| Literature DB >> 10441399 |
Abstract
SV40 large T antigen (TAg)-mediated transformation is dependent on binding to p53 and the retinoblastoma tumor suppressor protein (pRB) and inactivating their growth suppressive functions. Transformation minimally requires three regions of TAg: a C-terminal domain that mediates binding to p53; the LXCXE motif (residues 103-107), necessary for binding to pRB and the related proteins p107 and p130; and an N-terminal domain (residues 1-82) that contains homology to the J domain found in cellular DnaJ/Hsp40 molecular chaperone proteins. We have found that the N-terminal J domain of T Ag cooperates with the LXCXE motif to inactivate the growth suppressive functions of the pRB-related proteins. Copyright 1999 The International Association for Biologicals.Entities:
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Year: 1999 PMID: 10441399 DOI: 10.1006/biol.1998.0173
Source DB: PubMed Journal: Biologicals ISSN: 1045-1056 Impact factor: 1.856