| pubmed-article:3004934 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0009498 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C1622637 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0009017 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0427579 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0441509 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C1704666 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C1517892 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0073906 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0141319 | lld:lifeskim |
| pubmed-article:3004934 | lifeskim:mentions | umls-concept:C0208973 | lld:lifeskim |
| pubmed-article:3004934 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:3004934 | pubmed:dateCreated | 1986-4-23 | lld:pubmed |
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| pubmed-article:3004934 | pubmed:abstractText | cDNA clones coding for human S-protein have been isolated using monoclonal antibodies to screen a cDNA library in pEX. These clones are shown to be authentic S-protein clones on the basis of sequence, composition and immunological criteria. The complete open reading frame sequence for S-protein has been determined and shows it to be a single polypeptide chain of 459 amino acids preceded by a cleaved leader peptide of 19 residues. No evidence was found for polymorphism of S-protein suggesting that different molecular weight forms arise by proteolytic degradation. Of the first 44 amino-terminal residues 42 are identical with the so-called somatomedin B peptide suggesting that S-protein is the somatomedin B precursor. Striking homology is found in the rest of the sequence with the serum spreading factor, vitronectin, which has also been shown to contain somatomedin B sequences at its amino terminus. We conclude that S-protein and vitronectin are identical and discuss the relevance of this finding to the coagulation and complement pathways. | lld:pubmed |
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| pubmed-article:3004934 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:3004934 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3004934 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3004934 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:3004934 | pubmed:issn | 0261-4189 | lld:pubmed |
| pubmed-article:3004934 | pubmed:author | pubmed-author:StanleyK KKK | lld:pubmed |
| pubmed-article:3004934 | pubmed:author | pubmed-author:JennyPP | lld:pubmed |
| pubmed-article:3004934 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3004934 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:3004934 | pubmed:volume | 4 | lld:pubmed |
| pubmed-article:3004934 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3004934 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3004934 | pubmed:pagination | 3153-7 | lld:pubmed |
| pubmed-article:3004934 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:3004934 | pubmed:year | 1985 | lld:pubmed |
| pubmed-article:3004934 | pubmed:articleTitle | Molecular cloning of S-protein, a link between complement, coagulation and cell-substrate adhesion. | lld:pubmed |
| pubmed-article:3004934 | pubmed:publicationType | Journal Article | lld:pubmed |
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