Literature DB >> 9207182

Expression of a kinase-defective Eph-like receptor in the normal human brain.

H Matsuoka1, N Iwata, M Ito, M Shimoyama, A Nagata, K Chihara, S Takai, T Matsui.   

Abstract

We have identified a human Eph-family protein, HEP, gene located in human chromosomal region 7q33-->q35. The deduced amino acid sequence shared primary structural properties of Eph-family receptor tyrosine kinases. However, six invariant amino acids such as a lysine in the ATP-binding site and an aspartic acid in the phosphotransfer site of a conserved catalytic domain were substituted with other amino acid residues in HEP. Thus, no intrinsic tyrosine kinase activity was detectable in the catalytic domain expressed in CHO-K1 cell transfectants. Although most kinase-defective mutants of growth factor receptors have been reported as pathogenic receptors, its transcript was abundantly expressed in normal human adult tissues. A 135-kDa HEP protein was expressed in the human brain as much as in CHO-K1 cells transfected with a HEP cDNA expression vector. HEP is the first description of a kinase-defective Eph-family protein expressed abundantly in normal human tissues.

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Year:  1997        PMID: 9207182     DOI: 10.1006/bbrc.1997.6812

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  14 in total

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4.  Marked disturbance of calcium homeostasis in mice with targeted disruption of the Trpv6 calcium channel gene.

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Review 7.  Structural conservation of a short, functional, peptide-sequence motif.

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9.  The junction-associated protein AF-6 interacts and clusters with specific Eph receptor tyrosine kinases at specialized sites of cell-cell contact in the brain.

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10.  The EphB6 receptor is overexpressed in pediatric T cell acute lymphoblastic leukemia and increases its sensitivity to doxorubicin treatment.

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Journal:  Sci Rep       Date:  2017-11-07       Impact factor: 4.379

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