Source:http://linkedlifedata.com/resource/pubmed/id/18550529
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
34
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pubmed:dateCreated |
2008-8-18
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pubmed:abstractText |
The neuronal adaptor protein Fe65 is involved in brain development, Alzheimer disease amyloid precursor protein (APP) signaling, and proteolytic processing of APP. It contains three protein-protein interaction domains, one WW domain, and a unique tandem array of phosphotyrosine-binding (PTB) domains. The N-terminal PTB domain (Fe65-PTB1) was shown to interact with a variety of proteins, including the low density lipoprotein receptor-related protein (LRP-1), the ApoEr2 receptor, and the histone acetyltransferase Tip60. We have determined the crystal structures of human Fe65-PTB1 in its apo- and in a phosphate-bound form at 2.2 and 2.7A resolution, respectively. The overall fold shows a PTB-typical pleckstrin homology domain superfold. Although Fe65-PTB1 has been classified on an evolutionary basis as a Dab-like PTB domain, it contains attributes of other PTB domain subfamilies. The phosphotyrosine-binding pocket resembles IRS-like PTB domains, and the bound phosphate occupies the binding site of the phosphotyrosine (Tyr(P)) within the canonical NPXpY recognition motif. In addition Fe65-PTB1 contains a loop insertion between helix alpha2 and strand beta2(alpha2/beta2 loop) similar to members of the Shc-like PTB domain subfamily. The structural comparison with the Dab1-PTB domain reveals a putative phospholipid-binding site opposite the peptide binding pocket. We suggest Fe65-PTB1 to interact with its target proteins involved in translocation and signaling of APP in a phosphorylation-dependent manner.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
283
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
23113-20
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pubmed:meshHeading |
pubmed-meshheading:18550529-Amino Acid Sequence,
pubmed-meshheading:18550529-Crystallography, X-Ray,
pubmed-meshheading:18550529-Evolution, Molecular,
pubmed-meshheading:18550529-Humans,
pubmed-meshheading:18550529-Molecular Conformation,
pubmed-meshheading:18550529-Molecular Sequence Data,
pubmed-meshheading:18550529-Nerve Tissue Proteins,
pubmed-meshheading:18550529-Neurons,
pubmed-meshheading:18550529-Nuclear Proteins,
pubmed-meshheading:18550529-Phosphorylation,
pubmed-meshheading:18550529-Phosphotyrosine,
pubmed-meshheading:18550529-Protein Folding,
pubmed-meshheading:18550529-Protein Structure, Secondary,
pubmed-meshheading:18550529-Protein Structure, Tertiary,
pubmed-meshheading:18550529-Sequence Homology, Amino Acid,
pubmed-meshheading:18550529-Signal Transduction
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pubmed:year |
2008
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pubmed:articleTitle |
Crystal structure of the human Fe65-PTB1 domain.
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pubmed:affiliation |
Heidelberg University Biochemistry Center, INF328, D-69120 Heidelberg, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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