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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
2000-1-13
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pubmed:databankReference |
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pubmed:abstractText |
The SH2-B protein is an SH2-domain-containing molecule that interacts with a number of phosphorylated kinase and receptor molecules including the insulin receptor. Two isoforms of the SH2-B have been identified and have been proposed to arise through alternate splicing. Here we have identified a third isoform of the SH2-B protein, SH2-Bgamma, that interacts specifically with the insulin receptor. This interaction required phosphorylation of residue Y1146 in the triple tyrosine motif within the activation loop of the IR kinase and is one of only two signaling molecules shown to interact directly with this residue of the insulin receptor kinase domain. The intron/exon structure of the SH2-B gene was determined. Alternate splice sites utilized to generate the different isoforms of the SH2-B protein were identified in the 3' end of the SH2-B gene immediately downstream of the exon encoding the core of the SH2 domain. Additionally, the chromosomal location of the SH2-B gene was determined to be the distal arm of mouse Chromosome (Chr) 7 in a region linked to obesity in mice.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphotyrosine,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Sh2bpsm1 protein, mouse
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0938-8990
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1160-7
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10594240-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:10594240-Alternative Splicing,
pubmed-meshheading:10594240-Amino Acid Sequence,
pubmed-meshheading:10594240-Animals,
pubmed-meshheading:10594240-Base Sequence,
pubmed-meshheading:10594240-Carrier Proteins,
pubmed-meshheading:10594240-Chromosome Mapping,
pubmed-meshheading:10594240-Cloning, Molecular,
pubmed-meshheading:10594240-Exons,
pubmed-meshheading:10594240-Introns,
pubmed-meshheading:10594240-Mice,
pubmed-meshheading:10594240-Mice, Inbred C57BL,
pubmed-meshheading:10594240-Molecular Sequence Data,
pubmed-meshheading:10594240-Molecular Weight,
pubmed-meshheading:10594240-Phosphorylation,
pubmed-meshheading:10594240-Phosphotyrosine,
pubmed-meshheading:10594240-Protein Binding,
pubmed-meshheading:10594240-Protein Isoforms,
pubmed-meshheading:10594240-RNA, Messenger,
pubmed-meshheading:10594240-Receptor, Insulin,
pubmed-meshheading:10594240-Two-Hybrid System Techniques,
pubmed-meshheading:10594240-src Homology Domains
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pubmed:year |
1999
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pubmed:articleTitle |
Alternative splicing, gene localization, and binding of SH2-B to the insulin receptor kinase domain.
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pubmed:affiliation |
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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