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The cloning and sequence of the C isoform of PtdIns4P 5-kinase

The cloning and sequence of the C isoform of PtdIns4P 5-kinase
The cloning and sequence of the C isoform of PtdIns4P 5-kinase
In this study we describe the purification and sequencing of the C isoform of platelet PtdIns4P 5-kinase. Subsequently a cDNA was isolated from a human circulating-leucocyte library, which when sequenced was shown to contain all of the peptides identified in the purified protein. In addition, expression of this cDNA in bacteria led to the production of a protein which was recognized by specific monoclonal antibodies raised to the bovine brain enzyme [Brooksbank, Hutchings, Butcher, Irvine and Divecha (1993) Biochem. J. 291, 77-82] and also led to the appearance of PtdIns4P 5-kinase activity in the bacterial lysates. Interestingly, the cDNA showed no similarity to any of the previously cloned inositide kinases. A search of the DNA databases showed that two proteins from Saccharomyces cerevisiae shared close similarity to this enzyme, one of which, the mss4 gene product, has been implicated in the yeast inositol lipid pathway. These data suggest that the PtdIns4P 5-kinases are a new family of inositide kinases unrelated to the previously cloned phosphoinositide 3/4-kinases.
0264-6021
715-719
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Truong, O.
72b596b6-a7f7-4107-8c03-f26dffeb33b5
Hsuan, J. J.
3ec0f0ba-a5f1-4660-8af2-583efb0aeb92
Hinchliffe, Katherine A.
2a02065f-04cf-49bc-9ff6-da0030f3ed2f
Irvine, Robin F.
a8a94b1b-419c-4262-b745-eae1941ce145
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Truong, O.
72b596b6-a7f7-4107-8c03-f26dffeb33b5
Hsuan, J. J.
3ec0f0ba-a5f1-4660-8af2-583efb0aeb92
Hinchliffe, Katherine A.
2a02065f-04cf-49bc-9ff6-da0030f3ed2f
Irvine, Robin F.
a8a94b1b-419c-4262-b745-eae1941ce145

Divecha, N., Truong, O., Hsuan, J. J., Hinchliffe, Katherine A. and Irvine, Robin F. (1995) The cloning and sequence of the C isoform of PtdIns4P 5-kinase. Biochemical Journal, 309 (3), 715-719. (doi:10.1042/bj3090715).

Record type: Article

Abstract

In this study we describe the purification and sequencing of the C isoform of platelet PtdIns4P 5-kinase. Subsequently a cDNA was isolated from a human circulating-leucocyte library, which when sequenced was shown to contain all of the peptides identified in the purified protein. In addition, expression of this cDNA in bacteria led to the production of a protein which was recognized by specific monoclonal antibodies raised to the bovine brain enzyme [Brooksbank, Hutchings, Butcher, Irvine and Divecha (1993) Biochem. J. 291, 77-82] and also led to the appearance of PtdIns4P 5-kinase activity in the bacterial lysates. Interestingly, the cDNA showed no similarity to any of the previously cloned inositide kinases. A search of the DNA databases showed that two proteins from Saccharomyces cerevisiae shared close similarity to this enzyme, one of which, the mss4 gene product, has been implicated in the yeast inositol lipid pathway. These data suggest that the PtdIns4P 5-kinases are a new family of inositide kinases unrelated to the previously cloned phosphoinositide 3/4-kinases.

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Published date: 1995

Identifiers

Local EPrints ID: 480087
URI: http://eprints.soton.ac.uk/id/eprint/480087
ISSN: 0264-6021
PURE UUID: 37d6825c-1589-4879-9bab-fc3d544ff447

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Date deposited: 01 Aug 2023 16:46
Last modified: 17 Mar 2024 02:59

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Contributors

Author: N. Divecha
Author: O. Truong
Author: J. J. Hsuan
Author: Katherine A. Hinchliffe
Author: Robin F. Irvine

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