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| pubmed-article:7787243 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:7787243 | lifeskim:mentions | umls-concept:C0009017 | lld:lifeskim |
| pubmed-article:7787243 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:7787243 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:7787243 | pubmed:dateCreated | 1995-7-24 | lld:pubmed |
| pubmed-article:7787243 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7787243 | pubmed:abstractText | We have identified a human cDNA that is homologous to the chicken kinectin, a putative receptor for the organelle motor kinesin. The human cDNA clone hybridized to a single 4.6-kb mRNA species that codes for a protein of 156 kDa molecular mass. The predicted primary translation product contains an N-terminal transmembrane helix followed by a bipartite nuclear localization sequence and two further C-terminal leucine zipper motifs. In addition, the aminoacid sequence revealed a large region (327-1362) of predicted alpha-helical coiled coils. A monoclonal antibody CT-1 raised against a GST-kinectin fusion protein produced a perinuclear, endoplasmic reticulum-like staining pattern in diverse cell types from different species, indicating evolutionary conservation. Monoclonal antibody CT-1 and anti-chicken kinectin antibodies cross-reacted both in Western blotting and immunoprecipitation with a 160-kDa protein, confirming the antigenic identity of this 160-kDa protein with chicken kinectin. Epitope tagging studies revealed that the nuclear localization sequence motif of kinectin is not functional. Furthermore, a truncated kinesin cDNA lacking the N-terminal hydrophobic domain revealed a nonspecific cytoplasmic staining pattern. Together the data suggest that kinectin is an integral membrane protein anchored in the endoplasmic reticulum via a transmembrane domain. | lld:pubmed |
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| pubmed-article:7787243 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7787243 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7787243 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7787243 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7787243 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:7787243 | pubmed:issn | 1059-1524 | lld:pubmed |
| pubmed-article:7787243 | pubmed:author | pubmed-author:LemkeHH | lld:pubmed |
| pubmed-article:7787243 | pubmed:author | pubmed-author:KrämerBB | lld:pubmed |
| pubmed-article:7787243 | pubmed:author | pubmed-author:KrönkeMM | lld:pubmed |
| pubmed-article:7787243 | pubmed:author | pubmed-author:KruppaGG | lld:pubmed |
| pubmed-article:7787243 | pubmed:author | pubmed-author:FüttererAA | lld:pubmed |
| pubmed-article:7787243 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7787243 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:7787243 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7787243 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7787243 | pubmed:pagination | 161-70 | lld:pubmed |
| pubmed-article:7787243 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:7787243 | pubmed:year | 1995 | lld:pubmed |
| pubmed-article:7787243 | pubmed:articleTitle | Molecular cloning and characterization of human kinectin. | lld:pubmed |
| pubmed-article:7787243 | pubmed:affiliation | Institut für Medizinische Mikrobiologie und Hygiene, Technische Universität München, Germany. | lld:pubmed |
| pubmed-article:7787243 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7787243 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:7787243 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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