pubmed-article:1307487 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C0038409 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C0205145 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C0017772 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C0314765 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C1334043 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
pubmed-article:1307487 | lifeskim:mentions | umls-concept:C1707271 | lld:lifeskim |
pubmed-article:1307487 | pubmed:issue | 20 | lld:pubmed |
pubmed-article:1307487 | pubmed:dateCreated | 1992-11-13 | lld:pubmed |
pubmed-article:1307487 | pubmed:abstractText | The homologous C-terminal repeats of Clostridium difficile toxins (ToxA and ToxB) and streptococcal glucosyltransferases appear to mediate protein-carbohydrate interactions at cellular binding sites with sugar moieties as substrates. A consensus sequence of 134 repeating units from gram-positive bacteria indicates that these repeats have a modular design with (i) a stretch of aromatic amino acids proposed to be involved in the primary carbohydrate-protein interaction, (ii) an amplification of this interaction by repetition of the respective sequences, and (iii) a second domain, not characterized, that is responsible for carbohydrate specificity. | lld:pubmed |
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pubmed-article:1307487 | pubmed:language | eng | lld:pubmed |
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pubmed-article:1307487 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:1307487 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1307487 | pubmed:month | Oct | lld:pubmed |
pubmed-article:1307487 | pubmed:issn | 0021-9193 | lld:pubmed |
pubmed-article:1307487 | pubmed:author | pubmed-author:KuramitsuH... | lld:pubmed |
pubmed-article:1307487 | pubmed:author | pubmed-author:von... | lld:pubmed |
pubmed-article:1307487 | pubmed:author | pubmed-author:SauerbornMM | lld:pubmed |
pubmed-article:1307487 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1307487 | pubmed:volume | 174 | lld:pubmed |
pubmed-article:1307487 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1307487 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1307487 | pubmed:pagination | 6707-10 | lld:pubmed |
pubmed-article:1307487 | pubmed:dateRevised | 2010-9-7 | lld:pubmed |
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pubmed-article:1307487 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1307487 | pubmed:articleTitle | Evidence for a modular structure of the homologous repetitive C-terminal carbohydrate-binding sites of Clostridium difficile toxins and Streptococcus mutans glucosyltransferases. | lld:pubmed |
pubmed-article:1307487 | pubmed:affiliation | Institut für Medizinische Mikrobiologie, Johannes-Gutenberg-Universität, Mainz, Federal Republic of Germany. | lld:pubmed |
pubmed-article:1307487 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1307487 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:1307487 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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