Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1995 Jan 15;305 ( Pt 2)(Pt 2):499-504.
doi: 10.1042/bj3050499.

A novel receptor-type protein tyrosine phosphatase with a single catalytic domain is specifically expressed in mouse brain

Affiliations
Comparative Study

A novel receptor-type protein tyrosine phosphatase with a single catalytic domain is specifically expressed in mouse brain

W Hendriks et al. Biochem J. .

Abstract

Protein tyrosine phosphatases (PTPases) are important regulatory proteins that, together with protein tyrosine kinases, determine the phosphotyrosine levels in cell signalling proteins. By PCR amplification of mouse brain cDNA fragments encoding the catalytic domains of these enzymes, we identified three novel members of the PTPase gene family. Northern-blot analysis showed that two of these novel clones represent brain-specific PTPases, whereas the third originates from a large-sized mRNA that is more ubiquitously expressed. A full-length cDNA encoding one of the brain-specific PTPases, PTP-SL, was isolated. Sequence analysis revealed a transmembrane PTPase containing a single catalytic phosphatase domain that has 45% homology to a rat cytoplasmic brain-specific PTPase named STEP. This suggests a role for PTP-SL in cell-cell signalling processes in the brain.

PubMed Disclaimer

References

    1. Gene. 1988 Jul 15;67(1):31-40 - PubMed
    1. Blood. 1991 Nov 1;78(9):2222-8 - PubMed
    1. Mol Cell Biochem. 1992 Feb 12;109(2):107-13 - PubMed
    1. Biochem Biophys Res Commun. 1992 Jun 30;185(3):818-25 - PubMed
    1. Cell. 1992 Jul 24;70(2):225-36 - PubMed

Publication types

MeSH terms

Substances