pubmed-article:18791240 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0521390 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0051926 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0950625 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0733755 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0150305 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C1561964 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C1416769 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0162610 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:18791240 | lifeskim:mentions | umls-concept:C1314677 | lld:lifeskim |
pubmed-article:18791240 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:18791240 | pubmed:dateCreated | 2008-11-12 | lld:pubmed |
pubmed-article:18791240 | pubmed:abstractText | The L1 family of single-pass transmembrane cell adhesion molecules (L1CAMs) is conserved from Caenorhabditis elegans and Drosophila to vertebrates and is required for axon guidance, neurite outgrowth, and maintenance of neuronal positions. The extracellular region of L1CAMs mediates cell adhesion via interactions with diverse cell-surface and extracellular matrix proteins. In contrast, less is known regarding the function of the intracellular domains in the L1CAM cytoplasmic tail. Previously, we identified a role of the C. elegans L1CAM homolog, SAX-7, in maintaining neuronal and axonal positioning. Here, we demonstrate that this function is dependent on three conserved motifs that reside in the SAX-7 cytoplasmic tail: (1) the FERM-binding motif, (2) the ankyrin-binding domain, and (3) the PDZ-binding motif. Furthermore, we provide molecular and genetic evidence that UNC-44 ankyrin and STN-2 gamma-syntrophin bind SAX-7 via the respective ankyrin-binding and PDZ-binding motifs to regulate SAX-7 function in maintaining neuronal positioning. | lld:pubmed |
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pubmed-article:18791240 | pubmed:language | eng | lld:pubmed |
pubmed-article:18791240 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18791240 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18791240 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18791240 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:18791240 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:18791240 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18791240 | pubmed:month | Nov | lld:pubmed |
pubmed-article:18791240 | pubmed:issn | 0016-6731 | lld:pubmed |
pubmed-article:18791240 | pubmed:author | pubmed-author:ZhouShanS | lld:pubmed |
pubmed-article:18791240 | pubmed:author | pubmed-author:WangXuelinX | lld:pubmed |
pubmed-article:18791240 | pubmed:author | pubmed-author:ChenLihsiaL | lld:pubmed |
pubmed-article:18791240 | pubmed:author | pubmed-author:OppermanKarla... | lld:pubmed |
pubmed-article:18791240 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18791240 | pubmed:volume | 180 | lld:pubmed |
pubmed-article:18791240 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18791240 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18791240 | pubmed:pagination | 1429-43 | lld:pubmed |
pubmed-article:18791240 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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