| pubmed-article:7815490 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7815490 | lifeskim:mentions | umls-concept:C0178539 | lld:lifeskim |
| pubmed-article:7815490 | lifeskim:mentions | umls-concept:C1366764 | lld:lifeskim |
| pubmed-article:7815490 | lifeskim:mentions | umls-concept:C0332148 | lld:lifeskim |
| pubmed-article:7815490 | lifeskim:mentions | umls-concept:C0062529 | lld:lifeskim |
| pubmed-article:7815490 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:7815490 | pubmed:dateCreated | 1995-2-9 | lld:pubmed |
| pubmed-article:7815490 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7815490 | pubmed:abstractText | The mechanism of action of hepatitis B virus (HBV) X protein in transcriptional transactivation and in tumorigenesis remains obscure. We have used the yeast two-hybrid system to identify a cellular protein that can interact with HBV X protein. This protein, designated X-associated protein 1 (XAP-1), is a human homolog of the UV-damaged DNA-binding protein (UV-DDB) recovered from a monkey cell cDNA library. UV-DDB is presumed to be involved in DNA repair. The interaction between X protein and XAP-1 protein was verified by immunoprecipitation of yeast cell lysates expressing both proteins and by in vitro mixing with X protein expressed as a glutathione S-transferase fusion protein and XAP-1 protein either in HeLa cell extracts or synthesized by in vitro translation. We speculate that the interaction of X protein with a DNA repair protein may recruit cellular proteins to repair the partially double-stranded HBV genome or may modify cellular transcription processes. An effect on the cellular DNA repair system may explain a cofactor role for HBV in liver cancer development. | lld:pubmed |
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| pubmed-article:7815490 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7815490 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7815490 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7815490 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7815490 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:7815490 | pubmed:issn | 0022-538X | lld:pubmed |
| pubmed-article:7815490 | pubmed:author | pubmed-author:LeeT HTH | lld:pubmed |
| pubmed-article:7815490 | pubmed:author | pubmed-author:ButelJ SJS | lld:pubmed |
| pubmed-article:7815490 | pubmed:author | pubmed-author:ElledgeS JSJ | lld:pubmed |
| pubmed-article:7815490 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7815490 | pubmed:volume | 69 | lld:pubmed |
| pubmed-article:7815490 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7815490 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7815490 | pubmed:pagination | 1107-14 | lld:pubmed |
| pubmed-article:7815490 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:7815490 | pubmed:year | 1995 | lld:pubmed |
| pubmed-article:7815490 | pubmed:articleTitle | Hepatitis B virus X protein interacts with a probable cellular DNA repair protein. | lld:pubmed |
| pubmed-article:7815490 | pubmed:affiliation | Division of Molecular Virology, Baylor College of Medicine, Houston, Texas 77030. | lld:pubmed |
| pubmed-article:7815490 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7815490 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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