·Pages 8315-24

Selengut JD, Levine RL

Abstract

We report here the purification, cloning, expression, and characterization of a novel phosphatase, MDP-1. In the course of investigating the reported acid phosphatase activity of carbonic anhydrase III preparations, several discrete phosphatases were discerned. One of these, a magnesium-dependent species of 18.6 kDa, was purified to homogeneity and yielded several peptide sequences from which the parent gene was identified by database searching. Although orthologous genes were identified in fungi and plants as well as mammalian species, there was no apparent homology to any known family of phosphatases. The enzyme was expressed in Escherichia coli with a fusion tag and purified by affinity methods. The recombinant enzyme showed magnesium-dependent acid phosphatase activity comparable to the originally isolated rabbit protein. The enzyme catalyzes the rapid hydrolysis of p-nitrophenyl phosphate, ribose-5-phosphate, and phosphotyrosine. The selectivity for phosphotyrosine over phosphoserine or phosphothreonine is considerable, but the enzyme did not show activity toward five phosphotyrosine-containing peptides. None of the various substrates assayed (including various nucleotide, sugar, amino acid and peptide phosphates, phosphoinositides, and phosphodiesters) exhibited K(M) values lower than 1 mM, and many showed negligible rates of hydrolysis. The enzyme is inhibited by vanadate and fluoride but not by azide, cyanide, calcium, lithium, or tartaric acid. Chemical labeling, refolding, dialysis, and mutagenesis experiments suggest that the enzymatic mechanism is not dependent on cysteine, histidine, or nonmagnesium metal ions. In recognition of these observations, the enzyme has been given the name magnesium-dependent phosphatase-1 (MDP-1).

MeSH Terms
Amino Acid Sequence Animals Catalysis Cations Chromatography, Affinity Cloning, Molecular Cysteine/metabolism Enzyme Inhibitors/pharmacology Histidine/metabolism Hydrogen-Ion Concentration Magnesium/metabolism Mice Molecular Sequence Data Phosphoprotein Phosphatases/chemistry,genetics,metabolism Protein Phosphatase 1 Protein Phosphatase 2C Rabbits Sequence Analysis, Protein Sequence Homology, Amino Acid Substrate Specificity
Chemicals
Cations Enzyme Inhibitors Histidine Mdp1 protein, mouse Phosphoprotein Phosphatases Protein Phosphatase 1 Protein Phosphatase 2C Magnesium Cysteine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Selengut J D
Laboratory of Biochemistry, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892-0320, USA. selengut@nih.gov
Levine R L
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2000-07-18
Pages
8315-24
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Databases
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