Src homology 2 and 3 regions of p120 kDa rasGTPase activating protein induces morphological alteration of rat 3Y1 fibroblast

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dc.contributor.authorJong-Soo Chang-
dc.contributor.authorKi Hong Yoon-
dc.contributor.authorM Kobayashi-
dc.contributor.authorS Iwashita-
dc.date.accessioned2017-04-19T08:44:57Z-
dc.date.available2017-04-19T08:44:57Z-
dc.date.issued1995-
dc.identifier.issn1016-8478-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3591-
dc.description.abstractpl20 kDa rasGTPase activating protein (GAP), as a negative regulator of pH™5, contains src homology (SH) 2 and 3 regions just upstream of catalytic domain, which has no GTPase activity but it stimulates GTPase activity of normal c-ras gene product To investigate the differential role of non-catalytic regulatory domain of GAP in cell growth control,we constructed a truncated gene encoding 164-449 amino acids of rat GAP which correspond to SH2/SH3 re없on alone and expressed in rat fibroblast using stable mammalian expression vector. Expression of only SH2/SH3 re建on of GAP in 3Y1 cells resulted in a morphological alterations. Furthermore, this SH2/SH3 re建on expressing clones showed increased phosphotyrosine levels of pl90 and p62 when those cells were incubated in orthovanadate, a protein phosphatase inhibitor. These results suggest that src homology regions of pl20 kDa GAP have a unique biological activity in cellular signaling.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleSrc homology 2 and 3 regions of p120 kDa rasGTPase activating protein induces morphological alteration of rat 3Y1 fibroblast-
dc.title.alternativeSrc homology 2 and 3 regions of p120 kDa rasGTPase activating protein induces morphological alteration of rat 3Y1 fibroblast-
dc.typeArticle-
dc.citation.titleMolecules and Cells-
dc.citation.number1-
dc.citation.endPage51-
dc.citation.startPage47-
dc.citation.volume5-
dc.contributor.affiliatedAuthorKi Hong Yoon-
dc.contributor.alternativeName장종수-
dc.contributor.alternativeName윤기홍-
dc.contributor.alternativeNameKobayashi-
dc.contributor.alternativeNameIwashita-
dc.identifier.bibliographicCitationMolecules and Cells, vol. 5, no. 1, pp. 47-51-
dc.description.journalClassY-
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