pubmed-article:1280166 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C0042769 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C0014442 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C0004358 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C0205460 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C1512571 | lld:lifeskim |
pubmed-article:1280166 | lifeskim:mentions | umls-concept:C2347946 | lld:lifeskim |
pubmed-article:1280166 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:1280166 | pubmed:dateCreated | 1992-12-30 | lld:pubmed |
pubmed-article:1280166 | pubmed:abstractText | Macro enzymes, i.e. complexes of normal (iso-)enzymes with an immunoglobulin, may be due to immunological cross-reactions evoked by specific viral antigenic determinants that are homologous to regions in the target enzymes. A search of the National Biomedical Research Foundation protein databank with the amino-acid sequence of human pancreatic amylase revealed a marked homology with a fragment of the yellow fever virus major envelope protein E: i.e. an overall identity of 19.7 per cent and a high degree (40.9 per cent) of conservative amino-acid substitutions over 119 amino acids. At each identical position, the corresponding residue of Taka amylase A was examined by three-dimensional structure analysis, to determine whether the position is likely to be buried or exposed. The existence of a site (epitope) on amylase recognized by an anti-amylase antibody is discussed. | lld:pubmed |
pubmed-article:1280166 | pubmed:language | eng | lld:pubmed |
pubmed-article:1280166 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1280166 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1280166 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1280166 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1280166 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1280166 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1280166 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1280166 | pubmed:month | Aug | lld:pubmed |
pubmed-article:1280166 | pubmed:issn | 0939-4974 | lld:pubmed |
pubmed-article:1280166 | pubmed:author | pubmed-author:MulderJJ | lld:pubmed |
pubmed-article:1280166 | pubmed:author | pubmed-author:WeijersR NRN | lld:pubmed |
pubmed-article:1280166 | pubmed:author | pubmed-author:LawsonCC | lld:pubmed |
pubmed-article:1280166 | pubmed:author | pubmed-author:LeunissenJJ | lld:pubmed |
pubmed-article:1280166 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1280166 | pubmed:volume | 30 | lld:pubmed |
pubmed-article:1280166 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1280166 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1280166 | pubmed:pagination | 449-54 | lld:pubmed |
pubmed-article:1280166 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:meshHeading | pubmed-meshheading:1280166-... | lld:pubmed |
pubmed-article:1280166 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1280166 | pubmed:articleTitle | Induction of autoantibodies to human enzymes following viral infection: a biologically relevant hypothesis. | lld:pubmed |
pubmed-article:1280166 | pubmed:affiliation | Department of Clinical Chemistry, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands. | lld:pubmed |
pubmed-article:1280166 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1280166 | pubmed:publicationType | Comparative Study | lld:pubmed |